Gardner Sendromu: Olgu Sunumu

Yıl 1997, Cilt: 2 Sayı: 2, 45 - 47, 30.04.1997

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

Öz

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.

Anahtar Kelimeler

Gardner sendromu

Gardner Syndrome: Case Report

Öz

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 syndrome

Kaynakça

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