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Lipoma of Stomach Associated with Atypical Epithelium of Overlying Mucosa, Report of a Case M. Takami 1 , M. Hanada 2 , M. Kimura 1 , N. Takeuchi 1 , T. Maeda 1 , T. Nakazima 3 , K. Otori 4 , M. Takemura 5 , M. Honda 6 1Department of Surgery, Toyonaka Municipal Hospital 2Department of Pathology, Toyonaka Municipal Hospital 3Department of Internal Medicine, Toyonaka Municipal Hospital 4Department of Internal Medicine, Osaka Kaisei Hospital 5Department of Surgery, Osaka Kaisei Hospital 6Department of Pathology, Osaka Kaisei Hospital pp.1219-1226
Published Date 1980/11/25
DOI https://doi.org/10.11477/mf.1403112784
  • Abstract
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 A case of gastric lipoma in a 52 year-old man is reported in which its overlying mucosa was accompanied by “atypical epithelium”. The patient was asymptomatic, and the lesion was incidentally found by routine x-ray examination of the stomach for his health care. Both radiologically and endoscopically, the lesion appeared as a semi-pedunculated polypoid lesion at the anterior wall of the lower body, and resembled either hyperplastic polyp or early carcinoma, Type Ⅰ.

 Biopsy showed glandular changes typical of “atypical epithelium”, but small foci suggestive of tubular adenocarcinoma were seen, which could be interpreted as Group Ⅳ. The patient refused surgery, so that it was decided to perform an endoscopic polypectomy.

 The polypectomy specimen showed on cut section a well-circumscribed lipoma, measuring 17×10×10 mm, lying in the submucosa, which was completely resected. Histologically, its overlying mucosa looked like that seen in the previous biopsy specimens. It was entirely covered with slightly elevated mucosa of “atypical epithelium”. Focal areas suggestive of adenocarcinoma, as evidenced by occasional formation of intaglandular budding and marked stratification of nuclei with loss of polarity. were superficially seen as well as transformed more typical areas of “atypical epithelium”, without no clear-cut demarcation between these two areas.

 One year follow-up with repeated endoscopic examinations showed no abnormalities. No similar case was to be found in the Japanese literature.


Copyright © 1980, 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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