Inflammatory myofibroblastic tumor with HMGIC rearrangement

Citation
B. Kazmierczak et al., Inflammatory myofibroblastic tumor with HMGIC rearrangement, CANC GENET, 112(2), 1999, pp. 156-160
Citations number
22
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER GENETICS AND CYTOGENETICS
ISSN journal
01654608 → ACNP
Volume
112
Issue
2
Year of publication
1999
Pages
156 - 160
Database
ISI
SICI code
0165-4608(19990715)112:2<156:IMTWHR>2.0.ZU;2-4
Abstract
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 12q 15. Chromosomal aberrations involving this region are very frequent among o ther benign tumors such as lipomas, uterine leiomyomas, or pulmonary chondr oid hamartomas. Recently, we have shown that, by these structural chromosom al aberrations, the HMGIC gene is affected. Fluorescence in situ hybridizat ion (FISH) analysis and 3' RACE-PCR on cells of the present case of an infl ammatory myofibroblastic tumor indicated an intragenic rearrangement of HMG IC, resulting in an aberrant transcript of that gene.. Clonal cytogenetic a berrations have been described in very few cases of IMT. The results presen ted herein indicate that this case of IMT represents a true benign mesenchy mal neoplasm associated with, or due to, a rearrangement of HMGIC. (C) Else vier Science Inc., 1999. All rights reserved.