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Familial Juvenile Polyposis Coli, Report of a Case Shimako Yamamoto 1 1The Second Department of Internal Medicine, Faculty of Medicine, Kyushu University Keyword: 消化管ポリポーシス , 若年性ポリポーシス , 家族性若年性大腸ポリポーシス , 癌化 pp.1373-1377
Published Date 1993/11/25
DOI https://doi.org/10.11477/mf.1403106323
  • Abstract
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 A 17-year-old boy visited our hospital because of anal bleeding. Barium enema radiography and colonoscopy showed multiple sessile or pedunculated polyps in the colon and rectum, predominantly in the sigmoid colon and rectum. The polyp had a smooth, reddish surface. Twelve polyps were removed endoscopically. All of these polyps were histologically compatible with juvenile polyposis. There was no polyp in the oter parts of the gastrointestinal tract.

 Family history revealed that the patient's father and younger brother had undergone endoscopic polypectomy for colonic juvenile polyps. The diagnosis of familial juvenile polyposis coli was confirmed. In addition, his father, uncle, and grandfather had suffered from rectal cancer. Therefore, patients with familial juvenile polyposis coli are considered to require careful periodic gastrointestinal examination because of the high risk of colonic cancer.


Copyright © 1993, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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