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Hurtado-García, C. Trasancos Escura, J.I. Massa Navarrete" "autores" => array:3 [ 0 => array:4 [ "nombre" => "R." "apellidos" => "Hurtado-García" "email" => array:1 [ 0 => "robelx2@gmail.com" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "C." "apellidos" => "Trasancos Escura" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "J.I." 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Cranial tomography showed no acute intracranial hemorrhagic or ischemic lesions. A lumbar puncture showed normal glucose and proteins, with slight lymphocytic pleocytosis. The results of the microbiological study of the cerebrospinal fluid were negative. The ophthalmological examination, which included the eye fundus, was normal.</p><p id="par0015" class="elsevierStylePara elsevierViewall">Magnetic resonance imaging with angiography showed thrombosis with a contrast filling defect in the left sigmoid and transverse sinuses, next to the proximal region of the internal jugular vein (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). There were no other significant abnormalities in the brain parenchyma.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Treatment was initiated with an intravenous bolus of cyclophosphamide<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>250-mg methylprednisolone in a fortnightly regimen. The headaches disappeared within 72<span class="elsevierStyleHsp" style=""></span>h, and the acute phase parameters improved.</p><p id="par0025" class="elsevierStylePara elsevierViewall">Clinical impairment in neuro-Behçet's disease typically presents as acute meningoencephalitis by parenchymal disease due to inflammatory perivasculitis. In other cases, the condition can start with headaches and papilledema associated with dural venous sinus thrombosis. In more uncommon cases, neuro-Behçet's disease can progress with focal neurological defects such as impairment of the pyramidal pathway.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Brain magnetic resonance imaging has a fundamental role in the diagnosis and is the gold standard, enabling the differential diagnosis with other autoimmune diseases.</p></span>" "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2018-05-17" "fechaAceptado" => "2018-06-05" "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Hurtado-García R, Trasancos Escura C, Massa Navarrete JI. Cefalea y enfermedad de Behçet: el enemigo oculto. 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