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A Case of Leiomyosarcoma of the Duodenum M. Kawakami 1 , M. Takahashi 1 , F. Yanagisawa 1 , S. Shindo 1 , S. Ashizawa 1 1Dept. of Internal Medicine, Tokyo Medical College pp.1654-1658
Published Date 1973/12/25
DOI https://doi.org/10.11477/mf.1403108418
  • Abstract
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 Leiomyosarcoma of the duodenum is not so common, and it was rarely diagnosed preoperatively. Recently we encountered one case, so report it in this paper.

 A 24-year-old female patient was admitted to our hospital with the chief complaint of teery stool appeared four times a year since the end of December, 1971.

 On admission, she was found to be slightly anemic. but had no other abnormal signs. No abnormality was seen in the routine upper and lower GI x-ray examinations. At last we have done newly developed small-intestinalfiberscopy (SIF), and then we have found diffuse bleeding at the third portions of the duodenum.

 Retrospective hypotonic-duodenography revealed a tumor shadow with central barium freck there. The second SIF found a protruded region rising straightly in the lumen, and having same color of normal intestinal membranes and like bridging-folds. The clinical diagnosis was made suspicion of submucosal (perphaps malignant) tumor. At laparotomy, the tumor was localized to the third of the duodonum with no metastatic finding of liver and other abdominal lymph nodes.

 The tumor size was 1.8×1.4 cm large and 2.0 cm height with deep depression. Histologically, the tumor was diagnosed as leiomyosarcoma.

 The case is the 52 nd case in Japan from 1939 to 1971, and 93 cases were reported in foreign countries from 1920 to 1971. But our case is the most smallest tumor in the world literature. The patient is now living and well 6 months after operation with no evidence of metastic signs.


Copyright © 1973, 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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