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(Created page with " ==Differential Diagnosis== {{ddx0|Hodgkin's lymphoma}} {{ddx1|Sarcoidosis}} {{ddx1|Lymphocytic lymphoma}} {{ddx1|Miliary tuberculosis}} {{ddx1|Infectious mononucleosis}} {{dd...")
 
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{{ddx|Hodgkin's lymphoma}}
=====Clinical manifestations=====
* mental nerve neuropathy
* alcohol intolerance
* dermatitis, exfoliative
* epitrochlear lymph node enlargement
* inguinal lymph node enlargement
* hepatomegaly
* liver mass
* superior vena cava obstruction
* inferior vena cava obstruction
* femoral lymph node enlargement
* popliteal lymph node enlargement
* Pemberton sign positive
* fever, Pel-Ebstein
* ascites, chylous
* axillary lymph node enlargement
* erythema multiforme
* erythema nodosum
* hepatosplenomegaly
* mesenteric lymph node enlargement
* paraplegia
* pruritus
* spinal cord compression
* spleen enlargement
* urinary tract obstruction
* generalized diffuse lymph node enlargement
* airway compression or obstruction
* cryptococcosis
* bone pain
* cervical lymph node enlargement
* fever, recurrent
* recurrent infection
* lymph node, fixed
* neck mass
* night sweats
* anergy
* supraclavicular lymph node enlargement
* sweating increase
* fever unknown origin
* fever, remittent
* painless lymphadenopathy
* regional lymph node enlargement
=====Laboratory abnormalities=====
* nucleated red cells
* hypogammaglobulinemia
* pancytopenia
* lymphocytes decreased
* granulomas on biopsy
=====Radiographic features=====
* retroperitoneal lymph node enlargement
* abdominal ultrasound, biliary tract dilatation
* bone lesion
* chest xray mediastinal mass, adenopathy, or widening
* chest xray mediastinal mass middle
* mediastinal lymph node enlargement
* Anterior mediastinal mass on chest radiograph
* gallium scan, increased uptake, abdomen
* ivory vertebra
* gallium scan increased uptake, mediastinum
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{{ddx|Sarcoidosis}}
=====Clinical manifestations=====
=====Laboratory abnormalities=====
=====Radiographic features=====




Evidence of "HODGKINS DISEASE"  (COMMON)   
The following clinical manifestations (if present) would support this disease:
mental nerve neuropathy
alcohol intolerance
dermatitis, exfoliative
epitrochlear lymph node enlargement
inguinal lymph node enlargement
hepatomegaly
liver mass
superior vena cava obstruction
inferior vena cava obstruction
femoral lymph node enlargement
popliteal lymph node enlargement
Pemberton sign positive
fever, Pel-Ebstein
ascites, chylous
axillary lymph node enlargement
erythema multiforme
erythema nodosum
hepatosplenomegaly
mesenteric lymph node enlargement
paraplegia
pruritus
spinal cord compression
spleen enlargement
urinary tract obstruction
generalized diffuse lymph node enlargement
airway compression or obstruction
cryptococcosis
bone pain
cervical lymph node enlargement
fever, recurrent
recurrent infection
lymph node, fixed
neck mass
night sweats
anergy
supraclavicular lymph node enlargement
sweating increase
fever unknown origin
fever, remittent
painless lymphadenopathy
regional lymph node enlargement
The following lab data (if present) would be useful in establishing the presence of the disease:
nucleated red cells
retroperitoneal lymph node enlargement
hypogammaglobulinemia
pancytopenia
lymphocytes decreased
abdominal ultrasound, biliary tract dilatation
granulomas on biopsy
bone lesion
chest xray mediastinal mass, adenopathy, or widening
chest xray mediastinal mass middle
mediastinal lymph node enlargement
chest xray mediastinal mass anterior
bone marrow granulomas
gallium scan, increased uptake, abdomen
ivory vertebra
gallium scan increased uptake, mediastinum


