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Pituicytoma with Significant Tumor Vascularity Mimicking Pituitary Macroadenoma
Brain Tumor Research and Treatment ; : 110-115, 2017.
Artigo em Inglês | WPRIM | ID: wpr-176894
ABSTRACT
A 19-year-old man presented with bitemporal hemianopsia and was found to have a large sellar and suprasellar tumor, resembling a pituitary macroadenoma. Emergency transsphenoidal approach was attempted because of rapid visual deterioration with headache. However, the approach was complicated and stopped by uncontrolled hemorrhage from the tumor. After conventional cerebral angiography and recognition of an unusual pathology, transcranial approach was achieved to prevent permanent visual loss. The final pathological diagnosis was pituicytoma with epithelioid features. Pituicytoma is a rare low-grade tumor (WHO Grade I) of pituicytes involving the sellar and suprasellar region, and originating from special glial cells of the neurohypophysis. Because of the high vascularity, the firm consistency, and invasion to surrounding neurovascular structures, a pituicytoma should be included in the differential diagnosis of a mass in the sellar and suprasellar area if the tumor shows high enhancement with vascular components. We report a case of rare pituicytoma mimicking a pituitary macroadenoma with massive hemorrhage to disturb surgery.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Neuro-Hipófise / Angiografia Cerebral / Hemianopsia / Neuroglia / Diagnóstico / Diagnóstico Diferencial / Emergências / Cefaleia / Hemorragia Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Inglês Revista: Brain Tumor Research and Treatment Ano de publicação: 2017 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Neuro-Hipófise / Angiografia Cerebral / Hemianopsia / Neuroglia / Diagnóstico / Diagnóstico Diferencial / Emergências / Cefaleia / Hemorragia Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Inglês Revista: Brain Tumor Research and Treatment Ano de publicação: 2017 Tipo de documento: Artigo