Gardner Sendromu: Olgu Sunumu

Year 1997, Volume: 2 Issue: 2, 45 - 47, 30.04.1997

Altay Çelebi Ömer Şentürk Dilek Bayramgürler Ergun Velidedeoğlu Hülya Dal Saadettin Hülagü

Abstract

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.

Keywords

Gardner sendromu

Gardner Syndrome: Case Report

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

Keywords

Gardner syndrome

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