Successful treatment with rituximab in a patient with TTP secondary to severe ANCA-associated vasculitis

18Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

We report a case of thrombotic thrombocytopenic purpura (TTP) secondary to antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis treated by rituximab. TTP secondary to ANCA-associated vasculitis is very rare and has a high mortality rate. We employed rituximab and successfully treated TTP secondary to ANCA-associated vasculitis, because standard therapies, such as steroid therapy, intravenous pulse cyclophosphamide, and repeated plasma exchange (PE), did not suppress her disease activity. This is the first report to suggest that rituximab can achieve complete remission of TTP secondary to ANCA-associated vasculitis. © 2010 The Japanese Society of Internal Medicine.

Cite

CITATION STYLE

APA

Asamiya, Y., Moriyama, T., Takano, M., Iwasaki, C., Kimura, K., Ando, Y., … Nitta, K. (2010). Successful treatment with rituximab in a patient with TTP secondary to severe ANCA-associated vasculitis. Internal Medicine, 49(15), 1587–1591. https://doi.org/10.2169/internalmedicine.49.3135

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free