## Abstract Inflammatory myofibroblastic tumor (IMT) is a neoplasm composed of myofibroblastic spindle cells and infiltrating inflammatory cells. Cytogenetic analyses have revealed that a subgroup of IMT, in particular among children and young adults, harbors clonal chromosomal rearrangements invol
ALK-ATIC fusion in urinary bladder inflammatory myofibroblastic tumor
β Scribed by Maria Debiec-Rychter; Peter Marynen; Anne Hagemeijer; Patrick Pauwels
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 238 KB
- Volume
- 38
- Category
- Article
- ISSN
- 1045-2257
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β¦ Synopsis
Abstract
In this report, we describe an inflammatory myofibroblastic tumor (IMT) of the urinary bladder in a 46βyearβold man. Tumor cells presented striking cytoplasmatic ALK immunopositivity. Cytogenetic and FISH analysis, by use of a multicolor chromosome 2 banding probe, revealed a 46,XY,der(2)(2pterβ2p23:2q35β2q37:2p11β2q35:2p23β2p11:2q37β2qter) karyotype. Subsequent FISH and RTβPCR analysis confirmed the ALKβATIC chimeric fusion in tumor cells. This is the first evidence of a variant rearrangement involving the ATIC gene in IMT and the first cytogenetic description of an IMT originating from the urinary bladder. Β© 2003 WileyβLiss, Inc.
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Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal proliferation of transformed myofibroblasts, with a prominent inflammatory cell component, that can mimic other spindle cell processes such as nodular fasciitis, desmoid tumor, and gastrointestinal stromal tumor. Genetic analyses have re
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