Dogan, Ebru ApaydinOzturk, Banu TurgutMutluer, MuzafferYildiz, Gulce UnalGenc, EmineYuruten, BetigulKocaogullar, Yalcin2020-03-262020-03-2620110967-5868https://dx.doi.org/10.1016/j.jocn.2010.05.027https://hdl.handle.net/20.500.12395/26624A 21-year-old male presented with severe throbbing headache, nausea, vomiting and progressive visual loss. Clinical examination revealed bilateral papilledema and left abducens nerve palsy. MRI showed findings consistent with ducal sinus thrombosis. Combinging the clinical findings, MRI and a positive pathergy test, the patient was diagnosed with dural sinus thrombosis associated with Behcet's disease (BD). Despite acetazolamide, prednisone, azathioprine and repeated lumbar punctures, his signs and symptoms of intracranial hypertension gradually worsened. Therefore, lumboperitoneal shunting was planned after which rapid resolution of intracranial hypertension was observed. After reviewing similar reports, we suggest that lumboperitoneal shunt placement can be an effective treatment for patients with BD with medically refractory intracranial hypertension associated with dural sinus thrombosis. (C) 2010 Elsevier Ltd. All rights reserved.en10.1016/j.jocn.2010.05.027info:eu-repo/semantics/closedAccessBehcet's diseaseIntracranial hypertensionLumboperitoneal shuntPapilledemaLumboperitoneal shunt in a patient with Behcet's disease with medically refractory intracranial hypertensionArticle18340941121237657Q2WOS:000287636500026Q4