Sandbox:Shadan: Difference between revisions

Jump to navigation Jump to search
Line 169: Line 169:
*Weight loss
*Weight loss


 
{{Family tree/start}}
{{Family tree/start|||||||||||||||||||||||||||A0= breast lumps symtoms||||||||||||||||||||||||||}}
{{Family tree|||||||||||||||||||||||||||A01= breast lumps symptoms||||||||||||||||||||||||||}}
{{Family tree||||||||||||||||||||||||||-|-|-|-|!|-|-|-|||||||||||||||||||||||||}}
{{Family tree||||||||||||||||||||||||||-|-|-|-|!|-|-|-|||||||||||||||||||||||||}}
{{Family tree|||||||||||||||||||||||||||||||||||||||||||||||||||||||||}}
{{Family tree|||||||||||||||||||||||||||||||||||||||||||||||||||||||||}}

Revision as of 16:29, 7 December 2018


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

Overview

Classification

Classification of breast lumps based on epithelial hyperplasia[1]

  • Approximately 65% of all benign breast disease considered as nonproliferative(NP)with relative cancer risk of 1.2, 1.4 times:
    • Simple cyst
    • Fibrosis
    • Fibroadenoma (simple)
    • Columnar alteration (Simple)
    • Apocrine metaplasia (simple)
    • Mild ductal hyperplasia
  • Approximately 30% of total are classifed as proliferative disease(PD) with relative cancer risk of 1.7, 2.1 times
    • Usual ductal hyperplasia
    • Sclerosing adenosis
    • Columnar hyperplasia
    • papilloma
    • Radical scar
  • Approximately 5% to 8% of the rest regarded to PD with atypia with relative cancer risk more than 4 times
    • Atypical lobar hyperplasia
    • Lobular carcinoma in situ
    • Atypical ductal hyperplasia
  • Unclear risk
    • Mucocele like tumor
    • Apocrine atypia
    • Secretory atypia

Classification of benign breast lesion regarding to histological region:[2]

  • Terminal and lobular ducts
    • Acinar distention
      • Cyst
    • Intralobular connective tissue proliferation
      • Sclerosing adenosis
      • Fibroadenoma
      • Phyllodes tumor
      • Hamartoma
    • Epithelial changes in terminal duct lobaular units (TDLU)
      • Apocrine metaplasia
      • Ductal and lobular hyperplasia, usual and typical
      • Papillomatosis
      • Intracystic papilloma
  • Ductal system
    • Ductal ectasia
    • Intraductal papilloma
  • Lesion of different origin
    • Fatty tissue lesion
      • Lipoma
      • Liponecrosis
    • Fibrous tissue lesions
      • Focal fibrosis
      • Diabetic mastopathy
      • Pseudoangiomatous stromal hyperplasia (PASH)
      • Myofibroblastoma
    • Vascular origin
      • Hemangioma
    • Inflammatory origin
      • Mastitis/abscess
      • Tuberclosis and sarcoidosis
      • Foreign body granuloma and siliconoma
    • Lymph node origin
      • Inflammatory lymoh nodes

Risk factors

Associated risk factors leading to female breast cancer[3]

  • 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.
  • Personal history of breast cancer
  • Breast pathology: PD with atypia has greater risk of developing to breast cancer in comparison of PD.
  • Family history: greater breast cancer risk in women with first degree relatives with breast cancer under 50 years old.
  • Genetic predisposition
    • High risk
      • BRCA1
      • BRCA2
    • Moderate risk
      • Homozygous ataxia-telangiectasia (ATM)
      • Somatic mutation in CHEK2
      • BRCA1 modifier gene: BRIP1
      • BRCA2 modifier gene: PALB2
    • Low risk
      • These alleles have not designated yet.

Endogenous hormone exposure and reproductive factors:

  • Early menarche;under age of 13 years
  • Parity; nulliparous is associated with incresed risk of breast cancer
  • Age at first full term pregnancy; younger age may decrease risk of breast cancer
  • Breast feeding; decreased risk of breast cancer
  • Testostrone; increased relative risk to 2.86-3.28
  • Age at menopause;older menopausal age associated with greater risk of breast cancer

Exogenous hormone exposure

  • long term exposure> 5 years; increases chances of breast cancer
  • Time of usage;nearly menopausal age associated with development to breast cancer

Lifestyle These factors may increase risk of developing breast cancers

  • Alcohol consumption; even as 5.0 to 9.9 per day, approximately 3 to 6 drinks per week, developed with relative risk 1.15
  • Inactivity
  • Obesity; BMI:25-29.9 and BMI>30 have relative risk about 1.28
  • Previous history of radiation;at the age< 35years old

Screening

The Screening methods of breast lesions[3]:

  • 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 [4]
  • 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 [3]

  • 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

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

References

  1. Hartmann LC, Sellers TA, Frost MH, Lingle WL, Degnim AC, Ghosh K; et al. (2005). "Benign breast disease and the risk of breast cancer". N Engl J Med. 353 (3): 229–37. doi:10.1056/NEJMoa044383. PMID 16034008.
  2. Lanyi, M (2003). Mammography : diagnosis and pathological analysis. Berlin New York: Springer-Verlag. ISBN 9783540441137.
  3. 3.0 3.1 3.2 Shah R, Rosso K, Nathanson SD (2014). "Pathogenesis, prevention, diagnosis and treatment of breast cancer". World J Clin Oncol. 5 (3): 283–98. doi:10.5306/wjco.v5.i3.283. PMC 4127601. PMID 25114845.
  4. Kelly KM, Dean J, Comulada WS, Lee SJ (2010). "Breast cancer detection using automated whole breast ultrasound and mammography in radiographically dense breasts". Eur Radiol. 20 (3): 734–42. doi:10.1007/s00330-009-1588-y. PMC 2822222. PMID 19727744.