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
corneal deposit  
* corneal deposit  
corneal opacity  
* corneal opacity  
parotid gland swelling  
* parotid gland swelling  
polyneuropathy  
* polyneuropathy  
cranial nerve paralysis  
* cranial nerve paralysis  
airway compression or obstruction  
* airway compression or obstruction  
retinal granuloma  
* retinal granuloma  
erythema nodosum  
* erythema nodosum  
uveitis  
* uveitis  
ankle pain  
* ankle pain  
facial paralysis  
* facial paralysis  
salivary gland swelling  
* salivary gland swelling  
splenomegaly, massive  
* splenomegaly, massive  
cryptococcosis  
* cryptococcosis  
generalized rash, papules (elevated, <0.5cm)  
* generalized rash, papules (elevated, <0.5cm)  
iridocyclitis  
* iridocyclitis  
iritis  
* iritis  
cough, dry  
* cough, dry  
night sweats  
* night sweats  
spleen enlargement  
* spleen enlargement  
uveitis, bilateral  
* uveitis, bilateral  
generalized diffuse lymph node enlargement  
* generalized diffuse lymph node enlargement  
polyarthritis  
* polyarthritis  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
heart conduction abnormality, electrocardiographic  
* heart conduction abnormality, electrocardiographic  
atrioventricular block  
* atrioventricular block  
hypercalcemia  
* hypercalcemia  
retroperitoneal lymph node enlargement  
* retroperitoneal lymph node enlargement  
pleural effusion, lymphocytes increased  
* pleural effusion, lymphocytes increased  
CXR lung cyst  
* CXR lung cyst  
lymphocytes decreased  
* lymphocytes decreased  
chest xray interstitial infiltrate ( incl. reticulonodular )  
* chest xray interstitial infiltrate ( incl. reticulonodular )  
hypercalciuria  
* hypercalciuria  
alkaline phosphatase, mild-moderate elevation  
* alkaline phosphatase, mild-moderate elevation  
gallium scan increased uptake, mediastinum  
* gallium scan increased uptake, mediastinum  
gallium scan increased uptake, lungs  
* gallium scan increased uptake, lungs  
PFT's: restrictive defect  
* PFT's: restrictive defect  
PFT's: diffusion capacity decreased  
* PFT's: diffusion capacity decreased  
mediastinal lymph node enlargement  
* mediastinal lymph node enlargement  
bone marrow granulomas  
* bone marrow granulomas  
serum angiotensin-converting enzyme elevated  
* serum angiotensin-converting enzyme elevated  
vitamin D, 1,25-dihydroxy, increased  
* vitamin D, 1,25-dihydroxy, increased  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
granulomas on biopsy  
* granulomas on biopsy  
chest xray hilar lymph node enlargement  
* chest xray hilar lymph node enlargement  


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
mental nerve neuropathy  
* mental nerve neuropathy  
dermatitis, exfoliative  
* dermatitis, exfoliative  
extremity paralysis, lower  
* extremity paralysis, lower  
gout  
* gout  
esophageal candidiasis  
* esophageal candidiasis  
abdominal mass  
* abdominal mass  
biliary tract obstruction  
* biliary tract obstruction  
breast mass  
* breast mass  
epitrochlear lymph node enlargement  
* epitrochlear lymph node enlargement  
erythema multiforme  
* erythema multiforme  
erythema nodosum  
* erythema nodosum  
esophageal obstruction  
* esophageal obstruction  
facial edema  
* facial edema  
gastric obstruction  
* gastric obstruction  
thyroid nodule  
* thyroid nodule  
hepatosplenomegaly  
* hepatosplenomegaly  
intestinal obstruction  
* intestinal obstruction  
intussusception  
* intussusception  
liver mass  
* liver mass  
mesenteric lymph node enlargement  
* mesenteric lymph node enlargement  
mucous membrane bleeding  
* mucous membrane bleeding  
night sweats  
* night sweats  
paraplegia  
* paraplegia  
pruritus  
* pruritus  
anergy  
* anergy  
spinal cord compression  
* spinal cord compression  
stool clay color  
* stool clay color  
stool color yellow  
* stool color yellow  
superior vena cava obstruction  
* superior vena cava obstruction  
supraclavicular lymph node enlargement  
* supraclavicular lymph node enlargement  
testicular mass  
* testicular mass  
urinary tract obstruction  
* urinary tract obstruction  
inferior vena cava obstruction  
* inferior vena cava obstruction  
generalized diffuse lymph node enlargement  
* generalized diffuse lymph node enlargement  
splenomegaly, massive  
* splenomegaly, massive  
femoral lymph node enlargement  
* femoral lymph node enlargement  
popliteal lymph node enlargement  
* popliteal lymph node enlargement  
airway compression or obstruction  
* airway compression or obstruction  
cryptococcosis  
* cryptococcosis  
recurrent infection  
* recurrent infection  
lymph node, fixed  
* lymph node, fixed  
neck mass  
* neck mass  
spleen enlargement  
* spleen enlargement  
fever unknown origin  
* fever unknown origin  
regional lymph node enlargement  
* regional lymph node enlargement  
painless lymphadenopathy  
* painless lymphadenopathy  
cancer  
* cancer  
lymphoma  
* lymphoma  
non-Hodgkin lymphoma  
* non-Hodgkin lymphoma  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
IVP bladder mass or abnormal shape  
* IVP bladder mass or abnormal shape  
hypercalcemia, extreme (>14 mg/dl)  
* hypercalcemia, extreme (>14 mg/dl)  
bone destruction  
* bone destruction  
kidney mass  
* kidney mass  
mediastinal lymph node enlargement  
* mediastinal lymph node enlargement  
prolonged bleeding time  
* prolonged bleeding time  
ESR markedly increased  
* ESR markedly increased  
retroperitoneal lymph node enlargement  
* retroperitoneal lymph node enlargement  
hypogammaglobulinemia  
* hypogammaglobulinemia  
bone lesion  
* bone lesion  
pancytopenia  
* pancytopenia  
lymphocytes decreased  
* lymphocytes decreased  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
chest xray mediastinal mass anterior  
* chest xray mediastinal mass anterior  
pleural effusion, exudate  
* pleural effusion, exudate  
bone marrow plasma cells increased  
* bone marrow plasma cells increased  
cryoglobulinemia  
* cryoglobulinemia  
abdominal ultrasound, biliary tract dilatation  
* abdominal ultrasound, biliary tract dilatation  
pleural effusion, lymphocytes increased  
* pleural effusion, lymphocytes increased  
pleural effusion, chylous  
* pleural effusion, chylous  
malignant ascites  
* malignant ascites  
gallium scan increased uptake, mediastinum  
* gallium scan increased uptake, mediastinum  
gallium scan, increased uptake, abdomen  
* gallium scan, increased uptake, abdomen  
vitamin D, 1,25-dihydroxy, increased  
* vitamin D, 1,25-dihydroxy, increased  


