Turkish Journal of Oncology Turkish Society for Radiation Oncology
Article Open Access Volume 23 · Issue 3 · 2008 pp. 142–146

Ganglioglioma: a case report

Ali Özcan BİNATLI1
1 Tepecik Eğitim ve Araştırma Hastanesi, Nöroşirürji Kliniği, İzmir
2 Tepecik Eğitim ve Araştırma Hastanesi, Patoloji Bölümü, İzmir
3 Ege Üniversitesi Tıp Fakültesi, Nöroşirürji Anabilim Dalı, İzmir
Published: 2008 Pubmed: 77571 Article ID: 701
Abstract
Gangliogliomas are mixed neuronal-glial type tumors of the
central nervous system (CNS). Gangliogliomas are rare
tumors that present histological features and biological
behavior of low-grade malignancy. Gangliogliomas account
for about 0.5% of all CNS tumors, and they generally occur
in childhood. Gangliogliomas make up about 8.0% of CNS
tumors in children. These tumors are mostly localized in the
supratentorial region and often present with seizures. Surgery
is the first choice of treatment. We present a case of a 14-yearold
male who presented with headache, with vomiting added
recently. A left temporal mass was detected during investigations.
The mass was totally resected surgically. The pathology
was reported as ganglioglioma. The patient is being followed
sufficiently in our clinic.

Keywords: Surgery; ganglioglioma; radiotherapy

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