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Reactive Lymphoreticular Hyperplasia with Remarkable Narrowing of the Antrum, Report of a Case M. Fujiwara 1 , M. Nomura 1 , J. Shibata 1 , Y. Noso 2 , H. Matsuura 3 1Department of Internal Medicine, Hiroshima City Hospital 2Department of Surgery, Hiroshima City Hospital 3Department of Pathology, Hiroshima City Hospital pp.965-969
Published Date 1982/9/25
DOI https://doi.org/10.11477/mf.1403108809
  • Abstract
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 A 78-year-old man had epigastric distress since 1973, and gastrocamera was performed in 1973 and 1975.

 X-ray picture performed in 1980 disclosed two niches on the angulus without malignant findings and remarkable narrowing of the antrum, which was uncertain in nature.

 Gastrocamera studies without biopsy performed in 1973 and 1975 showed benign ulcers on the angulus. Gastrofiberscopic findings in 1980 revealed two peptic ulcers and narrowing of the antrum with some erosions. But precise observation on the antrum was impossible because of tunnel formation. Biopsy specimens of the ulcers and the erosions of the antrum were classified into group II.

 The surgically resected specimen showed two ulcers on the angulus and remarkable thickness (1.5 cm) of the antrum wall, which was pale, yellow.

 Histopathologically, peptic ulcers were ulcus-IV, and growth of lymph follicles was found mainly in the muscle layer and the subserosa ann scarcely in the propria mucosa and the submucosa in the antrum to the oral side of the ulcers. Therefore the lesion was diagnosed as RLH due to the peptic ulcers on the angulus.

 Thickness of the muscle layer of the antrum due to RLH was a first report in Japanese literature.


Copyright © 1982, 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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