Volume 51, Issue 4 pp. 545-548
Brief Report

Intracerebral small round cell tumor: An unusual case with EWS-WT1 translocation

Karim Bouchireb MD

Karim Bouchireb MD

Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, Villejuif, France

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Nathalie Auger PhD

Nathalie Auger PhD

Department of Clinical Biology, Institut Gustave Roussy, Villejuif, France

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Ranjeev Bhangoo MD

Ranjeev Bhangoo MD

University Paris Sud, UPRES EA3535 “Pharmacology and new treatments of cancer”, Institut Gustave Roussy, Villejuif, France

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Federico Di Rocco MD

Federico Di Rocco MD

Department of Neurosurgery, Hopital Necker, Paris, France

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Nicole Brousse MD

Nicole Brousse MD

Centre de Ressources Biologiques, Département d'Anatomie Pathologique, Hôpital Necker—Enfants Malades, Paris, France

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Olivier Delattre PhD

Olivier Delattre PhD

Laboratoire de pathologie moléculaire des cancers, Institut Curie, Paris, France

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Pascale Varlet MD

Pascale Varlet MD

Laboratoire de Neuropathologie, Centre Hospitalier Sainte Anne, Paris, France

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Jacques Grill MD, PhD

Corresponding Author

Jacques Grill MD, PhD

University Paris Sud, UPRES EA3535 “Pharmacology and new treatments of cancer”, Institut Gustave Roussy, Villejuif, France

Institut Gustave Roussy-Pediatric and Adolescent Oncology 39, rue Camille Desmoulins Villejuif 94805, France.===Search for more papers by this author
First published: 16 June 2008
Citations: 13

Abstract

Desmoplastic small round cell tumor (DSRCT) is a rare tumor, seen both in children and young adults with a marked predilection for the peritoneal cavity. Histology showed a small round cell tumor with a fibromyxoïd stroma and immunohistochemistry indicated neural and mesenchymal differentiation, and diagnosis was made by molecular detection of the EWS-WT1 fusion gene product. DSRCT should be considered in the differential diagnosis of intracranial small round cell tumors. Pediatr Blood Cancer 2008;51:545–548. © 2008 Wiley-Liss, Inc.

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