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Intracranial falx chondroma: Literature review and a case report

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Auteur
Fountas, K. N.; Stamatiou, S.; Barbanis, S.; Kourtopoulos, H.
Date
2008
DOI
10.1016/j.clineuro.2007.08.020
Sujet
chondroma
falx
histopathology
imaging characteristics
outcome
surgical extirpation
OF-THE-LITERATURE
CYSTIC FALCINE CHONDROMA
SOLITARY CHONDROMA
GIANT
CHONDROMA
MESENCHYMAL CHONDROSARCOMA
DURAL CHONDROMA
CHOROID-PLEXUS
CONVEXITY
TUMORS
ENCHONDROMA
Clinical Neurology
Surgery
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Résumé
Intracranial chondromas are benign tumors that represent approximately 0.5% of all intracranial tumors. They usually occur at the base of the skull but on rare occasions might present as intra-parenchymal or intra-ventricular space-occupying lesions, most likely originating from heterotopic chondrocytes or metaplastic fibroblasts of the falx, the convexity dura, or the ventricular ependyma. Chondromas are slow-growing tumors, which remain clinically silent for a prolonged period of time in the majority of cases. Their clinical presentation is non-specific and their radiographic appearance usually does not differentiate them from their more common counterparts, such as meningiomas and glial tumors. As a result, their diagnosis has remained a histopathologic one. In our current study, we present a case of a falcine intracranial chondroma. This case provided the opportunity to extensively review the pertinent literature. (c) 2007 Elsevier B.V. All rights reserved.
URI
http://hdl.handle.net/11615/27534
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