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        "titulo" => "Abstract"
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Beh&#231;et&#39;s disease is an inflammatory systemic disorder&#44; with oral and genital ulcers&#44; as well as ophthalmologic and cutaneous disturbances&#46; Five percent of the patients have neurological alterations&#46; We present a case of neuroBeh&#231;et with a rare neurological involvement&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A 28-years-old male patient with recurrent oral and genital ulcer history and folliculitis presents 48 h progressive fever&#44; headache&#44; nausea&#44; right sixth cranial nerve palsy&#44; and right upper limb paresis&#46; The CSF showed lymphocyte pleocytosis and high proteinorrachia&#44; so antibiotic treatment was initiated&#46; Cerebral MR found hyperintense enhancing lesions in the brainstem and left transverse sinus thrombosis&#46; Patient improved with endovenous corticosteroids and was discharged asymptomatic&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Neurological involvement in Beh&#231;et&#39;s disease is rare and moreover the coexistence of parenchymatous and non-parenchymatous alterations in the same patient&#46; It normally has a good response to immunosuppressant treatment&#46;</p>"
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        "resumen" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">La enfermedad de Beh&#231;et es un trastorno inflamatorio sist&#233;mico&#44; caracterizado por aftosis orogenital as&#237; como por alteraciones oftalmol&#243;gicas y cut&#225;neas&#46; Un 5&#37; de los pacientes presenta manifestaciones neurol&#243;gicas&#46; Se presenta un caso de neurobeh&#231;et con participaci&#243;n neurol&#243;gica inhabitual&#46;</p><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Var&#243;n de 28 a&#241;os con antecedente de aftas orales y genitales recurrentes e historia de foliculitis&#44; que acudi&#243; por cuadro de 48 h de fiebre&#44; cefalea&#44; n&#225;useas&#44; paresia del sexto par craneal y del miembro superior derecho&#46; El an&#225;lisis del l&#237;quido cefalorraqu&#237;deo revel&#243; pleocitosis linfocitaria con hiperproteinorraquia&#44; se inici&#243; tratamiento antibi&#243;tico de amplio espectro&#46; Se realiz&#243; resonancia magn&#233;tica cerebral&#44; que mostr&#243; lesiones hiperintensas de predominio troncoencef&#225;lico con realce tras infusi&#243;n de gadolinio y trombosis del seno transverso izquierdo&#46; El paciente mejor&#243; progresivamente con tratamiento intravenoso con corticoides hasta quedar asintom&#225;tico&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">La afectaci&#243;n neurol&#243;gica en la enfermedad de Beh&#231;et es infrecuente y m&#225;s a&#250;n la coexistencia de lesiones intraparenquimatosas y extraparenquimatosas&#46; Habitualmente&#44; presenta buena respuesta al tratamiento inmunosupresor&#46;</p>"
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NeuroBehçet: a case
Neurobehçet: a propósito de un caso
Germán Latorre González
Corresponding author
ger.latorre@gmail.com

Corresponding author.
, Ana Belén Escribano Gascón, Carlos López de Silanes de Miguel, Rocío García Cobos, Luis Ignacio Casanova Peño, Teresa Lapeña Montero
Hospital Clínico San Carlos, Madrid, Spain
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Beh&#231;et&#39;s disease is an inflammatory systemic disorder&#44; with oral and genital ulcers&#44; as well as ophthalmologic and cutaneous disturbances&#46; Five percent of the patients have neurological alterations&#46; We present a case of neuroBeh&#231;et with a rare neurological involvement&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A 28-years-old male patient with recurrent oral and genital ulcer history and folliculitis presents 48 h progressive fever&#44; headache&#44; nausea&#44; right sixth cranial nerve palsy&#44; and right upper limb paresis&#46; The CSF showed lymphocyte pleocytosis and high proteinorrachia&#44; so antibiotic treatment was initiated&#46; Cerebral MR found hyperintense enhancing lesions in the brainstem and left transverse sinus thrombosis&#46; Patient improved with endovenous corticosteroids and was discharged asymptomatic&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Neurological involvement in Beh&#231;et&#39;s disease is rare and moreover the coexistence of parenchymatous and non-parenchymatous alterations in the same patient&#46; It normally has a good response to immunosuppressant treatment&#46;</p>"
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