[Central nervous system dysgerminoma: a clinicopathological study of 3 cases].

Autor:	Bellil S; Service d'Anatomie et de Cytologie Pathologiques, Hôpital la Rabta., Braham E, Limaiem F, Bellil K, Chelly I, Mekni A, Haouet S, Zitouna M, Jemel H, Khaldi M, Kchir N
Jazyk:	francouzština
Zdroj:	La Tunisie medicale [Tunis Med] 2009 Mar; Vol. 87 (3), pp. 207-9.
Abstrakt:	Background: Intracranial germ cell tumors are rarely seen and typically localize in the pineal or suprasellar region. The largest category of germ cell tumors is dysgerminoma. Aim: to describe clinicopathological features and immunohistochemical profile of dysgerminomas. Case Report: We report three cases of central nervous system dysgerminomas. There were two young women and a man who were 6, 11 and 23-year-old. They presented with symptoms of insipidus diabetes (n=3) with association to visual field defects in the third case. Radiological findings showed a supra seller lesion in two cases. Double localization in the pineal and suprasellar regions was seen in the third case. Histologic examination and immunohistochemical study of surgical specimen were consistent with primary central nervous system dysgerminoma.
Databáze:	MEDLINE
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