We report a case of infrasellar craniopharyngioma in a 34 year-old woman who presented with progressive headache and diplopia. Computed tomographic and magnetic resonance images showed a heterogeneous tumor originating from the sphenoid bone with ethmoid sinus and sella turcica extension. A sublabial rhinoseptal transsphenoidal surgery was performed. Craniopharyngiomas with infrasellar development are very rare. Infrasellar craniopharyngioma is uncommon, thirty-five cases has been reported in literature. The embryology, clinical features and radiographic investigation of these tumors are discussed.
CITATION STYLE
Falavigna, A., & Kraemer, J. L. (2001). Infrasellar craniopharyngioma: Case report. Arquivos de Neuro-Psiquiatria, 59(2 B), 424–430. https://doi.org/10.1590/S0004-282X2001000300022
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