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Evolución benigna de un glioblastoma multiforme hipotalámico. Caso clínico
M. Clavel Escribano, B. López Ibor, P. Clavel Laria
Servicios de Neurocirugía y Oncología Pediátrica del Hospital General de Cataluña. Barcelona
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">We are reporting the case of a two years old girl with a clinical history of sudden onset of increased intracranial pressure&#46; The neuroimaging studies disclosed a large hypothalamic mass &#40;glioblastoma multiforme&#41; extending to the third ventricle and the floor of the lateral ventricles&#44; causing hydrocephalus by the obstruction of Monro foramina&#46; The tumor was subtotalIy resected through a subfrontal bilateral microsurgical approach&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">After surgery she was treated with several cycles of chemotherapy&#46; The only rest of the tumor&#44; left at the level of the optic chiasm&#44; disappeared in the last MRI control&#46; Three years after surgery the patient is asymptomatic and tumor-free&#46;</p>"
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