Abstract
A 55-year-old male presented to our emergency department with haematuria and abdominal pain. Investigations including a computed tomography (CT) scan revealed an intraluminal filling defect within the left collecting system, consistent in appearance with blood clot. With an initial working diagnosis of upper tract urothelial cell carcinoma, he was discharged with plans for an urgent cystoscopy and ureteroscopy. He subsequently represented with ongoing frank haematuria, anasarca, dropping haemoglobin and new right collecting system blood clot. Subsequent investigations showed that the patient had acquired haemophilia A resulting in the episodes of haematuria, highlighted after an elevated activated partial thromboplastic time prompted a thrombophilia screen. The patient was subsequently treated with factor eight inhibitor bypass activity, corticosteroids and cyclophosphamide.
Reference5 articles.
1. Acquired hemophilia A: a rare cause of gross hematuria;Hosier;Can Urol Assoc J,2015
2. Coutre S . Acquired inhibitors of coagulation; Steven Coutre, 2019. Available: https://www.uptodate.com/contents/acquired-inhibitors-of-coagulation [Accessed May 2020].
3. Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)
4. Acquired hemophilia A: emerging treatment options;Janbain;J Blood Med,2015
5. Acquired hemophilia A: updated review of evidence and treatment guidance;Kruse-Jarres;Am J Hematol,2017
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