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Imatinib as adjuvant therapy for high risk GIST: a case report
Author(s) -
Patrizia Lista,
Agostino Ponzetti
Publication year - 2015
Publication title -
clinical management issues
Language(s) - English
Resource type - Journals
eISSN - 2283-3137
pISSN - 1973-4832
DOI - 10.7175/cmi.v5i4s.1124
Subject(s) - medicine , gist , imatinib , adjuvant therapy , abdominal mass , pathological , laparotomy , cd117 , surgery , perforation , stromal tumor , adjuvant , gastroenterology , cd34 , oncology , stromal cell , chemotherapy , materials science , stem cell , myeloid leukemia , biology , metallurgy , punching , genetics
We here report a case of 42 years old man who experienced sudden abdominal cramps and then underwent explorative laparotomy because of the CT-finding of a 23 cm abdominal mass at the stomach. Frozen specimen analysis indicated a probable gastrointestinal stromal tumor (GIST). Radical excision was performed. Definitive pathological analysis revealed a CD34 and CD 117(c-KIT) positive GIST with a mitotic count of 15/50 HPF. These features indicate a disease with an high risk of recurrence within few years. Molecular analysis found a WK557-558 deletion of c-KIT exon 11, that indicates a poor prognosis in patients with completely resected GIST. In april 2010 he started adjuvant therapy with imatinib at standard dose of 400 mg/day that was well tolerated: he reported only G1 periocular edema and conjunctivitis. Considering the risk of disease recurrence he continued adjuvant therapy beyond the first year.

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