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==Classification==
{| class="wikitable"
'''Classification of [[breast lumps]] based on [[epithelial hyperplasia]]<ref name="pmid16034008">{{cite journal| author=Hartmann LC, Sellers TA, Frost MH, Lingle WL, Degnim AC, Ghosh K et al.| title=Benign breast disease and the risk of breast cancer. | journal=N Engl J Med | year= 2005 | volume= 353 | issue= 3 | pages= 229-37 | pmid=16034008 | doi=10.1056/NEJMoa044383 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16034008 }} </ref>'''
! Disease Name
*Approximately 65% of all benign breast disease considered as [[nonproliferative]](NP)with relative cancer risk of 1.2, 1.4 times:
! History and Symptoms
**Simple cyst
! Physical Examination
**Fibrosis
! Lab Findings
** Fibroadenoma (simple)
! Imaging Findings
** Columnar alteration (Simple)
! Gross and Histologic Findings
** Apocrine metaplasia (simple)
! Genetic Studies / Immunohistochemistry
** Mild ductal hyperplasia  
|-
* Approximately 30% of total are classifed as [[proliferative disease]](PD) with relative cancer risk of 1.7, 2.1 times
| colspan="7" style="background: #4479BA; width: 50px;" |{{fontcolor|#FFF|'''Germ Cell Tumors'''}}
** Usual ductal hyperplasia
|-
**  Sclerosing adenosis
| align="center" |
** Columnar hyperplasia
'''[[Seminoma]]'''
** papilloma
| valign="top" |
** Radical scar
*Most common
* Approximately 5% to 8% of the rest regarded to [[PD with atypia]] with relative cancer risk more than 4 times
*30-50 year-old with painless unilateral testicular mass or mild discomfort
** Atypical lobar hyperplasia
| valign="top" |
** Lobular carcinoma in situ
*Palpable, nontender unilateral testicular mass
** Atypical ductal hyperplasia
*Usually homogeneous enlargement
* Unclear risk
| valign="top" |
** Mucocele like tumor
*Elevated serum placental ALP (PALP)
** Apocrine atypia
| valign="top" |
** Secretory atypia
*Hypoechogenic intratesticular well-defined mass on ultrasound with internal blood flow on Doppler ultrasound
'''Classification of [[benign breast lesion]] regarding to [[histological region]]''':<ref>{{cite book | last = Lanyi | first = M | title = Mammography : diagnosis and pathological analysis | publisher = Springer-Verlag | location = Berlin New York | year = 2003 | isbn = 9783540441137 }}</ref>
*Cysts and calcificications are uncommon
*Terminal and lobular ducts
*Hypointense lesion with inhomogeneous enhancement on MRI
**Acinar distention
*Homogeneous when small and heterogeneous when large
***Cyst
| valign="top" |
**Intralobular connective tissue proliferation
*Grey-white homogeneous mass with a lobular appearance
***Sclerosing adenosis
*Fried egg appearance on histopathology (large cells and clear cytoplasm)
***Fibroadenoma
*Prominent lymphocytic infiltration and less commonly, granulomatous  formation
***Phyllodes tumor
| valign="top" |
***Hamartoma
*Stains positively for ALP, c-KIT, CD30, EMA, and glycogen
**Epithelial changes in terminal duct lobaular units (TDLU)
|-
***Apocrine metaplasia
| align="center" |
***Ductal and lobular hyperplasia, usual and typical
'''[[germ cell tumor|Embryonal cell carcinoma]]'''
***Papillomatosis
| valign="top" |
***Intracystic papilloma
*Young adults
*Ductal system
*Painful testicular mass
**Ductal ectasia
*Manifests with early mestastasis (bone, lung, CNS)
**Intraductal papilloma
| valign="top" |
*Lesion of different origin
* Often unremarkable (small primary tumor)
**Fatty tissue lesion
| valign="top" |
***Lipoma
*Elevated serum hCG
***Liponecrosis
*Elevated serum AFP, when mixed
**Fibrous tissue lesions
| valign="top" |
***Focal fibrosis
*Variable echogenicity (usually hypoechoic on ultrasound)
***Diabetic mastopathy
*No differentiating features on imaging
***Pseudoangiomatous stromal hyperplasia (PASH)
*Commonly invade the surrounding structures (tunica albuginea)
***Myofibroblastoma
*Irregular calcifications
**Vascular origin
| valign="top" |
***Hemangioma
*Pale-grey mass with areas of hemorrhagic and necrosis
**Inflammatory origin
*Often mixed histopathological features (solid, papillary, tubular, pseudoglandular)
***Mastitis/abscess
| valign="top" |
***Tuberclosis and sarcoidosis
*Stains positively for CD30 and hCG stain
***Foreign body granuloma and siliconoma
*May stain positively for AFP, when mixed
**Lymph node origin
|-
***Inflammatory lymoh nodes
| align="center" |
'''[[Yolk sac tumor]]'''
| valign="top" |
* Most common testicular cancer in children less than 3 years of age
*Rapidly growing unilateral mass in an infant or a young child
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Usually heterogeneous enlargement
| valign="top" |
*Elevated serum AFP
| valign="top" |
*Diffuse enlargement of the testis with a heterogeneous appearance on ultrasound
*Areas of hemorrhage and necrosis on MRI
| valign="top" |
*Yellow, mucinous, non-encapsulated, heterogeneous mass with areas of necrosis and hemorrhage
*Patterns that resemble embryonal structures (yolk sac, allantois) with reticular, papillary, or elongated forms
*Schiller-Duval bodies (perivascular structures)
| valign="top" |
*Stains positively for AFP, alpha-1-antitrypsin, PAS diastase
|-
| align="center" |
'''[[Teratoma]]'''
| valign="top" |
*Bimodal distribution of age (infants and middle aged adults)
*Painless tumor
*History of congenital disease (Down syndrome, klinefelter, spina bifida)
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Usually heterogeneous enlargement
| valign="top" |
*Elevated serum hCG
*Elevated serum AFP
| valign="top" |
*Heterogeneous, cystic appearance with mucinous or sebaceous depositions
*Variable echogenicity on ultrasound
*Calcifications usually irregular
| valign="top" |  
*Large, heterogeneous appearance with solid, cystic, mucoid, and/or cartilageanous components
*Presence of at least 2 germ layers
| valign="top" |
*Chromosome 12p mutations
*Stains positively for cytokeratin. hCG, and AFP
|-
| align="center" |
'''[[teratoma|Teratocarcinoma]] '''
| valign="top" |
*Middle aged adult with painless testicular mass of mild discomfort
*May manifest with features of metastasis
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Usually heterogeneous enlargement
| valign="top" | 
*Elevated serum hCG
*Elevated serum AFP
| valign="top" |
*Variable echogenicity on ultrasound
| valign="top" | 
*Features of both teratoma and embryonal carcinoma (more common) or both teratoma and choriocarcinoma (less common)
*Solid and cystic components with mucoid, cartilagenous, sebaceous gland, myxoid stroma components
*Additional features of underlying embryonal carcinoma or choriocarcinoma
| valign="top" | 
*Stains positively for cytokeratin. hCG, AFP, and CD30
|-
| align="center" |
'''[[Choriocarcinoma]]'''
| valign="top" |
*Adolescent or young adult with extratesticular symptoms
*Mass is small and locally asymptomatic
*Manifests with early metastasis and signs of hemorrhage  (hemorrhagic stroke, hyperthyroidism, cannon-ball metastasis in lung, liver involvement, neurological deficits)
| valign="top" |
*Often unremarkable (small primary tumor)
| valign="top" |
*Elevated serum hCG
| valign="top" |
*Variable echogenicity
*No differentiating features on imaging
*Commonly invade the surrounding structures (tunica albuginea)
| valign="top" |
*Prominent areas of hemorrhage and necrosis
*Nest and sheet pattern that simultaneously includes both cytotrophoblast and syncytiotrophoblast (rarely pure)
*Paucity of intermediate trophoblasts (unlike placental site trophoblastic tumor) 
| valign="top" |
*Stains positively for hCG
|-
| align="center" |
'''[[Germ cell tumor|Diffuse embryoma]]'''
| valign="top" |
*20-25 yo man with painful testicular mass 
| valign="top" |
*Tender testicular mass 
| valign="top" |
*Elevated serum hCG
*Elevated serum AFP
| valign="top" |
*Poorly-defined, heterogeneous hyperechoic mass on ultrasound
| valign="top" |
*Non-encapsulated mass
*Intermingled (lace-like) embryonal carcinoma and yolk sac components in equal proportions, but no discrete embyoid bodies
*Scattered trophoblastic components
*Necklace-like arrangement of cells
| valign="top" |
*Stains positively for cytokeratin, AFP (yolk sac component), and CD30 (embyonal component)
|-
| align="center" |
'''[[Polyembryoma]]'''
| valign="top" |
*20-25 yo man with painful testicular mass 
| valign="top" |
*Tender testicular mass 
| valign="top" |
*Elevated serum AFP
*Elevated serum hCG 
| valign="top" |
*Poorly-defined, heterogeneous hyperechoic mass on ultrasound 
| valign="top" |
*Multiple discrete embyoid bodies (combination of both embryonal carcinoma and yolk sac components) 
| valign="top" |
*Stains positively for cytokeratin, AFP (yolk sac component), and CD30 (embyonal component)
|-
| align="center" |
'''[[Placental site trophoblastic tumor]]'''
| valign="top" |
*Infant or young adult
*Painful small testicular mass
| valign="top" |
*Small nontender or minimally painful testicular mass 
| valign="top" |
*Elevated serum hCG 
| valign="top" |
*Variable echogenicity
*No differentiating features on imaging
*May have vascular flow 
| valign="top" |
*Solid yellowish mass that resembles uterine tissue
*Less prominent foci of hemorrhage and ncerosis
*Predominance of intermediate trophoblast cells (implantation-site type) that invade surrounding blood vessels
*Paucity of cytotrophoblast and syncytiotrophoblast cells (unlike choriocarcinoma) 
| valign="top" |
*Stains positively for hPL (diffuse), cytokeratin, AFP, and hCG (patchy)
*Negative p63 staining 
|-
| align="center" |
'''[[Epithelioid trophoblastic tumor]]'''
| valign="top" |
*Infant or young adult
*Painful small testicular mass
| valign="top" |
*Small nontender or minimally painful testicular mass 
| valign="top" |
*Elevated serum hCG 
| valign="top" |
*Variable echogenicity
*No differentiating features on imaging
*May have vascular flow 
| valign="top" |
*Solid yellowish mass that resembles uterine tissue
*Less prominent foci of hemorrhage and ncerosis
*Predominance of intermediate trophoblast cells (implantation-site type) that invade surrounding blood vessels
*Paucity of cytotrophoblast and syncytiotrophoblast cells (unlike choriocarcinoma) 
| valign="top" |
*Stains positively for p63 (diffuse), p63, cytokeratin, AFP, and hCG (patchy)
*Negative hPL staining
|-
| align="center" |
'''[[germ cell tumor|Mixed germ cell tumor]]'''
| valign="top" |
*Typical age at diagnosis and other clinical features based on underlying components
| valign="top" |
*Physical exam findings based on underlying components
| valign="top" |
*Elevated serum hCG, AFP, and/or PALP dependeing on the underlying compoenents 
| valign="top" |
*Imaging findings based on underlying components
| valign="top" |
*Histopathological findings based on underlying components
*Variable proportion of choriocarcinoma, embryonal cell carcinoma, yolk sac tumor, seminoma, and/or teratoma tissue
| valign="top" |
*May stain positively for any of CD30, hCG, AFP, ALP, c-KIT, CD30, EMA,  alpha-1-antitrypsin, PAS diastase, and glycogen depending on underlying compoenents
|-
| align="center" |
'''[[Carcinoid|Carcinoid<br>(pure neuroendocrine neoplasm)]]'''
| valign="top" |
*Middle-aged and elderly adult
*Manifests as a minimally painful, rapidly growing mass
*May manifest as carcinoid syndrome
| valign="top" |
*Tender testicular mass
*Hydrocele or cryptorchidism 
| valign="top" |
*Elevated serum and urine 5-HIAA if carcinoid syndrome present
| valign="top" |
*Unilateral, well-circumscribed mass without vascular invasion
*Solid and cystic appearance
*Mixed echogenicity on ultrasound
*Irregular calcifications 
| valign="top" |
*Well-circumscribed, yellowish solid mass
*Occasional cystic masses
*Small acini, cord-forming rosettes, prominent cytoplasmic granularity
*Salt and pepper chromatic pattern
*Absent features of atypia
*Neurosecretory granules on electron microscopy 
| valign="top" |
*Stains positively for cytokeratin, serotonin, chromogranin, synaptophysin, and CD56  
|-
| align="center" |
'''[[PNET|PNET<br>(Ewing's tumor of the testes)]]'''
| valign="top" |
*30-50 yo man with rapidly enlarging mass
*Often metastatic at presentation
| valign="top" |
*Palpable, nontender unilateral testicular mass 
| valign="top" |
*Unremarkable 
| valign="top" |
*No differentiating features on imaging
*Vascular flow on Doppler 
| valign="top" |
*Greyish necrotic mass of immature neural tissue
*Sheet-like / rosette distribution of small round blue tumor cells
*Neurosecretory granules on electron microscopy 
| valign="top" |
*Stains positively for synaptophysin, NSE, chromogranin, CD99, GFAP, FLI1
*Split of EWS gene on chromosome 22
|-
| colspan="7" style="background: #4479BA; width: 50px;" |{{fontcolor|#FFF|'''Sex-cord stromal tumors'''}}
|-
| align="center" |
'''[[Fibroma]]'''
| valign="top" |
*Middle-aged adult (range 20-70 years) with slowly-growing, painless testicular mass
*History of nevoid basal cell carcinoma (Gorlin syndrome) 
| valign="top" |
*Palpable, nontender unilateral testicular mass 
| valign="top" |
*Unremarkable 
| valign="top" |
*Isoechoic mass on ultrasound with prominent acoustic shadowing (fibrous component)
*May be homogeneous or heterogeneous
*Margins often blended with the tunica albuginea
*No vascular flow on Dopper 
| valign="top" |
*Well-circumscribed, often non-encapsulated solid pale yellow mass
*No hemorrhage, no necrosis
*Pure fibromatous features of collagenized plaques and spindle cells that synthesize collagen.
*Low cellularity 
| valign="top" |
*Mutation in ''PTCH'' gene
*Positive staining for calretinin, inhibin, CD56, CD34, actin, vimectin
*Usually (but not always) negative staining for S-100, keratin, CD99/MIC-2, and desmin 
|-
| align="center" |
'''[[Granulosa cell tumor]]'''
| valign="top" |
*Young or middle-aged adult (adult-type) or infant/child (juvenile-type) patient with slowly-enlarging painless testicular mass
*May manifest with symptoms of metastasis or hormonal secretion (e.g. gynecomastia in estrogen-secreting tumors) 
| valign="top" |
*Palpable, nontender unilateral testicular mass 
| valign="top" |
*Unremarkable 
| valign="top" |
*Hypoechoic mass with solid and cystic appearance on ultrasound (swiss-cheese appearance)
| valign="top" |
*Well-circumscribed tumor between the seminiferous tubules
*May be solid, cystic, of lobular
*Pseudo-capsule
*No hemorrhage, no necrosis
*Elongated grooved nuclei (coffee-bean appearance)
*Call-Exner bodies
*Variable atypia 
| valign="top" |
*Stains positively for calretinin, inhibin, vimentin, actin, and MIC2 
|-
| align="center" |
'''[[leydig cell tumor|Leydig (interstitial) cell tumor]]'''
| valign="top" |
*Bimodal age distribution
*Slowly enlarging painless unilateral mass 
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Signs of excess estradiol (e.g. gynecomastia)
| valign="top" |
*Unremarkable   
| valign="top" |
*Well-defined, hypoechoic solid mass on ultrasound
*May have cystic component
*Irregular calcifications 
| valign="top" |
*Well-circumscribed, unencapsulated solid mass
*Yellowish-brown tumor
*May have cystic, hemorrhagic, or necrotic areas
*Often dffuse growth of large polygonal Leydig cells, but may have unique patterns of growth
*Vacuolated cells with marked atypia
*Reinke crystals
*Psammoma bodies 
| valign="top" |
*Mutation in fumarate hydratase
*Stains positively for inhibin, cytokeratin, calretinin, synaptophysin, vimentin, Melan-A
|-
| align="center" |
'''[[sertoli cell|Sertoli hyperplasia<br>(Sertoli adenoma, Pick's adenoma)]]'''
| valign="top" |
*Child or young adult with history of Peutz-Jegher syndrome, androgen insensitivity syndrome, or McCune Albright syndrome
*Slowly enlarging painless bilateral masses 
| valign="top" |
*Palpable, nontender bilateral testicular masses
*Signs of excess estradiol (e.g. gynecomastia) 
| valign="top" |
*Elevated serum estradiol
*Elevated anti-Mullerian hormone and inhibin B
*Reduced androgen concentration 
| valign="top" |
*Hyperechogenic nodules on ultrasound 
| valign="top" |
*Well-demarcated yellowish nodules in the testis
*Unencapsulated nodules composed of Sertoli cells 
| valign="top" |
*Stains positively for anti-Mullerian hormone, inhibin A, CK8, and CK18
*Negative staining for AFP, hCG, and p53
|-
| align="center" |
'''[[sertoli cell|Large cell calcifying Sertoli cell tumor]]'''
| valign="top" |
*Young patient with history of Carney syndrome, Peutz-Jeghers syndrome, or tuberous sclerosis
*Slowly enlarging painless unilateral/bilateral mass(es)
| valign="top" |
*Palpable, nontender unilateral or bilateral testicular mass
*Signs of excess estradiol (e.g. gynecomastia) 
| valign="top" |
*Elevated serum estradiol 
| valign="top" |
*Diffuse and regular (smooth, rounded, large) calcifications
*Variable appearance on ultrasound
*Often multiple hyperechogenic regions with strong shadowing
*Possible increased blood flow 
| valign="top" |
*Multifocal, well-circumscribed yellowish-grey nodules
*Absent hemorrhage or necrosis
*Patterrns (sheet or trabeculae) of large cells and formation of solid tubules
*Psammoma bodies
*Charcot Bottcher crystals on electron microscopy  
| valign="top" |
*Stains positively for inhibin, vimentin, calretinin, S100, and cytokeratin
*Negative staining for laminin, PALP, AFP, and hCG
|-
| align="center" |
'''[[Sertoli-Leydig cell tumor|Sclerosing Sertoli cell tumor]]'''
| valign="top" |
*Variable age at presentation (adolescence to elderly)
*Slowly enlarging painless unilateral mass 
| valign="top" |
*Palpable, nontender unilateral testicular mass 
| valign="top" |
*Unremarkable 
| valign="top" |
*Well-circumscribed hypoechogenic lesion on ultrasound 
| valign="top" |
*Well-circumscribed, yellowish-grey nodule
*Absent hemorrhage or necrosis
*Tubuules and cords of Sertoli cells surrounded by hypocellular collagenous strome (sclerosis) 
| valign="top" |
*Stains positively for calretinin, inhibin, and vimentin
*Negative staining for cytokeratin, AFP, and hCG
|-
| align="center" |
'''[[Sertoli-Leydig cell tumor|Sertoli tumor, non-specific]]'''
| valign="top" |
*Bimodal age districution: either 40-50 year old man or infants with history of Carney syndrome or Peutz-Jegher syndrome
*Slowly enlarging testicular mass
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Signs of excess estradiol (e.g. gynecomastia) 
| valign="top" |
*Often unremarkable
*Elevated serum estradiol may be present, less common 
| valign="top" |
*Well-circumscribed mass with variable echogenicity 
| valign="top" |
*Well-circumscribed, yellowish-grey nodule
*Hemorrhage and necrosis may be present, but uncommon
*Features of fetal, prepubertal, and adult Sertoli cells present simultaneously
*Charcot Bottcher crystals on electron microscopy 
| valign="top" |
*Stains positively for vimentin, cytokeratin, inhibin, S100, chromogranin, synaptophysin, and CD99
*Negative staining for hCG, AFP, and PLAP 
|-
| align="center" |
'''[[Sertoli-Leydig cell tumor|Sertoli-Leylig cell tumor (SLCT)]]'''
| valign="top" |
*Young adult or phenotypic female with history of androgen insensitivity
*Slowly enlarging painless unilateral mass 
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Signs of excess estradiol (e.g. gynecomastia) 
| valign="top" |
*Often unremarkable
*Elevated serum estradiol may be present, less common
*Abrnomally elevated testosterone among pts with androgen insensitivity 
| valign="top" |
*Well-circumscribed mass with variable echogenicity
*Solid mass with intratumoral cysts may be present
| valign="top" |
*Heterogeneous, lobulated, encapsulated yellowish solid mass
*Mass contains combination of Sertoli cells and Leydig cells 
*Poorly differentiated cells (immature tubules of Sertoli cells, large Leydig cells) 
| valign="top" |
*Stains positively for inhibin, melanA, and CD99
*Negative staining for EMA, PLAP, and S100
|-
| align="center" |
'''[[CAH|Testicular tumor of andrenogenital syndrome<br>(testicular adrenal rest tumor)]]'''
| valign="top" |
*Post-pubertal patient with history of congenital adrenal hyperplasia (CAH)
*Often asymptomatic, detected during screening in patients with CAH 
| valign="top" |
*Unremarkable testicular exam
*Other signs of congenital adrenal hyperplasia 
| valign="top" |
*Elevated 11-beta-hydroxylase activity
*Reduced concentrations of AFP, LDH, and hCG 
| valign="top" |
*Uniform hypoechogenicity on ultrasound
*Usually multifocal and bilateral lesions 
| valign="top" |
*Hyperplasia, bilateral lesions in testicular hilum
*Yellowish nodules
*Cells resemble adrenocortical cells, no mitoses
*Normal surrounding tissue
*Absent Reinke crystals
| valign="top" |
*Stains positively for CD56, synaptophysin, and inhibin
*Negative staining for androgen receptor protein
|-
| colspan="7" style="background: #4479BA; width: 50px;" |{{fontcolor|#FFF|'''Other tumors'''}}
|-
| align="center" |
'''[[Lymphoma]]'''
| valign="top" |
*Elderly patient (>60 years) with history of lymphoma (commonly diffuse large B cell lymphoma)
*Unilateral or bilateral painless testicular mass 
| valign="top" |
*Palpable, nontender unilateral or bilateral testicular mass 
| valign="top" |
*Depends on lymphoma subtype 
| valign="top" |
*Diffuse infiltration
*Hypoechoic solid masses on ultrasound
*Hypervascularity on Doppler ultrasound 
| valign="top" |
*Whitish-tan colored mass
*Large, pleomorphic malignant cells
*Seminiferous tubules may be spared or undergo sclerosis
*Vascular invasion   
| valign="top" |
*Stains positively for CD45
*Depends mainly on lymphoma subtype
*Usually negative staining for PLAP and SALL4
|-
| align="center" |
'''[[Angiosarcoma]]'''
| valign="top" |
*Bimodal age distribution
*Young man with history of teratoma or elderly man with history of radiation or chronic hydrocele
*Painless/painful testicular mass 
| valign="top" |
*Tender or non-tender testicular mass
*Low-grade fever
*Scrotal swelling
*Flank pain
*Hydrocele 
| valign="top" |
*Often unremarkable 
| valign="top" |
*Hypervascularity on Doppler ultrasound 
| valign="top" |
*Solid vascular lesion
*Classical pattern of proliferating anastomosing blood-filled channels
*2 patterns: solid (sheet proliferation without lumen) and primitive (small lumina filled withblood)
| valign="top" |
*Stains positively for CD31, CD34, lectin, and factor VIII-related antigen
*Negative staining for pancytokeratin, PLAP, CD45, CD68, CAM5.2, and AE1/AE3 
|-
| align="center" |
'''[[Chondrosarcoma]]'''
| valign="top" |
*Young or middle-aged adult with history of teratoma
*Painless testicular mass 
| valign="top" |
*Palpable, non-tender, heterogeneous mass 
| valign="top" |
*Often unremarkable 
| valign="top" |
*Lobulated mass 
| valign="top" |
*Firm, grey mass with irregular lobulations
*Cartilaginous (chondroid) matrix surrounded by fibrovascular bands
*Most have non-cartilagenous components (rarely pure)
| valign="top" |
*Stains positively for S100
|-
| align="center" |
'''[[Hemangioma]]'''
| valign="top" |
*Painless testicular mass among pts of any age 
| valign="top" |
*Palpable, non-tender, homogeneous mass 
| valign="top" |
*Often unremarkable 
| valign="top" |
*Homogeneous hypoechoic mass
*Hypervascularity on Doppler ultrasound
| valign="top" |
*Well-defined hemorrhagic mass
*Red blood cells in tubules 
| valign="top" |
*Stains positively for CD31, CD34, FLI1, and factor VIII-related antigen
*Negative staining for pancytokeratin, AE, keratin, PLAP, and EMA
|-
| align="center" |
'''[[Mesothelioma]]'''
| valign="top" |
*Middle aged man with painless testicular mass and history of hydrocele or exposure to asbestos
| valign="top" |
*Palpable, non-tender testicular mass
*Scrotal swelling 
| valign="top" |
*Often unremarkable 
| valign="top" |
*Thickening of tunica vaginais
*Solid paratesticular mass
*Hydrocele 
| valign="top" |
*May be benign or malignant
*Papillary patterns of uniform epithelioid cells with fibrovacular core
*Polygonal cells with microvilli on electron microscopy
*Psammoma bodies 
| valign="top" |
*Benign: stains positively for p53 (focal) and CEA
*Malignant: Stains positively for calretinin, WT1, EMA, thrombomodulin, CK5, CK6, CK7 and negative staining for CEA and CK20  
|-
| align="center" |
'''[[Plasmacytoma]]'''
| valign="top" |
*Adult (of any age) with concurrent or history of plasma cell neoplasia (commonly multiple myeloma)
*Symptoms of multiple myeloma (e.g. fatigue, back pain) 
| valign="top" |
*Testicular exam unremarkable 
| valign="top" |
*Lab findings of plasmacytosis (e.g. anemia, elevated creatinine, hypercalcemia)
*No specific lab finding for testicular involvement 
| valign="top" |
*Poorly circumscribed hypoechoic lesions on ultrasound
*Hypervascularity on Doppler ultrasound 
| valign="top" |
*Large, tan-yellow mass
*Areas of hemorrahge
*Atypical plasma cells
*Tubule effacement in the center and tubule sparing in the periphery 
| valign="top" |
*Positive staining for EMA, CD45, CD79am CD138, kappa or lambda light chains, and other plasma cell markers
|-
| align="center" |
'''[[AIDS|AIDS-related testicular cancer]]'''
| valign="top" |
*Commonly testicular lymphoma or germ cell tumor
*Patient with history of AIDS presents with testicular swelling or pain
*Systemic manifestations of underlying malignancy 
| valign="top" |
*Palpable testicular mass that may be tender or non-tender 
| valign="top" |
*Depends on underlying malignancy
| valign="top" |
*Depends on underlying malignancy 
| valign="top" |
*Depends on underlying malignancy   
| valign="top" |
*Depends on underlying malignancy 
|-
| colspan="7" style="background: #4479BA; width: 50px;" |{{fontcolor|#FFF|'''Non-neoplastic mass'''}}
|-
| align="center" |
'''[[adrenal cortex|Adrenal cortical rest]]'''
| valign="top" |
*Usually asymptomatic (incidental finding)
*Young man with scrotal swelling and dull pain
*History of congenital adrenal hyperplasia (hydroxylase deficiency)
| valign="top" |
*Scrotal swelling 
| valign="top" |
*May be unremarkable
*If secretory, elevated concentration of adrenal hormone 
| valign="top" |
*Heterogeneous, well-circumscribed hypoechoic mass on ultrasound
*No or minimal vascularity on Doppler
*No distinguishing features 
| valign="top" |
*Well-circumscribed, small, round, orange-yellow nodule
*Adrenal cortical tissue with absence of adrenal medullary tissue 
| valign="top" |
*Positive staining for  markers of cortical adrenal tissue 
|-
| align="center" |
'''[[filariasis|Chylocele]]'''
| valign="top" |
*Scrotal swelling in a man with history of filariasis / elephantiasis 
| valign="top" |
*Scrotal swelling
*Negative trans-illumination test
| valign="top" |
*Unremarkable 
| valign="top" |
*Fluid collection surrounding the testes 
| valign="top" |
*Milky chylous fluid (not waterry) on aspiration
*Usually no evidence of microfliariae in chylous fluid
*Abundant leukocytes 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Congenital cystic dysplasia|Cystic dysplasia]]'''
| valign="top" |
*Young child with history of renal agenesis / dysplasia
*May be unilateral or bilateral, painless testicular mass 
| valign="top" |
*Palpable, non-tender testicular mass 
| valign="top" |
*Unremarkable 
| valign="top" |
*Irregular cystic spaces witht varying sizes
*Absence of solid or vascular components 
| valign="top" |
*Varying cystic spaces
*Formation of incomplete connective tissue septa
*Cells resembling the normal adult rete testes 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Dermoid cyst]]'''
| valign="top" |
*Young or middle aged adult with slowly growing painless mass
*Ruptured cyst may manifest with scrotal swelling, erythema, and pain 
| valign="top" |
*Palpable, nontender unilateral testicular mass
*Usually heterogeneous enlargement 
| valign="top" |
*Unremarkable 
| valign="top" |
*Onioin-skin appearance on ultrasound
*Target-shape lesions with halo of hypoechonicity and central hyperechogenicity on ultrasound
*No vacular flow on Doppler 
| valign="top" |
*Mature epithelial tissue
*May have hair (similar to teratoma)
*Keratin filled cyst
*Epidermal epithelium surrounded by pilosebaceious units
*Formation of lipogranulomas and microcalcifications
*Absence of atypia
| valign="top" |
*Absence of any mutation (normal 12p)
*Stains positively for cytokeratin