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
prison inmate  
* prison inmate  
retinal granuloma  
* retinal granuloma  
erythema nodosum  
* erythema nodosum  
Haiti  
* Haiti  
immunosuppressive therapy  
* immunosuppressive therapy  
weight loss, severe  
* weight loss, severe  
corticosteroid use  
* corticosteroid use  
chest pain, pleuritic  
* chest pain, pleuritic  
dyspnea, progressive  
* dyspnea, progressive  
fever unknown origin  
* fever unknown origin  
retinitis  
* retinitis  
tuberculosis exposure  
* tuberculosis exposure  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
pancytopenia  
* pancytopenia  
PPD positive  
* PPD positive  
nucleated red cells  
* nucleated red cells  
gallium scan, increased uptake, abdomen  
* gallium scan, increased uptake, abdomen  
abdominal CT: multiple hypodense liver lesions  
* abdominal CT: multiple hypodense liver lesions  
bone marrow granulomas  
* bone marrow granulomas  
AFB smear positive  
* AFB smear positive  
chest xray multiple pulmonary nodules, non-calcified  
* chest xray multiple pulmonary nodules, non-calcified  
granulomas on biopsy  
* granulomas on biopsy  


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:


optic neuritis  
* optic neuritis  
epitrochlear lymph node enlargement  
* epitrochlear lymph node enlargement  
periorbital edema  
* periorbital edema  
pharyngeal petechia  
* pharyngeal petechia  
spleen enlargement  
* spleen enlargement  
spleen palpable  
* spleen palpable  
tonsillitis  
* tonsillitis  
abdominal tenderness, left upper quadrant  
* abdominal tenderness, left upper quadrant  
axillary lymph node enlargement  
* axillary lymph node enlargement  
inguinal lymph node enlargement  
* inguinal lymph node enlargement  
mesenteric lymph node enlargement  
* mesenteric lymph node enlargement  
pharyngeal exudate  
* pharyngeal exudate  
pharyngeal erythema  
* pharyngeal erythema  
spleen tenderness  
* spleen tenderness  
tonsillar exudate  
* tonsillar exudate  
generalized diffuse lymph node enlargement  
* generalized diffuse lymph node enlargement  
cervical lymph node enlargement  
* cervical lymph node enlargement  
pharyngeal swelling  
* pharyngeal swelling  
sore throat  
* sore throat  


The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:


SGPT (ALT), marked elevation  
* SGPT (ALT), marked elevation  
SGPT (ALT), elevated  
* SGPT (ALT), elevated  
lymphocytes increased  
* lymphocytes increased  
atypical lymphocytes increased  
* atypical lymphocytes increased  
heterophile antibody positive  
* heterophile antibody positive  
monocytes, increased  
* monocytes, increased  
Epstein-Barr virus titre positive
* Epstein-Barr virus titre positive




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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
cocaine use  
* cocaine use  
Turner syndrome  
* Turner syndrome  
Pemberton sign positive  
* Pemberton sign positive  
marfan syndrome  
* marfan syndrome  
aortic valve regurgitation  
* aortic valve regurgitation  
superior vena cava obstruction  
* superior vena cava obstruction  
aortic dilation, ascending  
* aortic dilation, ascending  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
chest xray mediastinal mass middle  
* chest xray mediastinal mass middle  
chest xray mediastinal mass posterior  
* chest xray mediastinal mass posterior  
mediastinal widening  
* mediastinal widening  
chest xray aorta prominent or enlarged  
* chest xray aorta prominent or enlarged  
chest xray mediastinal mass anterior  
* chest xray mediastinal mass anterior  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  




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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
upper extremity edema  
* upper extremity edema  
chest mass  
* chest mass  
neck mass  
* neck mass  
thyroid enlargement  
* thyroid enlargement  
tracheal compression  
* tracheal compression  
Pemberton sign positive  
* Pemberton sign positive  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
TSH elevated  
* TSH elevated  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
chest xray mediastinal mass anterior  
* chest xray mediastinal mass anterior  
 


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Evidence of "THYMOMA"  (RARE)     
Evidence of "THYMOMA"  (RARE)     
   
   
The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
bulbar palsy  
* bulbar palsy  
facial candida infection  
* facial candida infection  
facial cyanosis  
* facial cyanosis  
jugular venous distention  
* jugular venous distention  
mouth candida infection  
* mouth candida infection  
superior vena cava obstruction  
* superior vena cava obstruction  
diplopia  
* diplopia  
Pemberton sign positive  
* Pemberton sign positive  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
pancytopenia  
* pancytopenia  
antistriational antibodies  
* antistriational antibodies  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
chest xray mediastinal mass anterior  
* chest xray mediastinal mass anterior  




