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[A new case report and review of the literature].

Authors
  • Ngo, Carine1
  • Khneisser, Pierre2
  • Kanaan, Christina2
  • Valent, Alexander3
  • Dumont, Sarah4
  • Adam, Julien2
  • Scoazec, Jean-Yves5
  • 1 Service de pathologie morphologique, département de biologie et pathologie médicales, Gustave Roussy Cancer Campus, 114, rue Edouard-Vaillant, 94800 Villejuif, France. Electronic address: [email protected] , (France)
  • 2 Service de pathologie morphologique, département de biologie et pathologie médicales, Gustave Roussy Cancer Campus, 114, rue Edouard-Vaillant, 94800 Villejuif, France. , (France)
  • 3 Service de génétique des tumeurs, laboratoire de cytogénétique, département de biologie et pathologie médicales, Gustave-Roussy Cancer Campus, Villejuif, France. , (France)
  • 4 Département d'oncologie médicale, Gustave Roussy-Cancer Campus, Villejuif, France. , (France)
  • 5 Service de pathologie morphologique, département de biologie et pathologie médicales, Gustave Roussy Cancer Campus, 114, rue Edouard-Vaillant, 94800 Villejuif, France; Faculté de médecine de Bicêtre, université Paris Saclay, Le Kremlin-Bicêtre, France. , (France)
Type
Published Article
Journal
Annales de Pathologie
Publisher
Elsevier
Publication Date
Apr 01, 2021
Volume
41
Issue
2
Pages
207–211
Identifiers
DOI: 10.1016/j.annpat.2020.08.004
PMID: 33077252
Source
Medline
Keywords
Language
French
License
Unknown

Abstract

Sarcoma with EWSR1-PATZ1 gene fusion is an exceedingly rare and newly described Ewing-like sarcoma harboring EWSR1 rearrangements involving fusion partners other than ETS family genes. The clinical, histopathologic and immunophenotypic features of cases reported in literature are fairly diverse and not specific. We report a new case report posing real challenges for histological and molecular diagnosis. Copyright © 2020 Elsevier Masson SAS. All rights reserved.

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