Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic, malignant breast tumor characterized by early onset breast cancer in association with a germline mutation. Tumors arising in carriers of <i>BRCA1</i> and <i>BRCA2</i> mutations differ morphologically and genetically from each other, as well as from sporadic breast cancers. Most <i>BRCA1</i>-associated tumors are invasive ductal adenocarcinomas of no special type, typically of higher grade than sporadic tumors, and more often negative for hormone receptors. In addition, more cases with features of typical or atypical medullary carcinoma are seen in these patients. Likewise, <i>BRCA2</i>-associated tumors tend to be of higher grade than sporadic ones, although their phenotype is similar. They show a low frequency of HER-2 expression. Dane Klasyfikacja Choroba Synonimy Familial breast cancer Rodzinny rak piersi Familial breast carcinoma Hereditary breast carcinoma Kod ORPHA 227535 Kod OMIM 613399 Kod ICD10 C50.0 Kod ICD11 2C6Y *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl