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Am J Transplant ; 9(5): 1223-9, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19422347

RESUMEN

Hemolytic uremic syndrome (HUS) associated with anti-Factor H (anti-FH) autoantibodies is a recently described pathophysiological entity. Monitoring of anti-FH IgG titer may be a sensitive marker of disease activity and guide treatment to eliminate circulating anti-FH antibodies. We report here a case of atypical HUS (aHUS) in which anti-FH autoantibodies were detected during the course of a fifth kidney transplant, 30 years after the first flare of aHUS. This exceptional case suggests that early, specific management based on immunosuppressive therapy and plasma exchanges monitored by anti-FH IgG titer may result in long-term graft survival.


Asunto(s)
Autoanticuerpos/sangre , Factor H de Complemento/inmunología , Síndrome Hemolítico-Urémico/cirugía , Trasplante de Riñón/inmunología , Proteínas Sanguíneas/genética , Niño , Proteínas Inactivadoras del Complemento C3b/genética , Factor B del Complemento/inmunología , Femenino , Eliminación de Gen , Síndrome Hemolítico-Urémico/clasificación , Síndrome Hemolítico-Urémico/inmunología , Humanos , Recurrencia , Reoperación/estadística & datos numéricos
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