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Colorectal Leiomyosarcoma – a Rare Tumour in GIST Era Cover

Colorectal Leiomyosarcoma – a Rare Tumour in GIST Era

Open Access
|Sep 2015

Abstract

Primary malignant mesenchymal colorectal tumours, representing a small fraction of soft tissue sarcomas, are characterised by predominance of gastrointestinal stromal tumour (GIST). After the GIST concept has been implemented in the diagnostics, the incidence of registered leiomyosarcomas has markedly decreased. The scarcity of credible cases embarrasses the analysis of tumour biological behaviour. Here we report well-documented, immunohistochemically proved, surgically treated case of colonic leiomyosarcoma (LMS) in order to broaden the published evidence by our data and to emphasize that the differential diagnosis of mesenchymal gastrointestinal tumours is not limited by GIST.

DOI: https://doi.org/10.1515/chilat-2015-0007 | Journal eISSN: 2199-5737 | Journal ISSN: 1407-981X
Language: English
Page range: 36 - 39
Published on: Sep 1, 2015
Published by: Riga Stradins University
In partnership with: Paradigm Publishing Services
Publication frequency: 1 times per year

© 2015 Inese Drike, Ilze Strumfa, Lubova Kolomencikova, Ervins Vasko, Andrejs Vanags, Janis Gardovskis, published by Riga Stradins University
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.