Inflammatory myofibroblastic tumor with HMGIC rearrangement

被引:22
作者
Kazmierczak, B
Dal Cin, P
Sciot, R
Van den Berghe, H
Bullerdiek, J
机构
[1] Univ Bremen, Ctr Human Genet & Genet Counseling, D-28359 Bremen, Germany
[2] Katholieke Univ Leuven, Ctr Human Genet, Louvain, Belgium
[3] Katholieke Univ Leuven Hosp, Dept Pathol, B-3000 Louvain, Belgium
关键词
D O I
10.1016/S0165-4608(98)00268-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inflammatory pseudotumors or inflammatory myofibroblastic tumors (IMT) are lesions of extreme heterogeneity showing a highly variable mixture of bland-looking spindle cells,inflammatory cells, and collagen fibers. We describe our results of molecular cytogenetic and rapid amplification of cDNA ends (RACE-PCR) studies on an IMT characterized by a translocation involving 12q15. Chromosomal aberrations involving this region are very frequent among other benign tumors such as lipomas, uterine leiomyomas, or pulmonary chondroid hamartomas. Recently, we have shown that, by these structural chromosomal aberrations, the HMGIC gene is affected. Fluorescence in situ hybridization (FISH) analysis and 3' RACE-PCR on cells of the present case of an inflammatory myofibroblastic tumor indicated an intragenic rearrangement of HMGIC, resulting in an aberrant transcript of that gene.. Clonal cytogenetic aberrations have been described in very few cases of IMT. The results presented herein indicate that this case of IMT represents a true benign mesenchymal neoplasm associated with, or due to, a rearrangement of HMGIC. (C) Elsevier Science Inc., 1999. All rights reserved.
引用
收藏
页码:156 / 160
页数:5
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