| Literature DB >> 20951065 |
Hiroaki Miyahara1, Masae Ryufuku, Yong-Juan Fu, Hiroki Kitaura, Hiroatsu Murakami, Hiroshi Masuda, Shigeki Kameyama, Hitoshi Takahashi, Akiyoshi Kakita.
Abstract
The presence of balloon cells, a pathognomonic cellular feature of focal cortical dysplasia type IIB, in a background of hippocampal sclerosis is rare. Here we report the surgical pathologic features of the hippocampus resected from a 32-year-old woman with mesial temporal lobe epilepsy and a precipitating history of non-herpetic acute limbic encephalitis. Histologically, the resected specimen showed features of hippocampal sclerosis with granule cell dispersion. Characteristically, many balloon cells, immunoreactive for nestin, vimentin, glial fibrillary acidic protein (GFAP), GFAP-delta and CD34, were observed in the molecular and granule cell layers of the dentate gyrus. In the present case hippocampal sclerosis was an apparently acquired alteration, rather than a result of maldevelopment. The appearance of balloon cells raises questions regarding their origin and morphogenesis. Copyright ÂEntities:
Mesh:
Year: 2010 PMID: 20951065 DOI: 10.1016/j.seizure.2010.09.013
Source DB: PubMed Journal: Seizure ISSN: 1059-1311 Impact factor: 3.184