Literature DB >> 11319460

[Gastrointestinal stromal tumors].

M J Boudet1, P De Mestier.   

Abstract

There are two main types of gastrointestinal connective tissue tumors: differentiated connective tissue tumors arising from smooth muscle tissue, schwanommas or fibroblastic tissue, and non-differentiated connective tissue tumors with no precise origin. Pathologically non-classifiable tumors comprise a group of real gastrointestinal stromal tumors. Stromal tumors are rare and generally develop in the stomach. Immunohistochemistry has been able to identify three entities: stromal tumorswith skenoid fibers, gastoinestinal autonomic nerve tumors, and intraabdominal desmoplastic small round-cell tumors. After resection, survival is almost 50% at 5 years and depends particulary on tumors size, the presence of synchronous metastases and mitosis count.

Entities:  

Mesh:

Year:  2001        PMID: 11319460

Source DB:  PubMed          Journal:  J Chir (Paris)        ISSN: 0021-7697


  2 in total

Review 1.  Treatment of gastrointestinal stromal tumors with imatinib mesylate: a major breakthrough in the understanding of tumor-specific molecular characteristics.

Authors:  Philippe de Mestier; Gaetan des Guetz
Journal:  World J Surg       Date:  2005-03       Impact factor: 3.352

Review 2.  [Gastrointestinal Stromal Tumors "GIST": status and news through our experience on 54 cases and review of literature].

Authors:  Nezha Taoufiq; Asmaa Naim; Zineb Bouchbika; Nadia Benchekroune; Hassan Jouhadi; Souha Sahraoui; Abdelatif Benider
Journal:  Pan Afr Med J       Date:  2017-06-30
  2 in total

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