Gastrointestinal stromal tumors

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Marco Pericoli Ridolfini
Alessandra Cassano
Riccardo Ricci
Fabio Rotondi
Stefano Berardi
Giacomo Cusumano
Fabio Pacelli
Giovanni Battista Doglietto

Abstract

Gastrointestinal Stromal Tumor (GIST) account for 1% of all gastrointestinal neoplasms and are the most common mesenchymal tumor of gastrointestinal tract. There are considered to originate from the intestinal cell of Cajal, an intestinal pacemaker cell, characterized usually express the KIT protein on immunohistochemistry. The stomach (40-60%) and small intestine (30-40%) are the most common locations. Diagnosis of these tumors is difficult to establish, because symptoms are vague and traditional diagnostic tests are not specific. GISTs shows a wide variety of clinical behavious ranging from benign to frankly malignant, making the outcome totally unpredictable. Surgery is the standard treatment of local GIST while Imatinib (tyrosine kinasi inhibitor) is considered as the standard treatment of metastatic disease.


Resistence to Imatinib is also becoming a major clinical problem but new tirosyne kinase inibitor are being studing to improve the treatment and survival. The present paper is a review of the salient features of epidemiology, pathophysiology, diagnosis, therapy and prognostic factors of GIST.

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How to Cite
Ridolfini, Marco Pericoli, et al. “Gastrointestinal Stromal Tumors”. Annali Italiani Di Chirurgia, vol. 82, no. 2, Mar. 2011, pp. 97-109, https://annaliitalianidichirurgia.it/index.php/aic/article/view/1057.
Section
Review