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Evidence of "ACTINOMYCOSIS"  (RARE)
Evidence of "ACTINOMYCOSIS"  (RARE)
The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
 
* tongue mass  
tongue mass  
* trismus  
trismus  
* pericardial constriction  
pericardial constriction  
* pharyngeal swelling  
pharyngeal swelling  
* pharyngeal tenderness  
pharyngeal tenderness  
* abdominal fistula  
abdominal fistula  
* bronchial fistula  
bronchial fistula  
* empyema  
empyema  
* lung abscess  
lung abscess  
* abdominal mass, right lower quadrant  
abdominal mass, right lower quadrant  
* chest wall suppuration  
chest wall suppuration  
* gingival fistula  
gingival fistula  
* chest wall fistula  
chest wall fistula  
* gingival swelling  
gingival swelling  
* gingival tenderness  
gingival tenderness  
* jaw induration  
jaw induration  
* mandibular swelling  
mandibular swelling  


The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
 
* echocardiogram: intracardiac mass  
echocardiogram: intracardiac mass  
* hepatic cyst(s)  
hepatic cyst(s)  
* mediastinal lymph node enlargement  
mediastinal lymph node enlargement  
* chest xray mediastinal mass, adenopathy, or widening  
chest xray mediastinal mass, adenopathy, or widening  
* Gram stain: branching Gram-positive bacilli  
Gram stain: branching Gram-positive bacilli  
* sulfur granule
sulfur granule


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
skin infiltration  
* skin infiltration  
sternal tenderness  
* sternal tenderness  
lymph node firmness  
* lymph node firmness  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
hemolysis  
* hemolysis  
mediastinal lymph node enlargement  
* mediastinal lymph node enlargement  
prolonged bleeding time  
* prolonged bleeding time  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
monoclonal gammopathy  
* monoclonal gammopathy  
cryoglobulinemia  
* cryoglobulinemia  
leukocytes, marked increase  
* leukocytes, marked increase  
flow cytometry: clonal B-lymphocytes  
* flow cytometry: clonal B-lymphocytes  
lymphocytes increased  
* lymphocytes increased  
   
   
The following findings (if present) would make this disease less likely:
The following findings (if present) would make this disease less likely:
left shift  
* left shift  
metamyelocytes increased  
* metamyelocytes increased  
 


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:


stridor  
* stridor  
facial erythema  
* facial erythema  
forehead vein distention  
* forehead vein distention  
lymphoma  
* lymphoma  
tracheal displacement  
* tracheal displacement  
chest vein distention  
* chest vein distention  
facial cyanosis  
* facial cyanosis  
collateral circulation increase  
* collateral circulation increase  
conjunctival edema  
* conjunctival edema  
conjunctival vein distention  
* conjunctival vein distention  
upper extremity edema  
* upper extremity edema  
upper extremity erythema  
* upper extremity erythema  
head edema  
* head edema  
jugular venous distention with inspiration  
* jugular venous distention with inspiration  
lung tumor  
* lung tumor  
extremity cyanosis  
* extremity cyanosis  
upper extremity vein distention  
* upper extremity vein distention  
facial edema  
* facial edema  
neck edema  
* neck edema  
jugular venous distention  
* jugular venous distention  
lung cancer  
* lung cancer  
upper extremity cyanosis  
* upper extremity cyanosis  
facial vein distention  
* facial vein distention  
superior vena cava obstruction  
* superior vena cava obstruction  


The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:


mediastinal lymph node enlargement  
* mediastinal lymph node enlargement  
chest xray pulmonary nodule (< 4 cm), non-calcified  
* chest xray pulmonary nodule (< 4 cm), non-calcified  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  


The following findings (if present) would exclude this disease:
The following findings (if present) would exclude this disease:


hepatojugular reflux
* hepatojugular reflux


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Evidence of "UNICENTRIC CASTLEMAN DISEASE"  (RARE)     
Evidence of "UNICENTRIC CASTLEMAN DISEASE"  (RARE)     
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
* The following lab data (if present) would be useful in establishing the presence of the disease:
mediastinal lymph node enlargement  
* mediastinal lymph node enlargement  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
 
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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
ankylosis  
* ankylosis  
hepatosplenomegaly  
* hepatosplenomegaly  
weight loss, severe  
* weight loss, severe  
fever, recurrent  
* fever, recurrent  
night sweats  
* night sweats  
wrist pain  
* wrist pain  
generalized diffuse lymph node enlargement  
* generalized diffuse lymph node enlargement  
fever unknown origin  
* fever unknown origin  
fever, remittent  
* fever, remittent  
fever, high grade  
* fever, high grade  
polyarticular  
* polyarticular  
rash, evanescent  
* rash, evanescent  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
leukocytes, marked increase  
* leukocytes, marked increase  
ESR markedly increased  
* ESR markedly increased  
serum ferritin greatly increased  
* serum ferritin greatly increased  
   
   
The following findings (if present) would make this disease less likely:
The following findings (if present) would make this disease less likely:
monoarticular  
* monoarticular  
   
   
The following findings (if present) would exclude this disease:
The following findings (if present) would exclude this disease:
asymptomatic  
* asymptomatic  


