Two patients with acquired hemophilia successfully treated with combination therapy including therapeutic plasmapheresis / 대한내과학회지
Korean Journal of Medicine
;
: 367-370, 2009.
Artigo
em Inglês
| WPRIM
| ID: wpr-150700
ABSTRACT
Acquired hemophilia is a rare disorder associated with fatal bleeding caused by the development of autoantibodies against factor VIII. Here, we report the cases of two young women with acquired hemophilia who presented with massive internal hemorrhage and purpura. Both patients were successfully treated with combination therapy including factor VIII or factor VIII bypassing agent, immunosuppressants, and therapeutic plasmapheresis.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Púrpura
/
Autoanticorpos
/
Fator VIII
/
Plasmaferese
/
Hemofilia A
/
Hemorragia
/
Imunossupressores
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
Korean Journal of Medicine
Ano de publicação:
2009
Tipo de documento:
Artigo
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