Mixofibrosarcoma:un diagnóstico infrecuente

  1. Ulla-Anes, Mariano 1
  2. Palma-Huertas, Elena 1
  3. Pena-Burgos, Manuela 2
  4. Matarranz-del Amo, Mariano 1
  5. Torres-Macho, Juan 1
  1. 1 Servicio de Medicina Interna, Hospital Universitario Infanta Leonor, Madrid, España
  2. 2 Servicio de Anatomía Patológica, Hospital General Universitario Gregorio Marañón, Madrid, España
Aldizkaria:
Revista Española de Casos Clínicos en Medicina Interna (RECCMI)

ISSN: 2530-0792

Argitalpen urtea: 2023

Zenbakien izenburua: Revista Española de Casos Clínicos en Medicina Interna

Alea: 8

Zenbakia: 2

Orrialdeak: 84-87

Mota: Artikulua

DOI: 10.32818/RECCMI.A8N2A8 DIALNET GOOGLE SCHOLAR lock_openSarbide irekia editor

Beste argitalpen batzuk: Revista Española de Casos Clínicos en Medicina Interna (RECCMI)

Garapen Iraunkorreko Helburuak

Laburpena

Myxofibrosarcoma is a mesenchymal tumor typical of elderly patients and it has an infiltrative pattern mainly at local level, which fundamentally requires adequate characterization by nuclear magnetic resonance (MRI) and core needle biopsy (CNB), as well as a multidisciplinary team for its treatment. We present the case of an 85-year-old patient with a painless mass on the right thigh who was admitted to the Internal Medicine unit for initial treatment of a condensing respiratory infection. Finally, after an extensive study, she was diagnosed with myxofibrosarcoma.

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