== Risk factors==
|-
Associated risk factors leading to female breast cancer<ref name="pmid25114845">{{cite journal| author=Shah R, Rosso K, Nathanson SD| title=Pathogenesis, prevention, diagnosis and treatment of breast cancer. | journal=World J Clin Oncol | year= 2014 | volume= 5 | issue= 3 | pages= 283-98 | pmid=25114845 | doi=10.5306/wjco.v5.i3.283 | pmc=4127601 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25114845 }} </ref>
| align="center" |
* Age: probability of breast cancer from birth to 39 years; 1 in 202, from 40 to 59 years; 1 in 26, from 60 to 69 years; 1 in 28.
'''[[Epidermoid cyst|Epidermoid cyst<br>(keratocyst)]]'''
*Personal history of breast cancer
| valign="top" |
*Breast pathology: PD with atypia has greater risk of developing to breast cancer in comparison of PD.
*10-40 yo
*Family history: greater breast cancer risk in women with first degree relatives with breast cancer under 50 years old.
*Painless slowly growing testicular mass
*Genetic predisposition
*Ruptured cyst may manifest with scrotal swelling, erythema, and pain
**High risk
| valign="top" |
*** BRCA1
*Palpable, non-tender testicular mass
***BRCA2
*Usually heterogeneous enlargement 
**Moderate risk
| valign="top" |
*** Homozygous ataxia-telangiectasia (ATM)
*Unremarkable 
*** Somatic mutation in CHEK2
| valign="top" |
***BRCA1 modifier gene: BRIP1
*Onioin-skin appearance on ultrasound
***BRCA2 modifier gene: PALB2
*Target-shape lesions with halo of hypoechonicity and central hyperechogenicity on ultrasound
** Low risk
*No vacular flow on Doppler 
***These alleles have not designated yet.
| valign="top" |
Endogenous hormone exposure and reproductive factors:
*Absence of dermal structures, such as hair, sebaceous glands etc. (found in dermoid cyst)
* Early menarche;under age of 13 years
*Cyst with white keratin debris
*Parity; nulliparous is associated with incresed risk of breast cancer
*Lined by squamous epithelium
*Age at first full term pregnancy; younger age may decrease risk of breast cancer
*Laminated keratin
*Breast feeding; decreased risk of breast cancer
*Granuloma when cyst ruptures 
* Testostrone; increased relative risk to 2.86-3.28
| valign="top" |
*Age at menopause;older menopausal age associated with greater risk of breast cancer
*Absence of any mutation (normal 12p) 
Exogenous hormone exposure
|-
*long term exposure> 5 years; increases chances of breast cancer
| align="center" |
*Time of usage;nearly menopausal age associated with development to breast cancer
'''[[orchitis|Granulomatous orchitis]]'''
Lifestyle
| valign="top" |
These factors may increase risk of developing breast cancers
*40-60 yo man with sudden-onset testicular tenderness and mass formation
* Alcohol consumption; even as 5.0 to 9.9 per day, approximately 3 to 6 drinks per week, developed with relative risk 1.15
*History of infection, sarcoidosis, or testicular trauma 
*Inactivity
| valign="top" |
*Obesity; BMI:25-29.9 and BMI>30 have relative risk about 1.28
*Tender testicular mass
*Previous history of radiation;at the age< 35years old
*Fever 
| valign="top" |
*Unremarkable 
| valign="top" |
*Solid hypoechoic mass 
| valign="top" |
*Solid nodule
*Lymphocytic infiltration and formation of giant cells and macrophages
*Not true granuloma 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Hematocele]]'''
| valign="top" |
*Scrotal mass in patients with history of testicular trauma, torsion, or increased bleeding tendency 
| valign="top" |
*Scrotal swelling
*Negative trans-illumination test
| valign="top" |  
*Unremarkable
| valign="top" |
*Fluid collection surrounding the testes 
| valign="top" |
*Bloody fluid on aspiration 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Hydrocele]]'''
| valign="top" |
*Scrotal mass in patients with history of testicular trauma or epidymitis
| valign="top" |
*Scrotal swelling
*'''Positive''' trans-illumination test
| valign="top" |
*Unremarkable 
| valign="top" |
*Fluid collection surrounding the testes 
| valign="top" |
*Clear fluid on aspiration 
| valign="top" |
*N/
|-
| align="center" |
'''[[Macroorchidism]]'''
| valign="top" |
*History of fragile X syndrome, FSH secreting adenoma 
| valign="top" |
*Large testicle (the testicle itself is large)
*Signs of underlying disease 
| valign="top" |
*May have elevated hormone concentration (e.g. FSH) if secretory adenoma 
| valign="top" |
*Large testicle, but normal architecture 
| valign="top" |
*Normal testicular findings 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Malakoplakia]]'''
| valign="top" |
*Young man with long-standing symptoms of orchi-epididymitis (pain, scrotal swelling)
*History of immunosuppression 
| valign="top" |
*Palpable, tender testicular mass
*Scrotal swelling
*Erythema 
| valign="top" |
*Positive culture results for bacterial infection (chronic inflammation) 
| valign="top" |
*Hypoechogenic mass on ultrasound
*Increased vascularity on Doppler 
| valign="top" |
*Soft yellow friable plaques (malakos=soft | plakos=plaques)
*Von Hansemann cells (large cells with abundant eosinophilic cytoplasm) and Michaelis-Gutmann bodies (intracytoplasmic inclusion bodies with owl eyes appearance)
| valign="top" |
*N/A
|-
| align="center" |
'''[[vasculitis|Testicular vasculitits]]'''
| valign="top" |
*Middle aged man with history of polyarteritis nodosa (less commonly granulomatosis with polyangiomatosis, Henoch-Schonlein purpura, or giant cell arteritis)
*History of HBV or HIV
Painful testicular mass with intra-testicular hemorrhage
*Symptoms of underlying vasculitis 
| valign="top" |
*Signs of underlying vasculitis
*Palpable, tender testicular mass
*Scrotal swelling if vasculitis includes extratesticular structures 
| valign="top" |
*Unremarkable 
| valign="top" |
*Heterogeneous, hypoechogenic lesion on ultrasound
*Inreased intralesional vascularity on Doppler 
| valign="top" |
*Soft, dark red lesion with areas of hemorrhage
*Fibrinoid necrosis
*Vascular wall fibrosis 
| valign="top" |
*N/
|-
| align="center" |
'''[[Fibrous connective tissue|Fibrous proliferation<br>(paratesticular fibrous pseudotumor)]]'''
| valign="top" |
*Patients of all ages (peak during young adulthood)
*Slowly growing painless unilateral scrotal masss
*History of genitourinary infection or trauma
| valign="top" |
*Palpable, non-tender scrotal mass 
| valign="top" |
*Unremarkable
| valign="top" |
*Paratesticular mass between tunica layers
*Hypoechogenic solid mass on ultrasound
*No vascularity on Doppler 
| valign="top" |
*Whitish mass with multinoduular thickening
*Collagen-rich fibrous tissue with increased fibroblasts
*Dystrophic calcifications
*No hemorrhage or necrosis 
| valign="top" |
*Stains positiively for actin and keratin
*Negative staining for ALK-1, beta-catenin
|-
| align="center" |
'''[[testis|Polyorchism<br>(supranumerary testes)]]'''
| valign="top" |
*Often asymptomatic (incidental finding)
*Young patient with scrotal pain, swelling, hydrocele, varicocele
*Patients may present with testicular torsion 
| valign="top" |
*Palpable, non-tender scrotal mass
*Scrotal swelling
*Testicular torsion manifests with excruciating testicular or pelvic pain, erythema, and swelling
| valign="top" |
*Unremarkable 
| valign="top" |
*Isoechogenic scrotal mass 
| valign="top" |
*Normal testicular tissue 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Spermatocele]]'''
| valign="top" |
*Young or middle aged adult with painless testicular or scrotal mass 
| valign="top" |
*Homogeneous palpable non-tender testicular or scrotal mass
| valign="top" |
*Unremarkable 
| valign="top" |
*Well-defined, homogeneous,, hypoechoic mass on ultrasound
*Increased vascular flow on Doppler 
| valign="top" |
*Splenic tissue (red with clear boundaries)
*Occasional calcification, thrombi, or fibrosis 
| valign="top" |
*N/A
|-
| align="center" |
'''[[spleen|Splenogodal fusion syndrome<br>(ectopic scrotal spleen)]]'''
| valign="top" |
*Child or adolescent with painless, left scrotal mass (not right) and history of perimelia (continuous subtype) or cardiac defect (discontinuous subtype) 
| valign="top" |
*Homogeneous palpable non-tender scrotal mass 
| valign="top" |
*Unremarkable
| valign="top" |
*Well-defined, homogeneous,, hypoechoic mass on ultrasound
*Increased vascular flow on Doppler 
| valign="top" |
*Splenic tissue (red with clear boundaries)
*Occasional calcification, thrombi, or fibrosis 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Varicocele]]'''
| valign="top" |
*Often asymptomatic
*Dull or sharp testicular pain that increases with standing or physical activity and improves when lying down
*History of infertility 
| valign="top" |
*Scrotal mass and swelling
*Often left-sided
*Dilated, tortuous veins
*"Bag of worms" sensation upon palpation  
| valign="top" |
*Unremarkable
| valign="top" |
*On ultrasound, CT/MRI, and venography, apperance of dilated pampiniform plexus veins with serpentine appearance is diagnostic
*Flow reversal (reflux) with Valsalva maneuver on Doppler
*Enhancement following administration of gadolinium on MRI 
| valign="top" |
*Testicular atrophy in advanced cases 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Testicular torsion]]'''
| valign="top" |
*Excruciating, acute, sharp testicular pain that radiates to the pelvis and abdomen
*Testicular swelling and pain 
| valign="top" |
*Scrotal swelling and tenderness 
| valign="top" |
*Unremarkable 
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*No blood flow on Doppler (vs. increased flow in infections)
*Scrotal wall thickening 
| align="center" | --- 
| valign="top" |
*N/A 
|-
| colspan="7" style="background: #4479BA; width: 50px;" |{{fontcolor|#FFF|'''Scrotal'''}}
|-
| align="center" |
'''[[Brucellosis]]'''
| valign="top" |
*Patient with history of exposure to cattle/sheep/goat/swine or animal products (milk, meat, cheese) presents with acute scrotal pain and swelling
*Undulant fever and night sweats (characteristic wet hay odor)
*Relapses common with similar symptoms 
| valign="top" |
*Tender testicular mass
*Fever
*Hydrocele 
| valign="top" |
*Elevated WBC count
*Positive serum STA test for brucellosis
*Elevated Brucella IgM and IgG antibodies
*Urine PCR positive for Brucella 
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*Focal/diffusre increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Granulomatous inflammation with lymphocytic infiltration 
| valign="top" |
*Urethral Gram stain demonstrates Gram-negative diplococci
|-
| align="center" |
'''[[Brucellosis]]'''
| valign="top" |
*Patient with history of exposure to cattle/sheep/goat/swine or animal products (milk, meat, cheese) presents with acute scrotal pain and swelling
Undulant fever and night sweats (characteristic wet hay odor)
*Relapses common with similar symptoms 
| valign="top" |
*Tender testicular mass
*Fever
*Hydrocele 
| valign="top" |
*Elevated WBC count
*Positive serum STA test for brucellosis
*Elevated Brucella IgM and IgG antibodies
*Urine PCR positive for Brucella spp.
| valign="top" |
*Focal/diffuse heterogeneous, hypoechoic intratesticular mass on ultrasound
*Focal/diffuse increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Abscess formation at diagnosis is common
*Grey-white mass suggestive of testicular atrophy
*Granulomatous inflammation with lymphocytic infiltration 
| valign="top" |
*N/A
|-
| align="center" |
'''[[Gonorrhea|Gonorrhea infection]]'''
| valign="top" |
*Patient with history of unprotected sexual intercourse presents with unilaterla testicular pain, swelling, and fever
*May be either acute or chronic 
| valign="top" |
*Tender testicular mass
*Fever
*Hydrocele
| valign="top" |
*Elevated WBC count
*Gram-negative diplococci on urethral Gram stain
*Urine PCR positive for Gonorrhea 
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*Focal/diffusre increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Granulomatous inflammation with lymphocytic infiltration 
| valign="top" |
*Urethral Gram stain demonstrates Gram-negative diplococci
|-
| align="center" |
'''[[Histoplasmosis|Histoplasma infection]]'''
| valign="top" |
*Chronic testicular enlargement
*Patients may have systemic manifestations of histoplasmosis
| valign="top" |
*Tender/non-tender testicular mass 
| valign="top" |
*Elevated WBC count and eosinophilia may be present (may be normal in chronic cases)  
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*Focal/diffusre increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Caseating granuloma with giant cells 
| valign="top" |
*Yeast observed on silver stain
|-
| align="center" |
'''[[Mumps]]'''
| valign="top" |
*Post-pubertal man with recent manifestations of mumps (e.g. parotiditis, pancreatitis, arthritis, myocarditis, meningoencephalitis) presents with acute, unilateral painful testicular mass 
| valign="top" |
*Tender testicular mass
*Hydrocele
*Fever
*Parotiditis
*Rash 
| valign="top" |
*Elevated WBC
*Elevated paramyxovirus IgM and IgG
*Urine PCR positive for paramyxovirus 
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*Focal/diffusre increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Non-specific interstitial edema, degenerative changes, vascular dilation
*Lymphocytic infiltration
| valign="top" |
*N/A 
|-
| align="center" |
'''[[epididymo-orchitis|Pyogenic epididymo-orchitis]]'''
| valign="top" |
*Patient with history of unprotected sexual intercourse presents with acute scrotal swelling and pain 
| valign="top" |
*Tender testicular mass
*Fever
*Hydrocele 
| valign="top" |
*Elevated WBC
*Bacterial growth on urethral swab specimin (usually E. coli)
*Urine PCR positive for offending bacterial agent
| valign="top" |
*Focal/diffuse hypoechogenicity on ultrasound
*Focal/diffusre increased blood flow on Doppler
*Scrotal wall thickening 
| valign="top" |
*Abscess formation in advanced cases
*Non-specific interstitial edema, degenerative changes, vascular dilation
*Lymphocytic infiltration
*Grey-white mass suggestive of testicular atrophy
| valign="top" |
*N/A
|-
| align="center" |
'''[[Syphilis]]'''
| valign="top" |
*Patient with long history of unprotected sexual intercourse presents with painful testicular swelling (tertiary syphilis)
*Often manifests as epidimo-orchitis that is resistant to conventional antibiotic therapy
*May have other systemic symptoms of tertiary syphilis 
| valign="top" |
*Irregular tender testicular mass
*Thickened epididymis
*Hydrocele 
| valign="top" |
*Positive syphilis serology (suggest latent syphilis)
*VDRL may be either positiive or negative
*Positive dark field microscopy from lesion content 
| valign="top" |
*Heterogeneous hypoechogenicity on ultrasound
*Solid and cystic appearance with areas of necrosis
*May have increased blood flow on Doppler 
| valign="top" |
*Discrete gummas on gross pathology
*Microscopic features of gumma (interstitial inflammation, lymphocytic and plasma cell infiltration, obliterative endorteritis (endoarteritis obliterans), perivascular cuffing)
*Spirochetes may occasionally be observed 
| valign="top" |
*May stain positively for silver-based methods (Warthin-Starry stain, Wright stain, Levaditi stain) 
|-
| align="center" |
'''[[Tuberculosis]]'''
| valign="top" |
*Patient with history of tuberculosis presents with painless mass or chronically dull testicular discomfort
*Positive constitutional symptoms (weight loss, malaise)
*May be isolated or may be associated with other systemic symptoms of tuberculosis (e.g. lymphadenopathy, pulmonary lesions, renal involvement)
*May have concomitant involvement of other GU organs (e.g. prostate, seminal vesicles) 
| valign="top" |
*Irregular testicular mass
*May be tender or non-tender
*Thickened scrotal skin
*Hydrocele
| valign="top" |
*Ejaculum may demonstrate positive acid fast bacilli (AFB) staining 
| valign="top" |
*Heterogeneous hypoechogenicity on ultrasound
*No/minimal blood flow on Doppler
*Hypointense lesion on T1WI MRI and hyperintense on T2WI MRI
| valign="top" |
*Possible abscess formation
*Caseating necrosis
*Epithelioid cells and lymphocytic infiltration with presence of multinucleated giant cells
| valign="top" |
|}


