SOLITARY FIBROUS TUMOR/HEMANGIOPERICYTOMA (SFT/HPC); A CASE REPORT IN A 15 YEARS OLD PATIENT AND REVIEW OF THE LITERATURE

Autores/as

  • María Gabriela Sánchez Páez General Doctor, Neurological Surgery Service FOSCAL Clinic, Floridablanca Colombia.
  • Johann Serrato Hospital Militar Central - Universidad Militar Nueva Granada
  • Andreina Martínez Amado Medical Student, Nueva Granada Military University, Bogotá, Colombia.
  • Leonardo Chacon 4Neurosurgeon, Neurological Surgery, Central Military Hospital, Nueva Granada Military University, Bogotá, Colombia.
  • Neftali Cossio Neurosurgeon, Neurological Surgery Service FOSCAL Clinic, Floridablanca Colombia.

DOI:

https://doi.org/10.51437/nj.v26i1.143

Palabras clave:

tumor fibroso solitario, hemangiopericitoma, tumores, sistema nervioso central, pericitos.

Resumen

Los tumores fibrosos solitarios / hemangiopericitomas son tumores del sistema nervioso central que a lo largo de los años han sido estudiados, tienen hallazgos y comportamientos similares a los meningiomas, lo que nos presenta un gran desafío al definir un diagnóstico y un tratamiento médico o quirúrgico. Tienen una baja incidencia y su clasificación es estricta según su grado de celularidad y compromiso vascular. La presentación es inusual en los jóvenes, la mayor incidencia es entre la cuarta y sexta década de la vida con predominio en los hombres, en este informe mostramos a un paciente con 15 años de edad que presenta una lesión compatible con un hemangiopericitoma anaplásico o tumor III fibroso solitario / hemangiopericitoma de acuerdo con la clasificación de la OMS a quien se le proporcionó un tratamiento neuroquirúrgico y adyuvante con una resección del 100% de la lesión.

Citas

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Publicado

2020-11-27

Cómo citar

Sanchez Paez , M. G., SERRATO, J., Martinez Amado, A. ., Chacon, L., & Cossio , N. . (2020). SOLITARY FIBROUS TUMOR/HEMANGIOPERICYTOMA (SFT/HPC); A CASE REPORT IN A 15 YEARS OLD PATIENT AND REVIEW OF THE LITERATURE. Neurociencias Journal, 26(1), 100–109. https://doi.org/10.51437/nj.v26i1.143

Número

Sección

Reporte de caso