Difference between revisions of "Hereditary breast cancer"
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Revision as of 15:49, 27 May 2014
This article deals with hereditary breast cancer.
Syndromes associated with breast cancer
Gene | Syndrome | Other cancers | Notes |
---|---|---|---|
BRCA1 | Familial breast and ovarian cancer[1] | male breast, ovarian, prostate, pancreas, fallopian tube | younger individuals vis-à-vis BRCA2 |
BRCA2 | Familial breast and ovarian cancer 2[2] | male breast, ovarian, prostate, pancreas, stomach, melanoma, gallbladder, bile duct, pharynx | older individuals vis-à-vis BRCA1 |
TP53 (p53) | Li-Fraumeni syndrome (AKA SBLA syndrome) | sarcomas, brain cancer, larynx, lung, leukemia, adrenal cortical carcinoma | often present in childhood |
CHEK2 | Li-Fraumeni syndrome (variant) | see p53 | - |
STK11 | Peutz-Jeghers syndrome | breast cancer, GI cancer, Sertoli cell tumour, Granulosa cell tumour, SCTAT | characteristic GI hamartomas, mucocutaneous pigmentation |
PTEN | Cowden syndrome | breast, thyroid (PTC), endometrial, renal, colorectal | - |
CDH1 | Familial diffuse gastric cancer[3] | invasive lobular carcinoma, gastric signet ring cell carcinoma | - |
BRCA1 and BRCA2
BRCA1 vs. BRCA2:[4]
Gene | Age | Histology | Other cancers |
---|---|---|---|
BRCA1 | younger | worse types, e.g. triple negative breast ca. | uterine tube |
BRCA2 | older | sporadic types | stomach, melanoma, gallbladder, bile duct, pharynx |
Types of cancer associated with both BRCA1 and BRCA2 - male OPP:
- Male breast, ovarian, prostate, pancreas.
How to remember types of cancer associated with BRCA2 - PUM:
- Pharynx, upper GI (stomach, gallbladder, biliary), melanoma.
See also
References
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 113705
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 600185
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 192090
- ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1078. ISBN 978-1416031215.