==Screening==
The Screening methods of breast lesions<ref name="pmid25114845">{{cite journal| author=Shah R, Rosso K, Nathanson SD| title=Pathogenesis, prevention, diagnosis and treatment of breast cancer. | journal=World J Clin Oncol | year= 2014 | volume= 5 | issue= 3 | pages= 283-98 | pmid=25114845 | doi=10.5306/wjco.v5.i3.283 | pmc=4127601 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25114845  }} </ref>:
* Breast examination
** Self breast examination
*** Although this is controversial, most clinicians recommend women to perform self examination monthly
**Clinical breast examination
*** Women with age> 40 years is recommended for clinical breast examination annually
*Ultrasound
** whole breast ultrasound detects lesions in dense breast tissue which could not be diagnosed by mammography <ref name="pmid19727744">{{cite journal| author=Kelly KM, Dean J, Comulada WS, Lee SJ| title=Breast cancer detection using automated whole breast ultrasound and mammography in radiographically dense breasts. | journal=Eur Radiol | year= 2010 | volume= 20 | issue= 3 | pages= 734-42 | pmid=19727744 | doi=10.1007/s00330-009-1588-y | pmc=2822222 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19727744  }} </ref>
*Mammography
**Gold standard of screening
**Early detection of non-palpabale masses
**Regarding to 2013 NCCN guidelines annual screening in average risk women aged≥ 40 years
**Regarding to 2013 NCCN guidelines annual screening in high risk women from age of 25 years
**Sensitivity of 0.33-0.39 and specificity of 0.95
*Magnetic resonance imaging (MRI)
**Significant method for detection, assessment and management of breast cancer
**Sensitivity of 0.77-0.79 and specificity of 0.86-0.89
** Based on 2013 NCCN guidelines annual MRI for individuals with > 20% risk of developing breast cancer in lifetime starting at age of 25 years
** Beneficial modality in high risk individuals
** Valuable in individuals with equivocal results from other screening tests
**Usable for individuals with ineffective mammography results due to breast augmentation


