Diffuse leptomeningeal involvement by a ganglioglioma in a child
- 1 August 1992
- journal article
- case report
- Published by Journal of Neurosurgery Publishing Group (JNSPG) in Journal of Neurosurgery
- Vol. 77 (2) , 302-306
- https://doi.org/10.3171/jns.1992.77.2.0302
Abstract
Gangliogliomas are tumors composed of neuronal and glial elements that typically grow slowly by expansion only. This report describes a 20-month-old girl with a ganglioglioma that extensively involved the subarachnoid space; microscopic foci of tumor were found in the brain and spinal cord. Despite chemotherapy and radiation therapy, the child died 5 months after diagnosis. Molecular genetic analysis showed loss of chromosome 17p DNA sequences in the tumor tissue.Keywords
This publication has 17 references indexed in Scilit:
- Deletion mapping of the medulloblastoma locus on chromosome 17pGenomics, 1990
- A genetic model for colorectal tumorigenesisCell, 1990
- Dysembryoplastic neuroepithelial tumorNeurosurgery, 1988
- Leptomeningeal spread of intramedullary spinal cord tumorsJournal of Neurosurgery, 1988
- Ganglioglioma: A Correlative Clinicopathological and Radiological Study of Ten Surgically Treated Cases with Follow-UpNeurosurgery, 1987
- Anaplastic Ganglioglioma in an Infant: Case Report and Review of the LiteratureNeurosurgery, 1986
- Intracerebral gangliogliomaJournal of Neurosurgery, 1986
- Gangliogliomas: pathological and clinical correlationJournal of Neurosurgery, 1981
- Gangliogliomas in ChildrenPediatric Neurosurgery, 1978
- GANGLIOGLIOMAArchives of Neurology & Psychiatry, 1930