Malignant rhabdoid tumour of the pineal region

Can J Neurol Sci. 1994 Aug;21(3):273-7. doi: 10.1017/s0317167100041287.

Abstract

A 9-month-old male presented to hospital with signs and symptoms of raised intracranial pressure. A CT scan showed obstructive hydrocephalus from a large pineal region mass lesion into which an intratumoral hemorrhage had occurred. A posterior fossa craniectomy and subtotal excision of the mass lesion were performed. By histopathology, the lesion was a malignant rhabdoid tumour (MRT). Despite surgery and chemotherapy, the tumour grew inexorably, and the patient died four months after the initial diagnosis. MRT is a rare and highly invasive neoplasm which infrequently arises from the central nervous system. This is the first documented case of a MRT arising from the pineal region. The clinical, radiographic, and pathological features of the MRT in this patient are presented.

Publication types

  • Case Reports

MeSH terms

  • Brain Neoplasms / complications
  • Brain Neoplasms / diagnostic imaging
  • Brain Neoplasms / pathology*
  • Brain Neoplasms / ultrastructure
  • Cerebral Hemorrhage / etiology
  • Cerebral Hemorrhage / pathology
  • Fatal Outcome
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Microscopy, Electron
  • Pineal Gland / diagnostic imaging
  • Pineal Gland / pathology*
  • Pineal Gland / ultrastructure
  • Radiography
  • Rhabdoid Tumor / complications
  • Rhabdoid Tumor / diagnostic imaging
  • Rhabdoid Tumor / pathology*
  • Rhabdoid Tumor / ultrastructure