==History and symptoms==
'''History'''
By clinical history, the cancer risk can be evaluated <ref name="pmid25114845">{{cite journal| author=Shah R, Rosso K, Nathanson SD| title=Pathogenesis, prevention, diagnosis and treatment of breast cancer. | journal=World J Clin Oncol | year= 2014 | volume= 5 | issue= 3 | pages= 283-98 | pmid=25114845 | doi=10.5306/wjco.v5.i3.283 | pmc=4127601 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25114845  }} </ref>
*Age at menarche
*Menopausal status
*number of pregnancies
*Previous history of radiation
*History of oral contraceptives or hormone replacement therapy
*Past history of breast cancer and age at time of diagnosis
*Familial history of breast cancer or ovarian cancer in first-degree relatives
*Other associated breast disease or possible biopsies
'''Symptoms'''
* Breast Pain
**Cyclic pain
*** Occurring at the late luteal phase of menstural cycle, relieving at the onset of menstural phase
**Non- cyclic pain
***[[Fat necrosis]] from trauma
***stretching [[cooper's ligament]]
***[[Mastitis]]( focal or periductal)
***Cyst
***[[Mondors's disease]]
***[[Hidradenitis supporativa]]
**Non-breast pain
***Chest-wall pain
**** [[Tietz syndrome]]
***Non chest-wall pain
****[[Gall bladder disease]]
****[[Ischemic heart disease]]
*Nipple discharge
**Presence of galactorrhea
***[[Hyperprolactinemia]] from pituitary tumor
***[[Hyperthyroidism]]
***Drugs
**Absence of galactorrhea
***Fron one duct
**** Intraductal papilloma
****[[Ductal carcinoma in situ]]
****[[Paget's disease]]
***From multiple ducts
****[[Fibrocyctic changes]]
****[[Ductal ectasia]]
*Malaise
*Body pain
*Weight loss
{{Family tree/start|||||||||||||||||||||||||||A0= breast lumps symtoms||||||||||||||||||||||||||}}
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==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Latest revision as of 19:23, 22 January 2019


