Detection of the EWS/WT1 gene fusion by reverse transcriptase-polymerase chain reaction in the diagnosis of intra-abdominal desmoplastic small round cell tumor.

Abstract

We report two cases of intra-abdominal desmoplastic small round cell tumor with characteristic clinical, histological, immunohistochemical, and ultrastructural features. Fusion of the EWS gene on chromosome 22 and the WT1 gene on chromosome 11, resulting from the chromosomal translocation t(11;22)(p13;q12), was detected by reverse transcriptase polymerase chain reaction (RT-PCR) in both cases. This translocation has been previously reported in this type of tumor using either cytogenetic or molecular biological techniques. Tumor tissue from both cases revealed no chimeric fusion transcripts characteristic of the Ewing sarcoma family of peripheral primitive neuroectodermal tumors or of alveolar rhabdomyosarcoma, two tumors in the differential diagnosis of intra-abdominal desmoplastic small round cell tumor. This report demonstrates the utility of molecular studies as an adjunct in the diagnosis of this rare and aggressive tumor.

• Authors: L H Argatoff, J X O'Connell, J A Mathers, C B Gilks, P H Sorensen
• Journal: The American journal of surgical pathology (Am J Surg Pathol) Vol. 20 Issue 4 Pg. 406-12 (Apr 1996) ISSN: 0147-5185 [Print] United States
• PMID: 8604806 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Abdominal Neoplasms (diagnosis, genetics, pathology)
• Adult
• Genes, Wilms Tumor
• Humans
• Male
• Oncogenes
• Polymerase Chain Reaction
• Sarcoma, Ewing (genetics)
• Sarcoma, Small Cell (diagnosis, genetics, pathology)
• Translocation, Genetic