Bilateral total knee replacement for hemophilic arthropathy: a case report
- PMID: 40281505
- PMCID: PMC12023443
- DOI: 10.1186/s12891-025-08611-1
Bilateral total knee replacement for hemophilic arthropathy: a case report
Abstract
Von Willebrand disease (vWD) and hemophilia present unique challenges in orthopedic surgery due to their inherent bleeding risks and potential complications. While joint bleedings are well-documented in hemophilia, they are less understood in vWD, especially regarding their impact on daily activities and the development of arthropathy. We present a case of a young female patient aged 25 years with vWD Type 3 who underwent bilateral total knee replacement (TKR) due to end-stage knee osteoarthritis. Following two previous operations of the right knee at the age of 14, the patient had high degree of extra-articular valgus and intra-articular deformity, ankylosed knee in 30o flexion, osteopenia, and chronic patellar dislocation. Bilateral TKR was performed using patient-specific templating (PST) technology, which includes preoperative planning using a CT scan followed by surgical execution. Financial constraints and limited prosthetic resources necessitated a sequential approach to TKR, addressing the more affected right knee first. Despite many challenges, successful outcomes were achieved, with significant improvements in pain, mobility, overall satisfaction, and no complications at two-year follow-up. Our case highlights the importance of individualized treatment strategies, meticulous surgical planning, and postoperative care in managing knee arthropathy patients with bleeding disorders.
Keywords: Fused knee arthroplasty; Patient-specific templating; Total knee replacement; Valgus deformity; Von Willebrand disease.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: Ethical approval was obtained from the Ethical Committee of October 6 University Hospital. Consent for publication: The involved patient signed a written consent form for the publication of her personal and clinical data as well as her radiographic images. Competing interests: All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge, or beliefs) in the subject matter or materials discussed in this manuscript. Consent to participate: The involved patient signed a written informed consent.
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References
-
- Leebeek FW, Eikenboom JC. Von Willebrand’s disease. N Engl J Med. 2016;375(21):2067–80. 10.1056/NEJMra1601561. - PubMed
-
- de Wee EM, Sanders YV, Mauser-Bunschoten EP, van der Bom JG, Degenaar-Dujardin ME, Eikenboom J, et al. Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease. Thromb Haemost. 2012;108(4):683–92. 10.1160/TH12-04-0244. - PubMed
-
- Mahlangu J, Diop S, Lavin M. Diagnosis and treatment challenges in lower resource countries: State-of-the-art. Haemophilia. 2024;30(Suppl 3):78–85. 10.1111/hae.14956. - PubMed
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