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shadan Mehraban, M.D.[2]

Overview

Disease Name History and Symptoms Physical Examination Lab Findings Imaging Findings Gross and Histologic Findings Genetic Studies / Immunohistochemistry
Germ Cell Tumors

Seminoma

  • Most common
  • 30-50 year-old with painless unilateral testicular mass or mild discomfort
  • Palpable, nontender unilateral testicular mass
  • Usually homogeneous enlargement
  • Elevated serum placental ALP (PALP)
  • Hypoechogenic intratesticular well-defined mass on ultrasound with internal blood flow on Doppler ultrasound
  • Cysts and calcificications are uncommon
  • Hypointense lesion with inhomogeneous enhancement on MRI
  • Homogeneous when small and heterogeneous when large
  • Grey-white homogeneous mass with a lobular appearance
  • Fried egg appearance on histopathology (large cells and clear cytoplasm)
  • Prominent lymphocytic infiltration and less commonly, granulomatous formation
  • Stains positively for ALP, c-KIT, CD30, EMA, and glycogen

Embryonal cell carcinoma

  • Young adults
  • Painful testicular mass
  • Manifests with early mestastasis (bone, lung, CNS)
  • Often unremarkable (small primary tumor)
  • Elevated serum hCG
  • Elevated serum AFP, when mixed
  • Variable echogenicity (usually hypoechoic on ultrasound)
  • No differentiating features on imaging
  • Commonly invade the surrounding structures (tunica albuginea)
  • Irregular calcifications
  • Pale-grey mass with areas of hemorrhagic and necrosis
  • Often mixed histopathological features (solid, papillary, tubular, pseudoglandular)
  • Stains positively for CD30 and hCG stain
  • May stain positively for AFP, when mixed

Yolk sac tumor

  • Most common testicular cancer in children less than 3 years of age
  • Rapidly growing unilateral mass in an infant or a young child
  • Palpable, nontender unilateral testicular mass
  • Usually heterogeneous enlargement
  • Elevated serum AFP
  • Diffuse enlargement of the testis with a heterogeneous appearance on ultrasound
  • Areas of hemorrhage and necrosis on MRI
  • Yellow, mucinous, non-encapsulated, heterogeneous mass with areas of necrosis and hemorrhage
  • Patterns that resemble embryonal structures (yolk sac, allantois) with reticular, papillary, or elongated forms
  • Schiller-Duval bodies (perivascular structures)
  • Stains positively for AFP, alpha-1-antitrypsin, PAS diastase

Teratoma

  • Bimodal distribution of age (infants and middle aged adults)
  • Painless tumor
  • History of congenital disease (Down syndrome, klinefelter, spina bifida)
  • Palpable, nontender unilateral testicular mass
  • Usually heterogeneous enlargement
  • Elevated serum hCG
  • Elevated serum AFP
  • Heterogeneous, cystic appearance with mucinous or sebaceous depositions
  • Variable echogenicity on ultrasound
  • Calcifications usually irregular
  • Large, heterogeneous appearance with solid, cystic, mucoid, and/or cartilageanous components
  • Presence of at least 2 germ layers
  • Chromosome 12p mutations
  • Stains positively for cytokeratin. hCG, and AFP

