Myxofibrosarcoma: a rare diagnosis

Authors

  • Mariano Ulla-Anes Internal Medicine Service, Hospital Universitario Infanta Leonor, Madrid, Spain
  • Elena Palma-Huertas Internal Medicine Service, Hospital Universitario Infanta Leonor, Madrid, Spain https://orcid.org/0009-0008-7832-6867
  • Manuela Pena-Burgos Anatomical Pathology, Hospital General Universitario Gregorio Marañón, Madrid, Spain
  • Mariano Matarranz-del Amo Internal Medicine, Hospital Universitario Infanta Leonor, Madrid, Spain https://orcid.org/0000-0002-6120-7545
  • Juan Torres-Macho Internal Medicine, Hospital Universitario Infanta Leonor, Madrid, Spain

DOI:

https://doi.org/10.32818/reccmi.a8n2a8

Keywords:

myxofibrosarcoma, malignant mesenchymal tumor, soft-tissue sarcoma

Abstract

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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Published

2023-08-31

How to Cite

1.
Ulla-Anes M, Palma-Huertas E, Pena-Burgos M, Matarranz-del Amo M, Torres-Macho J. Myxofibrosarcoma: a rare diagnosis. Rev Esp Casos Clin Med Intern [Internet]. 2023 Aug. 31 [cited 2024 Dec. 22];8(2):84-7. Available from: https://www.reccmi.com/RECCMI/article/view/869