Pd. Sawin et al., Spinal cord ganglioglioma in a child with neurofibromatosis Type 2 - Case report and literature review, J NEUROSURG, 90(4), 1999, pp. 231-233
Gangliogliomas of the spinal cord are rare disease entities that occur in e
arly childhood. Their occurrence in association with neurofibromatosis Type
2 (NF2) has not been described. The authors describe the unique case of a
2-year-old child with stigmata of NF2 who harbored a spinal cord gangliogli
oma that presented as a rapidly growing, exophytic intramedullary mass lesi
on at the cervicomedullary junction. Treatment consisted of complete surgic
al resection. Histopathological analysis of the lesion demonstrated a mixed
population of neoplastic cells, of both neuronal and glial lineage, that s
upported the diagnosis of ganglioglioma.