Teratocarcinoma

  • Middle aged adult with painless testicular mass of mild discomfort
  • May manifest with features of metastasis
  • Palpable, nontender unilateral testicular mass
  • Usually heterogeneous enlargement
  • Elevated serum hCG
  • Elevated serum AFP
  • Variable echogenicity on ultrasound
  • Features of both teratoma and embryonal carcinoma (more common) or both teratoma and choriocarcinoma (less common)
  • Solid and cystic components with mucoid, cartilagenous, sebaceous gland, myxoid stroma components
  • Additional features of underlying embryonal carcinoma or choriocarcinoma
  • Stains positively for cytokeratin. hCG, AFP, and CD30

Choriocarcinoma

  • Adolescent or young adult with extratesticular symptoms
  • Mass is small and locally asymptomatic
  • Manifests with early metastasis and signs of hemorrhage (hemorrhagic stroke, hyperthyroidism, cannon-ball metastasis in lung, liver involvement, neurological deficits)
  • Often unremarkable (small primary tumor)
  • Elevated serum hCG
  • Variable echogenicity
  • No differentiating features on imaging
  • Commonly invade the surrounding structures (tunica albuginea)
  • Prominent areas of hemorrhage and necrosis
  • Nest and sheet pattern that simultaneously includes both cytotrophoblast and syncytiotrophoblast (rarely pure)
  • Paucity of intermediate trophoblasts (unlike placental site trophoblastic tumor)
  • Stains positively for hCG

Diffuse embryoma

  • 20-25 yo man with painful testicular mass
  • Tender testicular mass
  • Elevated serum hCG
  • Elevated serum AFP
  • Poorly-defined, heterogeneous hyperechoic mass on ultrasound
  • Non-encapsulated mass
  • Intermingled (lace-like) embryonal carcinoma and yolk sac components in equal proportions, but no discrete embyoid bodies
  • Scattered trophoblastic components
  • Necklace-like arrangement of cells
  • Stains positively for cytokeratin, AFP (yolk sac component), and CD30 (embyonal component)

Polyembryoma

  • 20-25 yo man with painful testicular mass
  • Tender testicular mass
  • Elevated serum AFP
  • Elevated serum hCG
  • Poorly-defined, heterogeneous hyperechoic mass on ultrasound
  • Multiple discrete embyoid bodies (combination of both embryonal carcinoma and yolk sac components)
  • Stains positively for cytokeratin, AFP (yolk sac component), and CD30 (embyonal component)

Placental site trophoblastic tumor

  • Infant or young adult
  • Painful small testicular mass
  • Small nontender or minimally painful testicular mass
  • Elevated serum hCG
  • Variable echogenicity
  • No differentiating features on imaging
  • May have vascular flow
  • Solid yellowish mass that resembles uterine tissue
  • Less prominent foci of hemorrhage and ncerosis
  • Predominance of intermediate trophoblast cells (implantation-site type) that invade surrounding blood vessels
  • Paucity of cytotrophoblast and syncytiotrophoblast cells (unlike choriocarcinoma)
  • Stains positively for hPL (diffuse), cytokeratin, AFP, and hCG (patchy)
  • Negative p63 staining

Epithelioid trophoblastic tumor

  • Infant or young adult
  • Painful small testicular mass
  • Small nontender or minimally painful testicular mass
  • Elevated serum hCG
  • Variable echogenicity
  • No differentiating features on imaging
  • May have vascular flow
  • Solid yellowish mass that resembles uterine tissue
  • Less prominent foci of hemorrhage and ncerosis
  • Predominance of intermediate trophoblast cells (implantation-site type) that invade surrounding blood vessels
  • Paucity of cytotrophoblast and syncytiotrophoblast cells (unlike choriocarcinoma)
  • Stains positively for p63 (diffuse), p63, cytokeratin, AFP, and hCG (patchy)
  • Negative hPL staining

Mixed germ cell tumor

  • Typical age at diagnosis and other clinical features based on underlying components
  • Physical exam findings based on underlying components
  • Elevated serum hCG, AFP, and/or PALP dependeing on the underlying compoenents
  • Imaging findings based on underlying components
  • Histopathological findings based on underlying components
  • Variable proportion of choriocarcinoma, embryonal cell carcinoma, yolk sac tumor, seminoma, and/or teratoma tissue
  • May stain positively for any of CD30, hCG, AFP, ALP, c-KIT, CD30, EMA, alpha-1-antitrypsin, PAS diastase, and glycogen depending on underlying compoenents

Carcinoid
(pure neuroendocrine neoplasm)

  • Middle-aged and elderly adult
  • Manifests as a minimally painful, rapidly growing mass
  • May manifest as carcinoid syndrome
  • Tender testicular mass
  • Hydrocele or cryptorchidism
  • Elevated serum and urine 5-HIAA if carcinoid syndrome present
  • Unilateral, well-circumscribed mass without vascular invasion
  • Solid and cystic appearance
  • Mixed echogenicity on ultrasound
  • Irregular calcifications
  • Well-circumscribed, yellowish solid mass
  • Occasional cystic masses
  • Small acini, cord-forming rosettes, prominent cytoplasmic granularity
  • Salt and pepper chromatic pattern
  • Absent features of atypia
  • Neurosecretory granules on electron microscopy
  • Stains positively for cytokeratin, serotonin, chromogranin, synaptophysin, and CD56

PNET
(Ewing's tumor of the testes)

  • 30-50 yo man with rapidly enlarging mass
  • Often metastatic at presentation
  • Palpable, nontender unilateral testicular mass
  • Unremarkable
  • No differentiating features on imaging
  • Vascular flow on Doppler
  • Greyish necrotic mass of immature neural tissue
  • Sheet-like / rosette distribution of small round blue tumor cells
  • Neurosecretory granules on electron microscopy
  • Stains positively for synaptophysin, NSE, chromogranin, CD99, GFAP, FLI1
  • Split of EWS gene on chromosome 22
Sex-cord stromal tumors

Fibroma

  • Middle-aged adult (range 20-70 years) with slowly-growing, painless testicular mass
  • History of nevoid basal cell carcinoma (Gorlin syndrome)
  • Palpable, nontender unilateral testicular mass
  • Unremarkable
  • Isoechoic mass on ultrasound with prominent acoustic shadowing (fibrous component)
  • May be homogeneous or heterogeneous
  • Margins often blended with the tunica albuginea
  • No vascular flow on Dopper
  • Well-circumscribed, often non-encapsulated solid pale yellow mass
  • No hemorrhage, no necrosis
  • Pure fibromatous features of collagenized plaques and spindle cells that synthesize collagen.
  • Low cellularity
  • Mutation in PTCH gene
  • Positive staining for calretinin, inhibin, CD56, CD34, actin, vimectin
  • Usually (but not always) negative staining for S-100, keratin, CD99/MIC-2, and desmin

Granulosa cell tumor

  • Young or middle-aged adult (adult-type) or infant/child (juvenile-type) patient with slowly-enlarging painless testicular mass
  • May manifest with symptoms of metastasis or hormonal secretion (e.g. gynecomastia in estrogen-secreting tumors)
  • Palpable, nontender unilateral testicular mass
  • Unremarkable
  • Hypoechoic mass with solid and cystic appearance on ultrasound (swiss-cheese appearance)
  • Well-circumscribed tumor between the seminiferous tubules
  • May be solid, cystic, of lobular
  • Pseudo-capsule
  • No hemorrhage, no necrosis
  • Elongated grooved nuclei (coffee-bean appearance)
  • Call-Exner bodies
  • Variable atypia
  • Stains positively for calretinin, inhibin, vimentin, actin, and MIC2

Leydig (interstitial) cell tumor

  • Bimodal age distribution
  • Slowly enlarging painless unilateral mass
  • Palpable, nontender unilateral testicular mass
  • Signs of excess estradiol (e.g. gynecomastia)
  • Unremarkable
  • Well-defined, hypoechoic solid mass on ultrasound
  • May have cystic component
  • Irregular calcifications
  • Well-circumscribed, unencapsulated solid mass
  • Yellowish-brown tumor
  • May have cystic, hemorrhagic, or necrotic areas
  • Often dffuse growth of large polygonal Leydig cells, but may have unique patterns of growth
  • Vacuolated cells with marked atypia
  • Reinke crystals
  • Psammoma bodies
  • Mutation in fumarate hydratase
  • Stains positively for inhibin, cytokeratin, calretinin, synaptophysin, vimentin, Melan-A

Sertoli hyperplasia
(Sertoli adenoma, Pick's adenoma)

  • Child or young adult with history of Peutz-Jegher syndrome, androgen insensitivity syndrome, or McCune Albright syndrome
  • Slowly enlarging painless bilateral masses
  • Palpable, nontender bilateral testicular masses
  • Signs of excess estradiol (e.g. gynecomastia)
  • Elevated serum estradiol
  • Elevated anti-Mullerian hormone and inhibin B
  • Reduced androgen concentration
  • Hyperechogenic nodules on ultrasound
  • Well-demarcated yellowish nodules in the testis
  • Unencapsulated nodules composed of Sertoli cells
  • Stains positively for anti-Mullerian hormone, inhibin A, CK8, and CK18
  • Negative staining for AFP, hCG, and p53

Large cell calcifying Sertoli cell tumor

  • Young patient with history of Carney syndrome, Peutz-Jeghers syndrome, or tuberous sclerosis
  • Slowly enlarging painless unilateral/bilateral mass(es)
  • Palpable, nontender unilateral or bilateral testicular mass
  • Signs of excess estradiol (e.g. gynecomastia)
  • Elevated serum estradiol
  • Diffuse and regular (smooth, rounded, large) calcifications
  • Variable appearance on ultrasound
  • Often multiple hyperechogenic regions with strong shadowing
  • Possible increased blood flow
  • Multifocal, well-circumscribed yellowish-grey nodules
  • Absent hemorrhage or necrosis
  • Patterrns (sheet or trabeculae) of large cells and formation of solid tubules
  • Psammoma bodies
  • Charcot Bottcher crystals on electron microscopy
  • Stains positively for inhibin, vimentin, calretinin, S100, and cytokeratin
  • Negative staining for laminin, PALP, AFP, and hCG

