Your browser doesn't support javascript.
loading
Giant metastatic mixed-type spinal ependymoma presenting with hydrocephalus.
Benomar, Anass; Khellaf, Abdelhakim; Kadi, Lynda; Ferreira, José; Lavergne, Pascal; Bergeron, François; Laroche, Mathieu.
Afiliación
  • Benomar A; Department of Radiology, Radiation Oncology and Nuclear Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montréal, Quebec, Canada.
  • Khellaf A; Department of Anatomical Pathology, Centre Hospitalier de l'Université de Montréal (CHUM), Montréal, Quebec, Canada.
  • Kadi L; Department of Radiology, Radiation Oncology and Nuclear Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montréal, Quebec, Canada.
  • Ferreira J; Department of Anatomical Pathology, Maisonneuve-Rosemont Hospital, Montréal, Quebec, Canada.
  • Lavergne P; Division of Neurosurgery, Department of Surgery, Sacré-Coeur Hospital, Montréal, Quebec, Canada.
  • Bergeron F; Department of Radiology, Sacré-Coeur Hospital, Montréal, Quebec, Canada.
  • Laroche M; Division of Neurosurgery, Department of Surgery, Sacré-Coeur Hospital, Montréal, Quebec, Canada.
Radiol Case Rep ; 19(11): 4751-4754, 2024 Nov.
Article en En | MEDLINE | ID: mdl-39228951
ABSTRACT
Ependymomas are rare nervous system tumors that can arise anywhere in the neuraxis. While having a high propensity for leptomeningeal dissemination, retrograde dissemination (from the spine to the CNS) remains infrequent. We describe the case of a 31-year-old female who presented with hydrocephalus secondary to an intracranial leptomeningeal metastasis of a giant spinal ependymoma with mixed (classic and myxopapillary) histopathologic features, successfully treated with surgical resection and radiotherapy of the entire neuraxis. This case highlights the importance of including ependymomas in the differential diagnosis for lesions in atypical extra-axial locations, of systematically obtaining imaging of the entire neuraxis when suspecting it, and of considering retrograde dissemination when both intracranial and spinal lesions are present.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Radiol Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Radiol Case Rep Año: 2024 Tipo del documento: Article