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Clinical Aspects of Gastrointestinal Stromal Tumor (GIST) Motohisa Takami 1 , Junya Fujita 1 , Yasuo Tsukahara 1 , Takashi Shibata 1 , Yukio Fukushima 1 1Department of Surgery, Toyonaka Municipal Hospital Keyword: GIST , 筋原性腫瘍 , c-kit , 消化管間葉性腫瘍 , Cajalの介在細胞 , Cajalの介在細胞 pp.1147-1156
Published Date 2001/8/25
DOI https://doi.org/10.11477/mf.1403103297
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 The term “gastrointestinal stromal tumor (GIST)” was introduced as a histogenetically neutral term referring to the main group of mesenchymal tumors of the digestive tract, which could be verified neither as neurogenic nor as myogenic in origin. Recent studies indicate that the majority of mesenchymal tumors of the gestrointestinal tract form a biologically distinctive group.

 The most practicable diagnostic criteria for GIST is the immunohistochemically determined c-kit (CD117) expression.

 According to the above concepts, we analysed a total of 30 gastric and 26 small intestinal (including 7 duodenal) cases of GIST, which were encountered in Toyonaka Municipal Hospital.

 In our series, about 10% of gastric and 30% of small intestinal cases of GIST were estimated as having high-grade malignancy with no lymphnode metastasis. All cases of high-grade GIST died within a few months after operation due to hepatic or peritoneal metastases.

 A large majority of low-grade GIST showed a clinically good course and only one patient with low-grade duodenal GIST died due to hepatic metastasis and local recurrence, 11 years after the operation.

 At present, we have a few way to control hematogenous metastasis of malignant GIST, so minimal operations (local or partial resection) are preferred for these tumors.


Copyright © 2001, 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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