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Localized Amyloidosis of the Stomach, Report of a Case Shigeto Yoshida 1 , Tohru Hidaka 1 , Hiroaki Ohgoshi 1 , Taneomi Okuhara 1 , Yuzo Hayashi 2 1Department of Internal Medicine, Hiroshima City Asa Hospital 2Department of Pathology, Hiroshima City Asa Hospital Keyword: 限局性胃アミロイドーシス pp.119-124
Published Date 1998/1/25
DOI https://doi.org/10.11477/mf.1403103563
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 A 69-year-old woman was admitted to our hospital suffering from left flank pain. Radiological examination of the gastrointestinal tract showed an irregular, mucosal pattern in the antrum. Endoscopic examination revealed discoloration, redness and coarse mucosa in the antrum. Histological examination of biopsy specimens revealed no malignancy. Four years later, distension of the antrum was revealed in a radiology examination. Endoscopic examination showed a coarse mucosal pattern in the antrum, and biopsy specimens revealed amyloidosis of the stomach. Seven years later, endoscopic findings were unchanged. Eight years after the first medical examination, the patient died of cholangiocellular carcinoma at another hospital. Autopsy was performed, and histological examination showed amyloid deposits in the antrum, but not in any other organs. Based on these findings, this case was diagnosed as localized amyloidosis of the stomach.


Copyright © 1998, 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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