Lally E V, Buckley W M, Claster S
J Rheumatol. 1983 Oct;10(5):813-6.
Bone and joint abnormalities occur frequently in sickle cell anemia but are rare in sickle cell trait. Long bone diaphyseal infarctions are distinctly unusual in sickle cell trait. We describe a patient with AS hemoglobin and symptomatic bone infarctions in the diaphyses and metadiaphyses of the long bones of the lower extremities and in the calcaneus. In addition, this patient manifested noninflammatory synovial effusions of the knee. The bone and joint manifestations of sickle cell trait are reviewed in the context of this case.
骨骼和关节异常在镰状细胞贫血中很常见,但在镰状细胞性状中很少见。长骨干骺端梗死在镰状细胞性状中明显不常见。我们描述了一名患有AS血红蛋白的患者,其下肢长骨骨干和干骺端以及跟骨出现有症状的骨梗死。此外,该患者还表现出膝关节的非炎性滑膜积液。结合该病例对镰状细胞性状的骨骼和关节表现进行了综述。