Sclerosing Sertoli cell tumor

  • Variable age at presentation (adolescence to elderly)
  • Slowly enlarging painless unilateral mass
  • Palpable, nontender unilateral testicular mass
  • Unremarkable
  • Well-circumscribed hypoechogenic lesion on ultrasound
  • Well-circumscribed, yellowish-grey nodule
  • Absent hemorrhage or necrosis
  • Tubuules and cords of Sertoli cells surrounded by hypocellular collagenous strome (sclerosis)
  • Stains positively for calretinin, inhibin, and vimentin
  • Negative staining for cytokeratin, AFP, and hCG

Sertoli tumor, non-specific

  • Bimodal age districution: either 40-50 year old man or infants with history of Carney syndrome or Peutz-Jegher syndrome
  • Slowly enlarging testicular mass
  • Palpable, nontender unilateral testicular mass
  • Signs of excess estradiol (e.g. gynecomastia)
  • Often unremarkable
  • Elevated serum estradiol may be present, less common
  • Well-circumscribed mass with variable echogenicity
  • Well-circumscribed, yellowish-grey nodule
  • Hemorrhage and necrosis may be present, but uncommon
  • Features of fetal, prepubertal, and adult Sertoli cells present simultaneously
  • Charcot Bottcher crystals on electron microscopy
  • Stains positively for vimentin, cytokeratin, inhibin, S100, chromogranin, synaptophysin, and CD99
  • Negative staining for hCG, AFP, and PLAP

Sertoli-Leylig cell tumor (SLCT)

  • Young adult or phenotypic female with history of androgen insensitivity
  • Slowly enlarging painless unilateral mass
  • Palpable, nontender unilateral testicular mass
  • Signs of excess estradiol (e.g. gynecomastia)
  • Often unremarkable
  • Elevated serum estradiol may be present, less common
  • Abrnomally elevated testosterone among pts with androgen insensitivity
  • Well-circumscribed mass with variable echogenicity
  • Solid mass with intratumoral cysts may be present
  • Heterogeneous, lobulated, encapsulated yellowish solid mass
  • Mass contains combination of Sertoli cells and Leydig cells
  • Poorly differentiated cells (immature tubules of Sertoli cells, large Leydig cells)
  • Stains positively for inhibin, melanA, and CD99
  • Negative staining for EMA, PLAP, and S100

Testicular tumor of andrenogenital syndrome
(testicular adrenal rest tumor)

  • Post-pubertal patient with history of congenital adrenal hyperplasia (CAH)
  • Often asymptomatic, detected during screening in patients with CAH
  • Unremarkable testicular exam
  • Other signs of congenital adrenal hyperplasia
  • Elevated 11-beta-hydroxylase activity
  • Reduced concentrations of AFP, LDH, and hCG
  • Uniform hypoechogenicity on ultrasound
  • Usually multifocal and bilateral lesions
  • Hyperplasia, bilateral lesions in testicular hilum
  • Yellowish nodules
  • Cells resemble adrenocortical cells, no mitoses
  • Normal surrounding tissue
  • Absent Reinke crystals
  • Stains positively for CD56, synaptophysin, and inhibin
  • Negative staining for androgen receptor protein
Other tumors

Lymphoma

  • Elderly patient (>60 years) with history of lymphoma (commonly diffuse large B cell lymphoma)
  • Unilateral or bilateral painless testicular mass
  • Palpable, nontender unilateral or bilateral testicular mass
  • Depends on lymphoma subtype
  • Diffuse infiltration
  • Hypoechoic solid masses on ultrasound
  • Hypervascularity on Doppler ultrasound
  • Whitish-tan colored mass
  • Large, pleomorphic malignant cells
  • Seminiferous tubules may be spared or undergo sclerosis
  • Vascular invasion
  • Stains positively for CD45
  • Depends mainly on lymphoma subtype
  • Usually negative staining for PLAP and SALL4

Angiosarcoma

  • Bimodal age distribution
  • Young man with history of teratoma or elderly man with history of radiation or chronic hydrocele
  • Painless/painful testicular mass
  • Tender or non-tender testicular mass
  • Low-grade fever
  • Scrotal swelling
  • Flank pain
  • Hydrocele
  • Often unremarkable
  • Hypervascularity on Doppler ultrasound
  • Solid vascular lesion
  • Classical pattern of proliferating anastomosing blood-filled channels
  • 2 patterns: solid (sheet proliferation without lumen) and primitive (small lumina filled withblood)
  • Stains positively for CD31, CD34, lectin, and factor VIII-related antigen
  • Negative staining for pancytokeratin, PLAP, CD45, CD68, CAM5.2, and AE1/AE3

Chondrosarcoma

  • Young or middle-aged adult with history of teratoma
  • Painless testicular mass
  • Palpable, non-tender, heterogeneous mass
  • Often unremarkable
  • Lobulated mass
  • Firm, grey mass with irregular lobulations
  • Cartilaginous (chondroid) matrix surrounded by fibrovascular bands
  • Most have non-cartilagenous components (rarely pure)
  • Stains positively for S100

Hemangioma

  • Painless testicular mass among pts of any age
  • Palpable, non-tender, homogeneous mass
  • Often unremarkable
  • Homogeneous hypoechoic mass
  • Hypervascularity on Doppler ultrasound
  • Well-defined hemorrhagic mass
  • Red blood cells in tubules
  • Stains positively for CD31, CD34, FLI1, and factor VIII-related antigen
  • Negative staining for pancytokeratin, AE, keratin, PLAP, and EMA

Mesothelioma

  • Middle aged man with painless testicular mass and history of hydrocele or exposure to asbestos
  • Palpable, non-tender testicular mass
  • Scrotal swelling
  • Often unremarkable
  • Thickening of tunica vaginais
  • Solid paratesticular mass
  • Hydrocele
  • May be benign or malignant
  • Papillary patterns of uniform epithelioid cells with fibrovacular core
  • Polygonal cells with microvilli on electron microscopy
  • Psammoma bodies
  • Benign: stains positively for p53 (focal) and CEA
  • Malignant: Stains positively for calretinin, WT1, EMA, thrombomodulin, CK5, CK6, CK7 and negative staining for CEA and CK20

Plasmacytoma

  • Adult (of any age) with concurrent or history of plasma cell neoplasia (commonly multiple myeloma)
  • Symptoms of multiple myeloma (e.g. fatigue, back pain)
  • Testicular exam unremarkable
  • Lab findings of plasmacytosis (e.g. anemia, elevated creatinine, hypercalcemia)
  • No specific lab finding for testicular involvement
  • Poorly circumscribed hypoechoic lesions on ultrasound
  • Hypervascularity on Doppler ultrasound
  • Large, tan-yellow mass
  • Areas of hemorrahge
  • Atypical plasma cells
  • Tubule effacement in the center and tubule sparing in the periphery
  • Positive staining for EMA, CD45, CD79am CD138, kappa or lambda light chains, and other plasma cell markers

AIDS-related testicular cancer

  • Commonly testicular lymphoma or germ cell tumor
  • Patient with history of AIDS presents with testicular swelling or pain
  • Systemic manifestations of underlying malignancy
  • Palpable testicular mass that may be tender or non-tender
  • Depends on underlying malignancy
  • Depends on underlying malignancy
  • Depends on underlying malignancy
  • Depends on underlying malignancy
Non-neoplastic mass

Adrenal cortical rest

  • Usually asymptomatic (incidental finding)
  • Young man with scrotal swelling and dull pain
  • History of congenital adrenal hyperplasia (hydroxylase deficiency)
  • Scrotal swelling
  • May be unremarkable
  • If secretory, elevated concentration of adrenal hormone
  • Heterogeneous, well-circumscribed hypoechoic mass on ultrasound
  • No or minimal vascularity on Doppler
  • No distinguishing features
  • Well-circumscribed, small, round, orange-yellow nodule
  • Adrenal cortical tissue with absence of adrenal medullary tissue
  • Positive staining for markers of cortical adrenal tissue

Chylocele

  • Scrotal swelling in a man with history of filariasis / elephantiasis
  • Scrotal swelling
  • Negative trans-illumination test
  • Unremarkable
  • Fluid collection surrounding the testes
  • Milky chylous fluid (not waterry) on aspiration
  • Usually no evidence of microfliariae in chylous fluid
  • Abundant leukocytes
  • N/A

Cystic dysplasia

  • Young child with history of renal agenesis / dysplasia
  • May be unilateral or bilateral, painless testicular mass
  • Palpable, non-tender testicular mass
  • Unremarkable
  • Irregular cystic spaces witht varying sizes
  • Absence of solid or vascular components
  • Varying cystic spaces
  • Formation of incomplete connective tissue septa
  • Cells resembling the normal adult rete testes
  • N/A

Dermoid cyst

  • Young or middle aged adult with slowly growing painless mass
  • Ruptured cyst may manifest with scrotal swelling, erythema, and pain
  • Palpable, nontender unilateral testicular mass
  • Usually heterogeneous enlargement
  • Unremarkable
  • Onioin-skin appearance on ultrasound
  • Target-shape lesions with halo of hypoechonicity and central hyperechogenicity on ultrasound
  • No vacular flow on Doppler
  • Mature epithelial tissue
  • May have hair (similar to teratoma)
  • Keratin filled cyst
  • Epidermal epithelium surrounded by pilosebaceious units
  • Formation of lipogranulomas and microcalcifications
  • Absence of atypia
  • Absence of any mutation (normal 12p)
  • Stains positively for cytokeratin

Epidermoid cyst
(keratocyst)

  • 10-40 yo
  • Painless slowly growing testicular mass
  • Ruptured cyst may manifest with scrotal swelling, erythema, and pain
  • Palpable, non-tender testicular mass
  • Usually heterogeneous enlargement
  • Unremarkable
  • Onioin-skin appearance on ultrasound
  • Target-shape lesions with halo of hypoechonicity and central hyperechogenicity on ultrasound
  • No vacular flow on Doppler
  • Absence of dermal structures, such as hair, sebaceous glands etc. (found in dermoid cyst)
  • Cyst with white keratin debris
  • Lined by squamous epithelium
  • Laminated keratin
  • Granuloma when cyst ruptures
  • Absence of any mutation (normal 12p)

Granulomatous orchitis

  • 40-60 yo man with sudden-onset testicular tenderness and mass formation
  • History of infection, sarcoidosis, or testicular trauma
  • Tender testicular mass
  • Fever
  • Unremarkable
  • Solid hypoechoic mass
  • Solid nodule
  • Lymphocytic infiltration and formation of giant cells and macrophages
  • Not true granuloma
  • N/A

Hematocele

  • Scrotal mass in patients with history of testicular trauma, torsion, or increased bleeding tendency
  • Scrotal swelling
  • Negative trans-illumination test
  • Unremarkable
  • Fluid collection surrounding the testes
  • Bloody fluid on aspiration
  • N/A

Hydrocele

  • Scrotal mass in patients with history of testicular trauma or epidymitis
  • Scrotal swelling
  • Positive trans-illumination test
  • Unremarkable
  • Fluid collection surrounding the testes
  • Clear fluid on aspiration
  • N/A

