sindrome de behcet
DESCRIPTION
Sindrome de Behcet - ReumatologiaTRANSCRIPT
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SINDROME DE BEHCET
PROCESO MULTIORGANICO CARACTERIZADO POR .
• ULCERAS EN BOCA Y GENITALES
• COMPROMISO OCULAR
• ETIOLOGIA DESCONOCIDA
• AFECTA ADULTOS JOVENES, MAS GRAVE EN HOMBRES
• PREVALENCIA 1/10.000 EN JAPON, 1/500.000 EN USA, EUROPA
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ANATOMIA PATOLOGICA
• VASCULITIS CON TENDENCIA A LA FORMACION DE TROMBOS VENOSOS
• ANTICUERPOS CIRCULANTES CONTRA MUCOSA BUCAL
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MANIFESTACIONES CLINICAS
• ULCERAS AFTOSAS RESIDIVANTES EN BOCA (SINE QUANON)
• ULCERAS GENITALES
• IRITIS , UVEITIS PUEDEN LLEGAR A CEGUERA
• HIPERREACTIVIDAD INFLAMATORIA DE PIEL.- PATERGIA (INYECCION INTRADERMICA DE SOL. SALINA)
• ARTRITIS DE RODILLAS Y TOBILLOS (N0 EROSIVA)
• HIPERTENSION ENDOCRANEANA
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TRATAMIENTO
• APLICACIÓN LOCAL DE GLUCOCORTICOIDES
• PREDNISONA 1 MGR. KILO PESO DIA PARA COMPROMISO OCULAR
• AZATIOPRINA