Acquired factor VIII inhibitor in a patient with dermatomyositis - A case study

Ayodele Ayoola, Wajahath Mohsini, Sein Aung

    Research output: Contribution to journalArticlepeer-review

    4 Scopus citations


    Background: Acquired factor VIII inhibitor is an antibody formed against FVIII and seen in patients without FVIII replacement therapy. This entity has been associated with both autoimmune disease and infections. Case Study: We report the case of a 65-year-old man with dermatomyositis who presented with a bleeding episode following venipuncture and hematuria. His coagulation parameters were followed as well as the inhibitor level. His acquired FVIII inhibitor was managed successfully with rituximab. Conclusion: Our patient's bleeding episodes resolved and the inhibitor level was undetectable after 12 months. This is the first case of acquired FVIII inhibitor in association with dermatomyositis.

    Original languageEnglish (US)
    Pages (from-to)8-11
    Number of pages4
    JournalActa Haematologica
    Issue number1
    StatePublished - Mar 1 2008

    All Science Journal Classification (ASJC) codes

    • Hematology


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