Gastrointestinal stromal tumor with KIT mutation in neurofibromatosis type 1.
10.4174/jkss.2011.81.4.276
- Author:
Hwan NAMGUNG
1
Author Information
1. Department of Surgery, Dankook University College of Medicine, Cheonan, Korea. gsnamgung@dankook.ac.kr
- Publication Type:Case Report
- Keywords:
Gastrointestinal stromal tumors;
Neurofibromatosis type 1;
KIT;
Mutation
- MeSH:
Actins;
Cytoplasm;
Eosinophils;
Exons;
Female;
Gastrointestinal Stromal Tumors;
Humans;
Middle Aged;
Muscle, Smooth;
Neurofibromatoses;
Neurofibromatosis 1;
Point Mutation
- From:Journal of the Korean Surgical Society
2011;81(4):276-280
- CountryRepublic of Korea
- Language:English
-
Abstract:
Multiple jejunalgastrointestinal stromal tumors (GISTs) were found in a 52-year-old woman with a history of neurofibromatosis type 1. These tumors were composed of interlacing fascicles of uniform spindle cells with eosinophilic cytoplasm. Immunohistochemically, the tumor cells were positive for CD117, CD34 and negative for S-100, smooth muscle actin. Molecular analysis for activating mutations of KIT and PDGFRA was performed in two tumors. Contrary to sporadic GISTs, the NF1-associated GISTs are characterized by rare mutations of KIT or PDGFRA. But, one missense point mutation (Trp557Gly) was identified in KIT exon 11 of the extramural portion of the largest tumor in this case. The intramural portion of the largest tumor and the other tumor had wild type KIT and PDGFRA.
