| Literature DB >> 8000986 |
M Muller1, S L Hubbard, J Provias, M Greenberg, L E Becker, J T Rutka.
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.Entities:
Mesh:
Year: 1994 PMID: 8000986 DOI: 10.1017/s0317167100041287
Source DB: PubMed Journal: Can J Neurol Sci ISSN: 0317-1671 Impact factor: 2.104