Successful Treatment of Acquired Hemophilia A With Rituximab and Steroids in a 5-Year-Old Girl

摘要: Acquired hemophilia A is a very rare, serious bleeding disorder. We describe 5-year-old female who developed an acquired factor VIII inhibitor, and while under treatment with steroids, had intestinal perforation peritonitis septic shock, making her poor candidate for further immunosuppression. She was treated rituximab rapid, complete eradication of the inhibitor. represents first published case pediatric patient successfully rituximab.