Macroorchidism

  • History of fragile X syndrome, FSH secreting adenoma
  • Large testicle (the testicle itself is large)
  • Signs of underlying disease
  • May have elevated hormone concentration (e.g. FSH) if secretory adenoma
  • Large testicle, but normal architecture
  • Normal testicular findings
  • N/A

Malakoplakia

  • Young man with long-standing symptoms of orchi-epididymitis (pain, scrotal swelling)
  • History of immunosuppression
  • Palpable, tender testicular mass
  • Scrotal swelling
  • Erythema
  • Positive culture results for bacterial infection (chronic inflammation)
  • Hypoechogenic mass on ultrasound
  • Increased vascularity on Doppler
  • Soft yellow friable plaques (malakos=soft | plakos=plaques)
  • Von Hansemann cells (large cells with abundant eosinophilic cytoplasm) and Michaelis-Gutmann bodies (intracytoplasmic inclusion bodies with owl eyes appearance)
  • N/A

Testicular vasculitits

  • Middle aged man with history of polyarteritis nodosa (less commonly granulomatosis with polyangiomatosis, Henoch-Schonlein purpura, or giant cell arteritis)
  • History of HBV or HIV

Painful testicular mass with intra-testicular hemorrhage

  • Symptoms of underlying vasculitis
  • Signs of underlying vasculitis
  • Palpable, tender testicular mass
  • Scrotal swelling if vasculitis includes extratesticular structures
  • Unremarkable
  • Heterogeneous, hypoechogenic lesion on ultrasound
  • Inreased intralesional vascularity on Doppler
  • Soft, dark red lesion with areas of hemorrhage
  • Fibrinoid necrosis
  • Vascular wall fibrosis
  • N/A

Fibrous proliferation
(paratesticular fibrous pseudotumor)

  • Patients of all ages (peak during young adulthood)
  • Slowly growing painless unilateral scrotal masss
  • History of genitourinary infection or trauma
  • Palpable, non-tender scrotal mass
  • Unremarkable
  • Paratesticular mass between tunica layers
  • Hypoechogenic solid mass on ultrasound
  • No vascularity on Doppler
  • Whitish mass with multinoduular thickening
  • Collagen-rich fibrous tissue with increased fibroblasts
  • Dystrophic calcifications
  • No hemorrhage or necrosis
  • Stains positiively for actin and keratin
  • Negative staining for ALK-1, beta-catenin

Polyorchism
(supranumerary testes)

  • Often asymptomatic (incidental finding)
  • Young patient with scrotal pain, swelling, hydrocele, varicocele
  • Patients may present with testicular torsion
  • Palpable, non-tender scrotal mass
  • Scrotal swelling
  • Testicular torsion manifests with excruciating testicular or pelvic pain, erythema, and swelling
  • Unremarkable
  • Isoechogenic scrotal mass
  • Normal testicular tissue
  • N/A

Spermatocele

  • Young or middle aged adult with painless testicular or scrotal mass
  • Homogeneous palpable non-tender testicular or scrotal mass
  • Unremarkable
  • Well-defined, homogeneous,, hypoechoic mass on ultrasound
  • Increased vascular flow on Doppler
  • Splenic tissue (red with clear boundaries)
  • Occasional calcification, thrombi, or fibrosis
  • N/A

Splenogodal fusion syndrome
(ectopic scrotal spleen)

  • Child or adolescent with painless, left scrotal mass (not right) and history of perimelia (continuous subtype) or cardiac defect (discontinuous subtype)
  • Homogeneous palpable non-tender scrotal mass
  • Unremarkable
  • Well-defined, homogeneous,, hypoechoic mass on ultrasound
  • Increased vascular flow on Doppler
  • Splenic tissue (red with clear boundaries)
  • Occasional calcification, thrombi, or fibrosis
  • N/A

Varicocele

  • Often asymptomatic
  • Dull or sharp testicular pain that increases with standing or physical activity and improves when lying down
  • History of infertility
  • Scrotal mass and swelling
  • Often left-sided
  • Dilated, tortuous veins
  • "Bag of worms" sensation upon palpation
  • Unremarkable
  • On ultrasound, CT/MRI, and venography, apperance of dilated pampiniform plexus veins with serpentine appearance is diagnostic
  • Flow reversal (reflux) with Valsalva maneuver on Doppler
  • Enhancement following administration of gadolinium on MRI
  • Testicular atrophy in advanced cases
  • N/A

Testicular torsion

  • Excruciating, acute, sharp testicular pain that radiates to the pelvis and abdomen
  • Testicular swelling and pain
  • Scrotal swelling and tenderness
  • Unremarkable
  • Focal/diffuse hypoechogenicity on ultrasound
  • No blood flow on Doppler (vs. increased flow in infections)
  • Scrotal wall thickening
---
  • N/A
Scrotal

Brucellosis

  • Patient with history of exposure to cattle/sheep/goat/swine or animal products (milk, meat, cheese) presents with acute scrotal pain and swelling
  • Undulant fever and night sweats (characteristic wet hay odor)
  • Relapses common with similar symptoms
  • Tender testicular mass
  • Fever
  • Hydrocele
  • Elevated WBC count
  • Positive serum STA test for brucellosis
  • Elevated Brucella IgM and IgG antibodies
  • Urine PCR positive for Brucella
  • Focal/diffuse hypoechogenicity on ultrasound
  • Focal/diffusre increased blood flow on Doppler
  • Scrotal wall thickening
  • Granulomatous inflammation with lymphocytic infiltration
  • Urethral Gram stain demonstrates Gram-negative diplococci

Brucellosis

  • Patient with history of exposure to cattle/sheep/goat/swine or animal products (milk, meat, cheese) presents with acute scrotal pain and swelling

Undulant fever and night sweats (characteristic wet hay odor)

  • Relapses common with similar symptoms
  • Tender testicular mass
  • Fever
  • Hydrocele
  • Elevated WBC count
  • Positive serum STA test for brucellosis
  • Elevated Brucella IgM and IgG antibodies
  • Urine PCR positive for Brucella spp.
  • Focal/diffuse heterogeneous, hypoechoic intratesticular mass on ultrasound
  • Focal/diffuse increased blood flow on Doppler
  • Scrotal wall thickening
  • Abscess formation at diagnosis is common
  • Grey-white mass suggestive of testicular atrophy
  • Granulomatous inflammation with lymphocytic infiltration
  • N/A

Gonorrhea infection

  • Patient with history of unprotected sexual intercourse presents with unilaterla testicular pain, swelling, and fever
  • May be either acute or chronic
  • Tender testicular mass
  • Fever
  • Hydrocele
  • Elevated WBC count
  • Gram-negative diplococci on urethral Gram stain
  • Urine PCR positive for Gonorrhea
  • Focal/diffuse hypoechogenicity on ultrasound
  • Focal/diffusre increased blood flow on Doppler
  • Scrotal wall thickening
  • Granulomatous inflammation with lymphocytic infiltration
  • Urethral Gram stain demonstrates Gram-negative diplococci

Histoplasma infection

  • Chronic testicular enlargement
  • Patients may have systemic manifestations of histoplasmosis
  • Tender/non-tender testicular mass
  • Elevated WBC count and eosinophilia may be present (may be normal in chronic cases)
  • Focal/diffuse hypoechogenicity on ultrasound
  • Focal/diffusre increased blood flow on Doppler
  • Scrotal wall thickening
  • Caseating granuloma with giant cells
  • Yeast observed on silver stain

Mumps

  • Post-pubertal man with recent manifestations of mumps (e.g. parotiditis, pancreatitis, arthritis, myocarditis, meningoencephalitis) presents with acute, unilateral painful testicular mass
  • Tender testicular mass
  • Hydrocele
  • Fever
  • Parotiditis
  • Rash
  • Elevated WBC
  • Elevated paramyxovirus IgM and IgG
  • Urine PCR positive for paramyxovirus
  • Focal/diffuse hypoechogenicity on ultrasound
  • Focal/diffusre increased blood flow on Doppler
  • Scrotal wall thickening
  • Non-specific interstitial edema, degenerative changes, vascular dilation
  • Lymphocytic infiltration
  • N/A

Pyogenic epididymo-orchitis

  • Patient with history of unprotected sexual intercourse presents with acute scrotal swelling and pain
  • Tender testicular mass
  • Fever
  • Hydrocele
  • Elevated WBC
  • Bacterial growth on urethral swab specimin (usually E. coli)
  • Urine PCR positive for offending bacterial agent
  • Focal/diffuse hypoechogenicity on ultrasound
  • Focal/diffusre increased blood flow on Doppler
  • Scrotal wall thickening
  • Abscess formation in advanced cases
  • Non-specific interstitial edema, degenerative changes, vascular dilation
  • Lymphocytic infiltration
  • Grey-white mass suggestive of testicular atrophy
  • N/A

Syphilis

  • Patient with long history of unprotected sexual intercourse presents with painful testicular swelling (tertiary syphilis)
  • Often manifests as epidimo-orchitis that is resistant to conventional antibiotic therapy
  • May have other systemic symptoms of tertiary syphilis
  • Irregular tender testicular mass
  • Thickened epididymis
  • Hydrocele
  • Positive syphilis serology (suggest latent syphilis)
  • VDRL may be either positiive or negative
  • Positive dark field microscopy from lesion content
  • Heterogeneous hypoechogenicity on ultrasound
  • Solid and cystic appearance with areas of necrosis
  • May have increased blood flow on Doppler
  • Discrete gummas on gross pathology
  • Microscopic features of gumma (interstitial inflammation, lymphocytic and plasma cell infiltration, obliterative endorteritis (endoarteritis obliterans), perivascular cuffing)
  • Spirochetes may occasionally be observed
  • May stain positively for silver-based methods (Warthin-Starry stain, Wright stain, Levaditi stain)

Tuberculosis

  • Patient with history of tuberculosis presents with painless mass or chronically dull testicular discomfort
  • Positive constitutional symptoms (weight loss, malaise)
  • May be isolated or may be associated with other systemic symptoms of tuberculosis (e.g. lymphadenopathy, pulmonary lesions, renal involvement)
  • May have concomitant involvement of other GU organs (e.g. prostate, seminal vesicles)
  • Irregular testicular mass
  • May be tender or non-tender
  • Thickened scrotal skin
  • Hydrocele
  • Ejaculum may demonstrate positive acid fast bacilli (AFB) staining
  • Heterogeneous hypoechogenicity on ultrasound
  • No/minimal blood flow on Doppler
  • Hypointense lesion on T1WI MRI and hyperintense on T2WI MRI
  • Possible abscess formation
  • Caseating necrosis
  • Epithelioid cells and lymphocytic infiltration with presence of multinucleated giant cells


References