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Duodenal Carcinoid, a Case Report T. Konno 1 , S. Tashiro 1 , M. Tanaka 1 , I. Yokoyama 1 , K. Sakai 2 1First Department of Surgery, Kumamoto University Medical School 2Second Department of Pathology, Kumamoto University Medical School pp.1153-1158
Published Date 1976/9/25
DOI https://doi.org/10.11477/mf.1403107426
  • Abstract
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 A 68-year-old woman was admitted with chief complaints of epigastralgia and tarry stool. There was no Carcinoid syndrome in her history. Barium enema and endoscopic examination of the upper gastrointestinal tract revealed a submucosal tumor in the second portion of the duodenum. Celiac angiogram showed remarkable vascular neoformation arising from the gastroduodenal artery. A well-defined 4×2.5 cm sized dense tumor stain was observed. Dilated and regular draining veins were observed. Urine 5-HIAA levels were not elevated. A submucosal solid tumor, 3.5×2.4×2.0 cm, wes removed. Its cut surface showed yellow-brown color. Microscopic examination revealed Carcinoid composed of tumor cells of uniform size with island-like, cord-like or rosette-like structures.

 Both argyrophil reaction by Sevier-Munger method and argentaffin reaction by Fontana-Masson method were negative.


Copyright © 1976, 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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