Suprasellar chordoid glioma

Citation
Jr. Ricoy et al., Suprasellar chordoid glioma, ACT NEUROP, 99(6), 2000, pp. 699-703
Citations number
8
Categorie Soggetti
Neurosciences & Behavoir
Journal title
ACTA NEUROPATHOLOGICA
ISSN journal
00016322 → ACNP
Volume
99
Issue
6
Year of publication
2000
Pages
699 - 703
Database
ISI
SICI code
0001-6322(200006)99:6<699:SCG>2.0.ZU;2-W
Abstract
Brat et al. (J Neuropathol Exp Neurol 57:288-290, 1998) reported eight case s of a new clinico-pathological entity, which occurs mainly in the third ve ntricle of middle-aged females, which they described as chordoid glioma of the third ventricle. We report a new case of a 41-year-old woman with a sup rasellar chordoid glioma with histological, immunohistochemical and ultrast ructural studies. We discuss the differential diagnosis between chordoma, c hordoid meningioma, germinoma and pituitary adenoma. Histologically, the tu mour showed cords and lobules of isomorphic epithelioid cells in a vacuolat ed matrix with prominent multifocal lymphoplasmacytic infiltrates in which some histiocytes and isolated Touton-type giant cells were seen; cells were immunoreactive for glial fibrillary acidic protein but negative for epithe lial membrane antigen. Ultrastructural examination revealed abundant interm ediate filament but no desmosomes, microvilli nor cilia were seen.