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Artículo en Inglés | IMSEAR | ID: sea-46066

RESUMEN

Behcet's disease (BD) is an autoimmune disease of unknown aetiology with multisystem involvement presenting with relapsing orogenital ulcers and uveitis, involvement of central nervous system, joints, lungs, gastrointestinal tract and major blood vessels leading to myriads of presentations, which requires a multidisciplinary approach for satisfactory outcome. We describe a patient with BD, highlight its pathophysiology and management aspects, and present review of pertinent literature.


Asunto(s)
Adulto , Síndrome de Behçet/diagnóstico , Humanos , Hidrocortisona/uso terapéutico , Masculino , Uveítis/diagnóstico
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