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Japanese

Membranous Atresia of the Cecum, Report of a Case Kazunari Ishii 1 , Kazunori Maeda 1 , Tomohiko Nishihira 2 , Satoshi Ohnishi 2 , Kanzo Fukuma 3 1Department of Radiplogy, National Himeji Hospital 2Department of Surgery, National Himeji Hospital 3Department of Internal Medicine, National Himeji Hospital Keyword: 盲腸膜様閉鎖症 , 先天性結腸閉鎖 pp.693-696
Published Date 1991/6/25
DOI https://doi.org/10.11477/mf.1403102567
  • Abstract
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 A 75-year-old man was admitted to our hospital complaining of right lower abdominal discomfort. A plain film of the abdomen demonstrated a calcified shadow like a fecal stone in the right lower area of the abdomen. Barium enema showed this mass was outside of the colon and appendix was not demonstrated. Colonofiberscopy showed that it resembled a submucosal tumor. The resected cecum revealed that the cecum was separated from the ascending colon with a membrane with normal mucosa, communicating with the ascending colon by a small hole, and filled with barium feces. It was diagosed as a congenital membranous atresia of the cecum. Most reports support the vascular theory as the cause of colonal atresia but this case supports the recanalization-disturbance theory.


Copyright © 1991, 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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