Gilchrist G S, Hagedorn A B, Stauffer R N
JAMA. 1977 Nov 28;238(22):2383-5.
Severe degenerative joint disease developed in three adults with mild to moderately severe hemophilia A, as judged by the clinical course and by levels of factor VIII coagulant. Bilateral total hip arthroplasty was required in one patient, unilateral hip arthroplasty in the second, and a recommendation for bilateral knee replacement in the third. The pathogenesis of the arthropathy may be multifactorial and the result of repeated joint hemorrhage that remains unrecognized and inadequately treated. These observations suggest the need for more careful monitoring of patients who have relatively mild hemophilia.
三名患有轻度至中度严重甲型血友病的成年人出现了严重的退行性关节疾病,这是根据临床病程和凝血因子 VIII 水平判断得出的。一名患者需要进行双侧全髋关节置换术,第二名患者进行单侧髋关节置换术,第三名患者则被建议进行双侧膝关节置换术。关节病的发病机制可能是多因素的,是反复关节出血未被识别和治疗不充分的结果。这些观察结果表明,需要对患有相对轻度血友病的患者进行更仔细的监测。