Intramedullary "holocord" oligodendroglioma: case report.

Abstract:

:Primary spinal cord oligodendrogliomas are rare tumours. Only 3 holocord cases have been reported in the literature. We present a primary intramedullary "holocord" oligodendroglioma in a 13 year-old male. Scoliosis was the initial symptom. Neurological deterioration prompted MRI, which demonstrated the lesion. Total removal was achieved. This case shows that meticulous surgery may obtain an optimal result in holocord oligodendrogliomas. 2 years after surgery, the young patient has made an excellent recovery.

journal_name

Acta Neurochir (Wien)

journal_title

Acta neurochirurgica

authors

Pagni CA,Canavero S,Gaidolfi E

doi

10.1007/BF01402122

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

96-9

issue

1-2

eissn

0001-6268

issn

0942-0940

journal_volume

113

pub_type

杂志文章
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