Dergiler / Acta Medica Nicomedia / 1997 / Cilt: 2 Sayı: 2

Gardner Sendromu: Olgu Sunumu

Gardner Syndrome: Case Report

Altay ÇELEBİ, Ömer ŞENTÜRK, Dilek BAYRAMGÜRLER, Ergun VELİDEDEOĞLU, Hülya DAL, Saadettin HÜLAGÜ

Sayfa
45–47
DOI
—

Özet

Ailesel adenomatöz polipozis koli sendromları; kolonda yüzlerce-binlerce adenomatöz poliple karakterize, nadir görülen, otozomal dominant geçişli sendromlardır. Gardner sendromundaki ekstraintestinal bulgular; osteomalar, yumuşak doku tümörleri, tiroid ve adrenal tümörleri ve retinal pigment epitel hipertrofisidir. Tedavi cerrahidir.

Abstract

Familial Adenomatous Polyposis Coli (FAPC) Syndromes are rare dominantly inherited syndromes characterized by hundreds to thousands of colonic adenomatous polyps. Extraintestinal abnormalities of Gardner syndrome are osteomas, soft tissue tumors, thyroid and adrenal tumors, hypertrophy of the retinal pigment epithelium. Management of FAPC is surgery

Anahtar kelimeler: Gardner sendromu