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
acanthosis nigricans  
* acanthosis nigricans  
axillary lymph node enlargement  
* axillary lymph node enlargement  
axillary lymph node pain  
* axillary lymph node pain  
dysphagia  
* dysphagia  
esophageal obstruction  
* esophageal obstruction  
heart tamponade  
* heart tamponade  
pericardial effusion  
* pericardial effusion  
rib tenderness, lower  
* rib tenderness, lower  
tracheal displacement  
* tracheal displacement  
hoarseness  
* hoarseness  
digital clubbing  
* digital clubbing  
airway compression or obstruction  
* airway compression or obstruction  
Pemberton sign positive  
* Pemberton sign positive  
palms, velvet  
* palms, velvet  
Horner syndrome  
* Horner syndrome  
superior vena cava obstruction  
* superior vena cava obstruction  
bone pain  
* bone pain  
spinal cord compression  
* spinal cord compression  
supraclavicular lymph node enlargement  
* supraclavicular lymph node enlargement  
intracranial metastatic tumor  
* intracranial metastatic tumor  
acute symmetrical peripheral neuropathy  
* acute symmetrical peripheral neuropathy  
hemoptysis  
* hemoptysis  
right supraclavicular lymph node enlargement  
* right supraclavicular lymph node enlargement  
tobacco smoking  
* tobacco smoking  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
bone destruction  
* bone destruction  
chest xray unilateral diaphragm elevation  
* chest xray unilateral diaphragm elevation  
chest xray pulmonary nodule (< 4 cm), non-calcified  
* chest xray pulmonary nodule (< 4 cm), non-calcified  
chest xray mediastinal mass, adenopathy, or widening  
* chest xray mediastinal mass, adenopathy, or widening  
pleural effusion  
* pleural effusion  
pleural effusion, bloody  
* pleural effusion, bloody  
chest xray pulmonary mass (>= 4 cm), non-calcified  
* chest xray pulmonary mass (>= 4 cm), non-calcified  
hyponatremia  
* hyponatremia  
bone marrow tumor cells  
* bone marrow tumor cells  
serum calcitonin, increased  
* serum calcitonin, increased  
chest xray hilar lymph node enlargement  
* chest xray hilar lymph node enlargement  
   
   
The following findings (if present) would make this disease less likely:
The following findings (if present) would make this disease less likely:
chest xray normal  
* chest xray normal  
chest CT (contrast enhanced) normal  
* chest CT (contrast enhanced) normal  


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The following clinical manifestations (if present) would support this disease:
The following clinical manifestations (if present) would support this disease:
tendon xanthoma  
* tendon xanthoma  
xanthoma  
* xanthoma  
tuberous xanthoma  
* tuberous xanthoma  
planar xanthoma  
* planar xanthoma  
palmar planar xanthoma  
* palmar planar xanthoma  
hepatosplenomegaly  
* hepatosplenomegaly  
spleen enlargement  
* spleen enlargement  
panniculitis  
* panniculitis  
generalized diffuse lymph node enlargement  
* generalized diffuse lymph node enlargement  
   
   
The following lab data (if present) would be useful in establishing the presence of the disease:
The following lab data (if present) would be useful in establishing the presence of the disease:
ESR markedly increased  
* ESR markedly increased  
serum ferritin greatly increased  
* serum ferritin greatly increased  
ESR mildly or moderately increased  
* ESR mildly or moderately increased  
C-reactive protein elevated
* C-reactive protein elevated

Revision as of 18:12, 13 August 2015

Differential Diagnosis

The following conditions must be considered in the differential diagnosis of Hodgkin's lymphoma: DDx [1][2][3][4][5][6][7]
  • Sarcoidosis DDx
  • Lymphocytic lymphoma DDx
  • Miliary tuberculosis DDx
  • Infectious mononucleosis DDx
  • Thoracic aortic aneurysm DDx
  • Substernal goiter DDx
  • Thymoma DDx
  • Actinomycosis DDx
  • Chronic lymphocytic leukemia DDx
  • Superior vena cava syndrome DDx
  • Unicentric Castleman disease DDx
  • Adult Still disease DDx
  • Small cell lung carcinoma DDx
  • Malignant histiocytosis DDx


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Mahshid Mir, M.D. [2]

Differential Diagnosis
DDx Alphabetic Order
A B
C D
E F
G H
I J
K L
M N
O P
Q R
S T
U V
W X
Y Z


