| Literature DB >> 11725831 |
Y Nishino1, K Ueki, M Suto, H Uchiumi, F Ota, S Tamura, Y Kaneko, T Kuroiwa, Y Tsukada, A Maezawa, Y Nojima.
Abstract
Acquired haemophilia associated with autoimmune disorders can be fatal and has been reported to be refractory to steroid therapy alone. We report two cases of female patients, aged 24 years and 54 years, with acquired haemophilia caused by factor VIII inhibitors. Underlying diseases were systemic lupus erythematosus in the 24-year-old patient and rheumatoid arthritis in the 54-year-old patient. Both conditions were nearly quiescent when the patients manifested haemorrhagic diathesis. In response to combination therapy with prednisolone and cyclophosphamide, coagulation abnormalities were resolved together with complete elimination of factor VIII inhibitors in both patients. Thus, combination therapy with alkylating agents may be recommended as initial therapy for the management of autoimmune patients with factor VIII inhibitors.Entities:
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Year: 2001 PMID: 11725831 DOI: 10.1177/147323000102900508
Source DB: PubMed Journal: J Int Med Res ISSN: 0300-0605 Impact factor: 1.671