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Bilateral Forearm Pseudotumors in an Adult with Hemophilia A and Ollier Disease

A Case Report

Gurbani, Barkha, MD, MPH1; Igbinigie, Matthew, BS1; Koutrouvelis, Aristides, MD1; Alperin, Jack B., MD, FACP1; Lindsey, Ronald W., MD1

doi: 10.2106/JBJS.CC.17.00234
Case Reports
Disclosures

Case: A 29-year-old man with mild hemophilia A and Ollier disease presented with bilateral atraumatic forearm pseudotumors. Both forearm pseudotumors were successfully treated surgically with staged radical extirpation and factor VIII replacement therapy.

Conclusion: Pseudotumors typically occur in adolescents with severe, poorly controlled hemophilia A. The development of factor VIII replacement therapy has progressively reduced the incidence of pseudotumors in patients in the developed world. No standardized therapy exists for pseudotumors that continue to bleed into the muscles despite nonoperative measures. Persistent masses require surgical removal with careful preoperative planning and a team approach.

1Department of Orthopaedic Surgery and Rehabilitation, University of Texas Medical Branch at Galveston, Galveston, Texas

Copyright © 2018 by The Journal of Bone and Joint Surgery, Incorporated
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