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Acquired Haemophilia A in Association with Influenza A and Urinary Tract Infection. | LitMetric

AI Article Synopsis

  • Acquired haemophilia A (AHA) is a rare autoimmune disorder primarily affecting factor VIII, leading to complications like life-threatening bleeding, which often goes undiagnosed due to low awareness.
  • An 85-year-old woman developed symptoms of respiratory infection that progressed to haematuria and required transfusions; lab results indicated prolonged aPTT and high inhibitor titres, necessitating comprehensive treatment.
  • Early diagnosis and effective management, including immunosuppressive drugs, are critical for remission and preventing recurrence, especially when other infections, like influenza A, are involved.

Article Abstract

Unlabelled: Acquired haemophilia A (AHA) is a rare autoimmune disorder caused by an autoantibody against any circulating coagulation factor, especially factor VIII (FVIII). The lack of awareness of this condition suggests that diagnosis is a challenge and usually delayed, which leads to suboptimal treatment. Consequently, early diagnosis is mandatory to prevent potentially life-threatening bleeding complications. We present the case of an 85-year-old woman admitted to hospital with symptoms of respiratory infection who 12 hours later developed haematuria which required transfusion. Laboratory assays showed an isolated prolonged aPTT, a moderately reduced FVIII and a high inhibitor titre. Influenza A and were also identified. Antivirals, antibiotics, immunosuppressive drugs and haemostatic agents were started. Two weeks later, the inhibitor was not detected, and bleeding and symptoms of infection had resolved. Immunosuppressive drugs were stopped on day 45 and there has been no recurrence since then. To date, no FVIII inhibitors have been reported in concomitant infection with influenza A and urinary The identification of conditions potentially associated with AHA is essential to achieve complete remission.

Learning Points: The lack of awareness of and experience with acquired haemophilia (AHA) suggests that diagnosis is frequently delayed, resulting in suboptimal treatment.AHA should be suspected in recent-onset abnormal bleeding in patients not receiving anticoagulant treatment, and in the presence of isolated prolonged activated partial thromboplastin time (aPTT).Treatment is based on eradication of the inhibitor, control of the bleeding and identification of underlying conditions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473680PMC
http://dx.doi.org/10.12890/2020_001678DOI Listing

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