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- W2129820007 abstract "Gardner syndrome is a variant of the familial adenomatous polyposis syndrome. We describe a case of Gardner syndrome with clinical manifestations including colonic and gastric polyposis, colon adenocarcinoma, abdominal desmoid tumor, and skull osteomas. A 37-year-old woman suffered from intermittent epigastric dull and cramping pain for one week. Moreover, poor appetite and vomiting after medication and no stool passage were also noted. An abdominal computed tomography (CT) revealed infiltrative tumor at hepatic flexure of colon and two tumor masses at abdominal wall. Colonoscopy showed polyposis and the biopsy showed tubular adenoma. The patient underwent surgical intervention. Colon adenocarcinoma, adenomatous polyposis of colon, and abdominal wall desmoid tumors were diagnosed. Three months later, the patient suffered from upper gastrointestinal (UGI) bleeding and conscious change. UGI endoscope study revealed gastric polyposis and a brain CT survey showed multiple osteomas. The diagnosis of Gardner syndrome was made according to these clinical manifestations. Physicians should be aware of this diagnosis and further evaluation is needed if any of the clinical manifestations of Gardner syndrome is found. Gardner syndrome is a variant of the familial adenomatous polyposis syndrome [1]. This disease is characterized by the presence of familial adenomatous polyposis, benign osteomas, and skin and soft tissue tumors [1, 2]. We describe a case of Gardner syndrome with clinical manifestations including colonic and gastric polyposis, colon adenocarcinoma, abdominal desmoid tumor, and skull osteomas." @default.
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- W2129820007 date "2008-03-01" @default.
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- W2129820007 title "A Young Female Patient with Gardner Syndrome: A Case Report" @default.
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