Massive septic pelvic osteolysis following revision total hip arthroplasty in a patient with sickle cell anemia: clinical presentation and review of the literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Orthopedics and Sports Medicine,Surgery
Link
http://link.springer.com/content/pdf/10.1007/s00590-011-0875-x.pdf
Reference22 articles.
1. Keeley K, Buchanan GR (1982) Acute infraction of long bones in children with sickle cell anemia. J Pediatr 101:170–175
2. Styles LA, Vichinsky EP (1996) Core decompression in avascular necrosis of the hip in sickle-cell disease. Am J Hematol 52:103–107
3. Vichinsky EP, Neumayr LD, Haberkern C, Earles AN, Eckman J, Koshy M, Black DM (1999) The perioperative complication rate of orthopaedic surgery in sickle cell disease: report of the national sickle cell surgery study group. Am J Hematol 62(3):129–138
4. Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP (1994) Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 330(23):1639–1644
5. Al Mousawi F, Malki A, Al-Aradi A, Al-Bagali M, Al-Sadadi A, Booz MM (2002) Total hip replacement in sickle cell disease. Int Orthop 26(3):157–161
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1. Movement Is Life—Optimizing Patient Access to Total Joint Arthroplasty: Anemia and Sickle Cell Disease Disparities;Journal of the American Academy of Orthopaedic Surgeons;2022-03-18
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