| Literature DB >> 19777285 |
Tobien Schreuder1, Merijn Te Lintelo, Bela Kubat, Peter Koehler.
Abstract
We report a 71-year-old woman who presented with a cerebral cavernous malformation in the right frontal lobe for which she underwent total resection. Three years later, she was admitted with seizures and neuroimaging revealed a partially calcified lesion in the area of the earlier cavernous malformation, consistent with a residual malformation. A few months later she presented with cognitive decline and neuroimaging now revealed a large mass lesion in the same area as the cavernous malformation, irregularly enhancing, spreading through the corpus callosum to the left frontal lobe. Histological examination showed an anaplastic oligo-astrocytoma. These findings suggest that cerebral cavernous malformations, or at least a subgroup, have the potential for oligodendrocytic and astrocytic transformation. Various hypotheses to explain the etiology of these rare cases are discussed.Entities:
Mesh:
Year: 2009 PMID: 19777285 DOI: 10.1007/s00415-009-5322-0
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849