Template:WikiDoc Sources

Clinical manifestations
  • mental nerve neuropathy
  • alcohol intolerance
  • dermatitis, exfoliative
  • epitrochlear lymph node enlargement
  • inguinal lymph node enlargement
  • hepatomegaly
  • liver mass
  • superior vena cava obstruction
  • inferior vena cava obstruction
  • femoral lymph node enlargement
  • popliteal lymph node enlargement
  • Pemberton sign positive
  • fever, Pel-Ebstein
  • ascites, chylous
  • axillary lymph node enlargement
  • erythema multiforme
  • erythema nodosum
  • hepatosplenomegaly
  • mesenteric lymph node enlargement
  • paraplegia
  • pruritus
  • spinal cord compression
  • spleen enlargement
  • urinary tract obstruction
  • generalized diffuse lymph node enlargement
  • airway compression or obstruction
  • cryptococcosis
  • bone pain
  • cervical lymph node enlargement
  • fever, recurrent
  • recurrent infection
  • lymph node, fixed
  • neck mass
  • night sweats
  • anergy
  • supraclavicular lymph node enlargement
  • sweating increase
  • fever unknown origin
  • fever, remittent
  • painless lymphadenopathy
  • regional lymph node enlargement
Laboratory abnormalities
  • nucleated red cells
  • hypogammaglobulinemia
  • pancytopenia
  • lymphocytes decreased
  • granulomas on biopsy
Radiographic features
  • retroperitoneal lymph node enlargement
  • abdominal ultrasound, biliary tract dilatation
  • bone lesion
  • chest xray mediastinal mass, adenopathy, or widening
  • chest xray mediastinal mass middle
  • mediastinal lymph node enlargement
  • Anterior mediastinal mass on chest radiograph
  • gallium scan, increased uptake, abdomen
  • ivory vertebra
  • gallium scan increased uptake, mediastinum




Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3] Mahshid Mir, M.D. [4]

Differential Diagnosis
DDx Alphabetic Order
A B
C D
E F
G H
I J
K L
M N
O P
Q R
S T
U V
W X
Y Z


Template:WikiDoc Sources

Clinical manifestations
Laboratory abnormalities
Radiographic features


Evidence of "SARCOIDOSIS" (COMMON)

The following clinical manifestations (if present) would support this disease:

  • corneal deposit
  • corneal opacity
  • parotid gland swelling
  • polyneuropathy
  • cranial nerve paralysis
  • airway compression or obstruction
  • retinal granuloma
  • erythema nodosum
  • uveitis
  • ankle pain
  • facial paralysis
  • salivary gland swelling
  • splenomegaly, massive
  • cryptococcosis
  • generalized rash, papules (elevated, <0.5cm)
  • iridocyclitis
  • iritis
  • cough, dry
  • night sweats
  • spleen enlargement
  • uveitis, bilateral
  • generalized diffuse lymph node enlargement
  • polyarthritis

The following lab data (if present) would be useful in establishing the presence of the disease:

  • heart conduction abnormality, electrocardiographic
  • atrioventricular block
  • hypercalcemia
  • retroperitoneal lymph node enlargement
  • pleural effusion, lymphocytes increased
  • CXR lung cyst
  • lymphocytes decreased
  • chest xray interstitial infiltrate ( incl. reticulonodular )
  • hypercalciuria
  • alkaline phosphatase, mild-moderate elevation
  • gallium scan increased uptake, mediastinum
  • gallium scan increased uptake, lungs
  • PFT's: restrictive defect
  • PFT's: diffusion capacity decreased
  • mediastinal lymph node enlargement
  • bone marrow granulomas
  • serum angiotensin-converting enzyme elevated
  • vitamin D, 1,25-dihydroxy, increased
  • chest xray mediastinal mass, adenopathy, or widening
  • granulomas on biopsy
  • chest xray hilar lymph node enlargement

Evidence of "LYMPHOCYTIC LYMPHOMA" (COMMON)

The following clinical manifestations (if present) would support this disease:

  • mental nerve neuropathy
  • dermatitis, exfoliative
  • extremity paralysis, lower
  • gout
  • esophageal candidiasis
  • abdominal mass
  • biliary tract obstruction
  • breast mass
  • epitrochlear lymph node enlargement
  • erythema multiforme
  • erythema nodosum
  • esophageal obstruction
  • facial edema
  • gastric obstruction
  • thyroid nodule
  • hepatosplenomegaly
  • intestinal obstruction
  • intussusception
  • liver mass
  • mesenteric lymph node enlargement
  • mucous membrane bleeding
  • night sweats
  • paraplegia
  • pruritus
  • anergy
  • spinal cord compression
  • stool clay color
  • stool color yellow
  • superior vena cava obstruction
  • supraclavicular lymph node enlargement
  • testicular mass
  • urinary tract obstruction
  • inferior vena cava obstruction
  • generalized diffuse lymph node enlargement
  • splenomegaly, massive
  • femoral lymph node enlargement
  • popliteal lymph node enlargement
  • airway compression or obstruction
  • cryptococcosis
  • recurrent infection
  • lymph node, fixed
  • neck mass
  • spleen enlargement
  • fever unknown origin
  • regional lymph node enlargement
  • painless lymphadenopathy
  • cancer
  • lymphoma
  • non-Hodgkin lymphoma

The following lab data (if present) would be useful in establishing the presence of the disease:

  • IVP bladder mass or abnormal shape
  • hypercalcemia, extreme (>14 mg/dl)
  • bone destruction
  • kidney mass
  • mediastinal lymph node enlargement
  • prolonged bleeding time
  • ESR markedly increased
  • retroperitoneal lymph node enlargement
  • hypogammaglobulinemia
  • bone lesion
  • pancytopenia
  • lymphocytes decreased
  • chest xray mediastinal mass, adenopathy, or widening
  • chest xray mediastinal mass anterior
  • pleural effusion, exudate
  • bone marrow plasma cells increased
  • cryoglobulinemia
  • abdominal ultrasound, biliary tract dilatation
  • pleural effusion, lymphocytes increased
  • pleural effusion, chylous
  • malignant ascites
  • gallium scan increased uptake, mediastinum
  • gallium scan, increased uptake, abdomen
  • vitamin D, 1,25-dihydroxy, increased


