Abstract
Rhabdoid meningioma are quite rare type of intracranial tumors. according to WHO classification 2016 characterized by high
mitotic index, invasion to healthy brain tissue, high recurrence rate and low survival expectancy, on this occasion we present
the case of a 23 months child diagnosed with this pathology, covering clinical aspects characteristic of the pathology, his pathology of the diagnosis and a short revision of the current literature on the treatment and the survival of these patients.
mitotic index, invasion to healthy brain tissue, high recurrence rate and low survival expectancy, on this occasion we present
the case of a 23 months child diagnosed with this pathology, covering clinical aspects characteristic of the pathology, his pathology of the diagnosis and a short revision of the current literature on the treatment and the survival of these patients.
| Original language | Spanish (Colombia) |
|---|---|
| Article number | 43 |
| Pages (from-to) | 141-145 |
| Number of pages | 4 |
| Journal | Revista chilena de Neurocirugía |
| Volume | 43 |
| State | Published - May 28 2017 |
Cite this
Velandia Hurtado, F. A., Rojas, L. O., Restrepo, C. M., Martinez , A., Mendoza, M. M., & Cuellar, Y. (2017). Meningioma rabdoide Grado III, en paciente pediátrico: Reporte de caso. Revista chilena de Neurocirugía , 43, 141-145. [ 43].