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Epithelioid and spindle cell rhabdomyosarcoma with EWSR1::TFCP2 fusion mimicking metastatic lung cancer: A case report and literature review.
Haug, Lukas; Doll, Julia; Appenzeller, Silke; Kunzmann, Volker; Rosenwald, Andreas; Maurus, Katja; Gerhard-Hartmann, Elena.
Afiliación
  • Haug L; Institute of Pathology, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany.
  • Doll J; Institute of Pathology, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany.
  • Appenzeller S; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany.
  • Kunzmann V; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Rosenwald A; Institute of Pathology, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany.
  • Maurus K; Institute of Pathology, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany.
  • Gerhard-Hartmann E; Institute of Pathology, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University Hospital of Würzburg, Würzburg, Germany. Electronic address: Elena.Hartmann@uni-wuerzburg.de.
Pathol Res Pract ; 249: 154779, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37633005
Rhabdomyosarcoma (RMS) with EWSR1/FUS::TFCP2 fusion is an emerging, molecularly defined, rare subtype of RMS. It can affect patients in a wide age range and follows an aggressive clinical course according to the reported cases. Due to its unusual clinical and pathohistological features, with a typical intraosseous presentation and common cytokeratin expression, the diagnosis is challenging, and metastatic undifferentiated/sarcomatoid carcinoma can be an important differential diagnosis. We report here a case of a 55-year-old woman with an RMS with EWSR1::TFCP2 fusion mimicking metastatic lung cancer in view of the clinical and microscopic presentation. However, further molecular workup, including RNA sequencing, led to the proper diagnosis. Although these tumors are rare, knowledge of their unique features is essential for correct diagnosis as a basis for clinical management and optimization of therapeutic approaches.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Carcinoma / Rabdomiosarcoma Embrionario / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Female / Humans / Middle aged Idioma: En Revista: Pathol Res Pract Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Carcinoma / Rabdomiosarcoma Embrionario / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Female / Humans / Middle aged Idioma: En Revista: Pathol Res Pract Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Alemania