The following clinical manifestations (if present) would support this disease:

  • prison inmate
  • retinal granuloma
  • erythema nodosum
  • Haiti
  • immunosuppressive therapy
  • weight loss, severe
  • corticosteroid use
  • chest pain, pleuritic
  • dyspnea, progressive
  • fever unknown origin
  • retinitis
  • tuberculosis exposure

The following lab data (if present) would be useful in establishing the presence of the disease:

  • pancytopenia
  • PPD positive
  • nucleated red cells
  • gallium scan, increased uptake, abdomen
  • abdominal CT: multiple hypodense liver lesions
  • bone marrow granulomas
  • AFB smear positive
  • chest xray multiple pulmonary nodules, non-calcified
  • granulomas on biopsy

Evidence of "INFECTIOUS MONONUCLEOSIS" (COMMON) The following clinical manifestations (if present) would support this disease:

  • optic neuritis
  • epitrochlear lymph node enlargement
  • periorbital edema
  • pharyngeal petechia
  • spleen enlargement
  • spleen palpable
  • tonsillitis
  • abdominal tenderness, left upper quadrant
  • axillary lymph node enlargement
  • inguinal lymph node enlargement
  • mesenteric lymph node enlargement
  • pharyngeal exudate
  • pharyngeal erythema
  • spleen tenderness
  • tonsillar exudate
  • generalized diffuse lymph node enlargement
  • cervical lymph node enlargement
  • pharyngeal swelling
  • sore throat

The following lab data (if present) would be useful in establishing the presence of the disease:

  • SGPT (ALT), marked elevation
  • SGPT (ALT), elevated
  • lymphocytes increased
  • atypical lymphocytes increased
  • heterophile antibody positive
  • monocytes, increased
  • Epstein-Barr virus titre positive




Evidence of "THORACIC AORTIC ANEURYSM" (RARE)

The following clinical manifestations (if present) would support this disease:

  • cocaine use
  • Turner syndrome
  • Pemberton sign positive
  • marfan syndrome
  • aortic valve regurgitation
  • superior vena cava obstruction
  • aortic dilation, ascending

The following lab data (if present) would be useful in establishing the presence of the disease:

  • chest xray mediastinal mass middle
  • chest xray mediastinal mass posterior
  • mediastinal widening
  • chest xray aorta prominent or enlarged
  • chest xray mediastinal mass anterior
  • chest xray mediastinal mass, adenopathy, or widening



Evidence of "SUBSTERNAL GOITER" (RARE)

The following clinical manifestations (if present) would support this disease:

  • upper extremity edema
  • chest mass
  • neck mass
  • thyroid enlargement
  • tracheal compression
  • Pemberton sign positive

The following lab data (if present) would be useful in establishing the presence of the disease:

  • TSH elevated
  • chest xray mediastinal mass, adenopathy, or widening
  • chest xray mediastinal mass anterior

Evidence of "THYMOMA" (RARE)

The following clinical manifestations (if present) would support this disease:

  • bulbar palsy
  • facial candida infection
  • facial cyanosis
  • jugular venous distention
  • mouth candida infection
  • superior vena cava obstruction
  • diplopia
  • Pemberton sign positive

The following lab data (if present) would be useful in establishing the presence of the disease:

  • pancytopenia
  • antistriational antibodies
  • chest xray mediastinal mass, adenopathy, or widening
  • chest xray mediastinal mass anterior




Evidence of "ACTINOMYCOSIS" (RARE) The following clinical manifestations (if present) would support this disease:

  • tongue mass
  • trismus
  • pericardial constriction
  • pharyngeal swelling
  • pharyngeal tenderness
  • abdominal fistula
  • bronchial fistula
  • empyema
  • lung abscess
  • abdominal mass, right lower quadrant
  • chest wall suppuration
  • gingival fistula
  • chest wall fistula
  • gingival swelling
  • gingival tenderness
  • jaw induration
  • mandibular swelling

The following lab data (if present) would be useful in establishing the presence of the disease:

  • echocardiogram: intracardiac mass
  • hepatic cyst(s)
  • mediastinal lymph node enlargement
  • chest xray mediastinal mass, adenopathy, or widening
  • Gram stain: branching Gram-positive bacilli
  • sulfur granule


Evidence of "CHRONIC LYMPHOCYTIC LEUKEMIA" (RARE)

The following clinical manifestations (if present) would support this disease:

  • skin infiltration
  • sternal tenderness
  • lymph node firmness

The following lab data (if present) would be useful in establishing the presence of the disease:

  • hemolysis
  • mediastinal lymph node enlargement
  • prolonged bleeding time
  • chest xray mediastinal mass, adenopathy, or widening
  • monoclonal gammopathy
  • cryoglobulinemia
  • leukocytes, marked increase
  • flow cytometry: clonal B-lymphocytes
  • lymphocytes increased

The following findings (if present) would make this disease less likely:

