Background Idiopathic intracranial hypertension is a rare disorder, characterized by raised intracranial pressure with no recognizable cause. Headache, decreased visual acuity and papilledema are the main clinical manifestations. Case description A case of a 27-year-old obese woman affected by idiopathic intracranial hypertension is reported. She was initially treated conservatively, but, due to severe headache refractory to medical therapy, an adjustable lumbo-peritoneal shunt was implanted. Conclusion Gold standard treatment of idiopathic intracranial hypertension is not defined yet, but the lumbo-peritoneal shunt could represent a valid option for managing the disease in properly selected patients.

Is the adjustable lumbo-peritoneal shunt a valid option for managing symptomatic idiopathic intracranial hypertension? A case report of a multidisciplinary management / U.A. Arcidiacono, P.P. Vico, F. Pessina, M. Riva. - In: INTERDISCIPLINARY NEUROSURGERY. - ISSN 2214-7519. - 18(2019). [10.1016/j.inat.2019.100484]

Is the adjustable lumbo-peritoneal shunt a valid option for managing symptomatic idiopathic intracranial hypertension? A case report of a multidisciplinary management

M. Riva
Ultimo
2019

Abstract

Background Idiopathic intracranial hypertension is a rare disorder, characterized by raised intracranial pressure with no recognizable cause. Headache, decreased visual acuity and papilledema are the main clinical manifestations. Case description A case of a 27-year-old obese woman affected by idiopathic intracranial hypertension is reported. She was initially treated conservatively, but, due to severe headache refractory to medical therapy, an adjustable lumbo-peritoneal shunt was implanted. Conclusion Gold standard treatment of idiopathic intracranial hypertension is not defined yet, but the lumbo-peritoneal shunt could represent a valid option for managing the disease in properly selected patients.
Lumbo-peritoneal shuntIdiopathic intracranial hypertensionPseudotumor cerebri
Settore MED/27 - Neurochirurgia
2019
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/646172
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