Gardner sendromu: Olgu sunumu

Year 2007, Volume: 6 Issue: 2, 86 - 89, 01.08.2007

Berna Bayrakçı Erdal Özen Ahmet Sever A. Ömer Özütemiz

Abstract

Gardner sendromu polipozis koli, çok sayıda osteom ve cilt ve yumuşak dokuda mezenşimal tümör varlığı ile tanımlanmış otozomal dominant kalıtım gösteren bir hastalıktır ve nadir olarak görülür. Polipozis koli malign transformasyon için çok yüksek risk taşır. Bu nedenle erken tanı ve tedavisi önemlidir. Osteom kemik dokunun benign tümörüdür ve yavaş büyüme özelliğine sahiptir, üç veya daha fazla osteom saptandığında Gardner sendromu araştırılmalıdır. Cilt bulguları epidermoid kist, desmoid tümör ve diğer benign tümörleri içermektedir. Biz bu yazıda polipozis koli, osteom ve epidermoid kistleri saptanan Gardner sendromu tanılı 36 yaşındaki bir erkek olguyu sunuyoruz.

Keywords

Gardner sendromu, osteom, epidermoid kist, cerrahi tedavi

Gardner's syndrome: A case report

Abstract

Gardner syndrome is a rare autosomal dominant disease characterized by the presence of colonic polyposis, osteomas and a multitude of soft tissue tumors. Colonic polyposis has a very high risk of undergoing malignant transformation; consequently, early identification and therapy of the disease are important. Osteoma is a benign neoplasm of bone tissue and it is characterized by slow continuous growth. A finding of three or more osteomas is investigated as Gardner syndrome. Cutaneous findings include epidermoid cyst, desmoid tumors, and other benign tumors. We present a case of a 36-yearold male patient with Gardner syndrome who presented with colonic polyposis, osteomas and epidermoid cysts.

Keywords

Gardner's syndrome, osteoma, epidermoid cyst, surgical treatment

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