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[Gastrointestinal stromal tumors]

Authors :
Ridolfini, Mp
Cassano, Alessandra
Ricci, Roberta
Rotondi, Fabio
Berardi, Silvia
Cusumano, Giacomo
Pacelli, Fabio
Doglietto, Giovanni
Cassano, Alessandra (ORCID:0000-0002-3311-7163)
Pacelli, Fabio (ORCID:0000-0002-2013-6525)
Doglietto, Giovanni (ORCID:0000-0002-7394-768X)
Ridolfini, Mp
Cassano, Alessandra
Ricci, Roberta
Rotondi, Fabio
Berardi, Silvia
Cusumano, Giacomo
Pacelli, Fabio
Doglietto, Giovanni
Cassano, Alessandra (ORCID:0000-0002-3311-7163)
Pacelli, Fabio (ORCID:0000-0002-2013-6525)
Doglietto, Giovanni (ORCID:0000-0002-7394-768X)
Publication Year :
2011

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 fom 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 behaviours ranging fom 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 studied 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

Details

Database :
OAIster
Notes :
Italian
Publication Type :
Electronic Resource
Accession number :
edsoai.on1105001062
Document Type :
Electronic Resource