Otro
Mixed germ cell tumor of the pituitary-hypothalamic region presenting as craniopharyngioma: Case report and review of the literature
Registro en:
Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 9, p. 1501-1504, 2008.
0004-2730
1677-9487
10.1590/S0004-27302008000900015
S0004-27302008000900015
2-s2.0-60149112102.pdf
2-s2.0-60149112102
Autor
Chang, Claudia Veiga
Nunes, Vânia dos Santos
Felicio, Andre Carvalho
Zanini, Marco Antonio
Cunha-Neto, Malebranche B. C.
De Castro, Ana Valeria Barros
Resumen
Craniopharyngiomas and germ cell tumors (GCT) may affect the pituitary-hypothalamic region during childhood. Although different in origin, their clinical and radiological features may be similar. In this article we present a 5-year-old girl with clinical and radiological findings (computer tomography calcification) that were initially considered as craniopharyngioma. However clinical outcome, blood and cerebral spinal fluid tumoral markers, and results from anatomopathology and immunohistochemistry disclosed a mixed GCT. This case report highlights that some clinical features and radiological findings of pituitary-hypothalamic tumors may be misdiagnosed as craniopharyngioma mainly when there is a mature teratoma with cartilaginous tissue differentiation. Copyright© ABE&M.