Low-grade fibro-myxoid sarcoma of intracranial origin: A case report and literature review.

Authors

  • José L. León-Palacios
  • Augusto M. Palacios M
  • Sandro Casavilca-Zambrano
  • Darío Darío Esteban-Arias
  • Sandro E. Sánchez A
  • Wesley Alaba G
  • Ronald A. Pineda G

DOI:

https://doi.org/10.20453/rnp.v83i3.3800

Abstract

Low-grade fibromyxoid sarcoma (LGFMS) is a soft tissue tumor of mesenchymal origin. Sarcomas are a heterogeneous group, representing 1% of all neoplasm diagnoses. Primary sarcomas of the central nervous system (CNS) are rare, and represent only 0.7% of all sarcomas, with an estimated incidence of 3 per 10 million people per year. The case of a 59-year-old woman who developed a low-grade intracranial fibromyxoid sarcoma in the right parietal region, is described. The clinical course, imaging studies, histopathological features, and treatment approach of this unusual diagnosis, are discussed. Low-grade intracranial fibromyxoid sarcoma is a rare and probably under- reported condition. The definitive diagnosis is usually made through histo-pathological studies.

Published

2020-10-09

How to Cite

1.
León-Palacios JL, Palacios M AM, Casavilca-Zambrano S, Darío Esteban-Arias D, Sánchez A SE, Alaba G W, et al. Low-grade fibro-myxoid sarcoma of intracranial origin: A case report and literature review. Rev Neuropsiquiatr [Internet]. 2020 Oct. 9 [cited 2024 Jul. 3];83(3):203-7. Available from: https://revistas.upch.edu.pe/index.php/RNP/article/view/3800

Most read articles by the same author(s)