  • left shift
  • metamyelocytes increased

Evidence of "SUPERIOR VENA CAVA SYNDROME" (RARE - Urgent action required) The following clinical manifestations (if present) would support this disease:

  • stridor
  • facial erythema
  • forehead vein distention
  • lymphoma
  • tracheal displacement
  • chest vein distention
  • facial cyanosis
  • collateral circulation increase
  • conjunctival edema
  • conjunctival vein distention
  • upper extremity edema
  • upper extremity erythema
  • head edema
  • jugular venous distention with inspiration
  • lung tumor
  • extremity cyanosis
  • upper extremity vein distention
  • facial edema
  • neck edema
  • jugular venous distention
  • lung cancer
  • upper extremity cyanosis
  • facial vein distention
  • superior vena cava obstruction

The following lab data (if present) would be useful in establishing the presence of the disease:

  • mediastinal lymph node enlargement
  • chest xray pulmonary nodule (< 4 cm), non-calcified
  • chest xray mediastinal mass, adenopathy, or widening

The following findings (if present) would exclude this disease:

  • hepatojugular reflux

Evidence of "UNICENTRIC CASTLEMAN DISEASE" (RARE)

  • The following lab data (if present) would be useful in establishing the presence of the disease:
  • mediastinal lymph node enlargement
  • chest xray mediastinal mass, adenopathy, or widening

Evidence of "ADULT STILL DISEASE" (RARE)

The following clinical manifestations (if present) would support this disease:

  • ankylosis
  • hepatosplenomegaly
  • weight loss, severe
  • fever, recurrent
  • night sweats
  • wrist pain
  • generalized diffuse lymph node enlargement
  • fever unknown origin
  • fever, remittent
  • fever, high grade
  • polyarticular
  • rash, evanescent

The following lab data (if present) would be useful in establishing the presence of the disease:

  • leukocytes, marked increase
  • ESR markedly increased
  • serum ferritin greatly increased

The following findings (if present) would make this disease less likely:

  • monoarticular

The following findings (if present) would exclude this disease:

  • asymptomatic

Evidence of "SMALL CELL LUNG CARCINOMA" (COMMON)

The following clinical manifestations (if present) would support this disease:

  • acanthosis nigricans
  • axillary lymph node enlargement
  • axillary lymph node pain
  • dysphagia
  • esophageal obstruction
  • heart tamponade
  • pericardial effusion
  • rib tenderness, lower
  • tracheal displacement
  • hoarseness
  • digital clubbing
  • airway compression or obstruction
  • Pemberton sign positive
  • palms, velvet
  • Horner syndrome
  • superior vena cava obstruction
  • bone pain
  • spinal cord compression
  • supraclavicular lymph node enlargement
  • intracranial metastatic tumor
  • acute symmetrical peripheral neuropathy
  • hemoptysis
  • right supraclavicular lymph node enlargement
  • tobacco smoking

The following lab data (if present) would be useful in establishing the presence of the disease:

  • bone destruction
  • chest xray unilateral diaphragm elevation
  • chest xray pulmonary nodule (< 4 cm), non-calcified
  • chest xray mediastinal mass, adenopathy, or widening
  • pleural effusion
  • pleural effusion, bloody
  • chest xray pulmonary mass (>= 4 cm), non-calcified
  • hyponatremia
  • bone marrow tumor cells
  • serum calcitonin, increased
  • chest xray hilar lymph node enlargement

The following findings (if present) would make this disease less likely:

  • chest xray normal
  • chest CT (contrast enhanced) normal

Evidence of "MALIGNANT HISTIOCYTOSIS" (RARE)

The following clinical manifestations (if present) would support this disease:

  • tendon xanthoma
  • xanthoma
  • tuberous xanthoma
  • planar xanthoma
  • palmar planar xanthoma
  • hepatosplenomegaly
  • spleen enlargement
  • panniculitis
  • generalized diffuse lymph node enlargement

The following lab data (if present) would be useful in establishing the presence of the disease:

  • ESR markedly increased
  • serum ferritin greatly increased
  • ESR mildly or moderately increased
  • C-reactive protein elevated
  1. Ferri, Fred (2011). Ferri's differential diagnosis: a practical guide to the differential diagnosis of symptoms, signs, and clinical disorders. Philadelphia, PA: Elsevier/Mosby. ISBN 978-0323076999.
  2. Siegenthaler, Walter (2007). Differential diagnosis in internal medicine: from symptom to diagnosis. Stuttgart New York: Thieme. ISBN 978-1588905512.
  3. Mesko, Dusan (2002). Differential diagnosis by laboratory medicine: a quick reference for physicians. Berlin New York: Springer-Verlag. ISBN 978-3540430575.
  4. Reeder and Felson's gamuts in radiology: comprehensive lists of roentgen differential diagnosis. Place of publication not identified: Springer. 2014. ISBN 978-1475781229.
  5. Burgener, Francis (2008). Differential diagnosis in conventional radiology. Stuttgart New York: Thieme. ISBN 978-1588902757.
  6. Gattuso, Paolo (2015). Differential diagnosis in surgical pathology. Philadelphia, PA: Saunders/Elsevier. ISBN 978-1455770137.
  7. "DXplain".