Two patients with acquired hemophilia successfully treated with combination therapy including therapeutic plasmapheresis / 대한내과학회지
Korean Journal of Medicine
; : 367-370, 2009.
Article
in English
| WPRIM (Western Pacific)
| ID: wpr-150700
Responsible library:
WPRO
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.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Purpura
/
Autoantibodies
/
Factor VIII
/
Plasmapheresis
/
Hemophilia A
/
Hemorrhage
/
Immunosuppressive Agents
Limits:
Female
/
Humans
Language:
English
Journal:
Korean Journal of Medicine
Year:
2009
Document type:
Article