CC BY-NC-ND 4.0 · Asian J Neurosurg 2014; 9(04): 246
DOI: 10.4103/1793-5482.146666
CASE REPORT

L'hermitte-Duclos disease in an elderly patient: A case report and review of the literature

Ersin Ozeren
Department of Neurosurgery, Diskapi Training and Research Hospital, Duzce
,
Levent Gurses
Department of Neurosurgery, Diskapi Training and Research Hospital, Duzce
,
Mehmet Sorar
Department of Neurosurgery, Diskapi Training and Research Hospital, Duzce
,
Uygur Er
1   Department of Neurosurgery, Medical School, Duzce University, Duzce
,
Evrim Önder
Department of Neurosurgery, Diskapi Training and Research Hospital, Duzce
,
Ata Arikök
Department of Neurosurgery, Diskapi Training and Research Hospital, Duzce
› Author Affiliations

L'hermitte-Duclos disease (LDD) is an extremely rare cerebellar lesion of uncertain etiology. Occasionally, the patients with LDD may even have sudden neurological deterioration due to acute heniation as seen in the present case report. It is also imperative to distinguish this disease from other malignant lesion of the cerebellum and cerebellar malformations with its varied natural course of history and hence better ability to prognosticate such patients. Herein, we reported a successfully treated case of LDD following a long history of vaguely defined neurological complaints in an elderly patient and reviewed the literature.



Publication History

Article published online:
22 September 2022

© 2014. 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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