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CC BY-NC-ND 4.0 · Asian J Neurosurg 2021; 16(03): 626-629
DOI: 10.4103/ajns.AJNS_514_20
Case Report

Cranial and spinal oligodendrogliomatosis: A case report and review of the literature

Koral Erdogan
Department of Neurosurgery, Ankara University School of Medicine, Ibn-i Sina Hospital, Ankara
,
Orkhan Mammadkhanli
1   Department of Neurosurgery, Faculty of Medicine, Yuksek Ihtisas University, Ankara
,
Ihsan Dogan
Department of Neurosurgery, Ankara University School of Medicine, Ibn-i Sina Hospital, Ankara
,
Cevriye Ersoz
2   Department of Pathology, Ankara University School of Medicine, Ankara
,
Aylin Okcu
2   Department of Pathology, Ankara University School of Medicine, Ankara
,
Mustafa Unlu
Department of Neurosurgery, Ankara University School of Medicine, Ibn-i Sina Hospital, Ankara
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Secondary leptomeningeal gliomatosis is a condition known as a result of invasion of the subarachnoid space or the ventricular system of primary intraparenchymal glioma. In this article, we present a 7-year-old boy presented with neck and back deformity and deterioration of gait. Cranial and spinal magnetic resonance imaging revealed lesions in the supratentorial and infratentorial areas, in the brainstem downward the spinal cord. Disseminated oligodendrogliomatosis is extremely rare and our case we present is the 24th in the literature.

Key-words:

1p19q deletion - leptomeningeal dissemination - oligodendrogliomatosis

Financial support and sponsorship

Nil.




Publikationsverlauf

Eingereicht: 28. November 2020

Angenommen: 15. April 2021

Artikel online veröffentlicht:
16. August 2022

© 2021. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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