RESUMO
A rare case of multiple supratentorial and infratentorial hemangioblastomas in a 50-year old man is presented. There were neither manifestations of visceral tumors nor familial history. The two tumors were totally removed in two sessions and the diagnosis in both tumors were hemangioblastomas.
Assuntos
Humanos , Pessoa de Meia-Idade , Diagnóstico , Hemangioblastoma , Doença de von Hippel-LindauRESUMO
Supratentorial hemangioblastomas are rare and a meningeal location is even rarer. We report a solid meningeal hemangiblastoma in left parietal region, mimicking a meningioma on CT scan. There was no manifestation of von Hippel-Lindau disease. The literature on supratentorial meningeal hemangioblastoma was reviewed.
Assuntos
Hemangioblastoma , Meningioma , Rabeprazol , Tomografia Computadorizada por Raios X , Doença de von Hippel-LindauRESUMO
Supratentorial hemangioblastomas are rare tumors. The first documented case of congenital cystic supratentorial hemangiblastoma associated with intracystic hemorrhage is presented; it occurred in a 38-day-old male infant.