| Literature DB >> 19537128 |
Antonino Versaci1, Antonio Macrì, Maddalena Grosso, Marialuisa Terranova, Grazia Leonello, Antonio Ieni, Giovanna Rivoli, Ciro Famulari.
Abstract
The authors report on a case of voluminous perforated gastrointestinal stromal tumor (GIST) of small intestine and make a review to the light of most recent clinicopathologic advancements. The first clinical manifestation as acute abdomen due to their perforation extremely rare. Gastrointestinal stromal tumor (GIST) represent a rare group of multiform tumors with various biological behaviour. Were identified in the past as leiomyomas, leiomyosarcomas or leiomyoblastomas, has been reclassified on immunochemical features, with a positive expression of Kit (CD117 antigen). Traditionally the prognostic factors of these tumour are: mitotic rate, tumor size and anatomic site. The complete surgical resection and use of imatinib mesylate (Gleevec) are the best available approach.Entities:
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Year: 2009 PMID: 19537128
Source DB: PubMed Journal: Ann Ital Chir ISSN: 0003-469X Impact factor: 0.766