Vaishya Raju, Agarwal Amit Kumar, Edomwonyi Edwin O, Vijay Vipul
Orthopaedics, Indraprastha Apollo Hospital.
Orthopaedics, Irrua Specialist Teaching Hospital.
Cureus. 2015 Oct 20;7(10):e358. doi: 10.7759/cureus.358.
Sickle cell disease (SCD) is an inherited disorder of abnormal haemoglobin commonly encountered in the West African sub-region. It has varied osteoarticular and non-osseous complications that mimic some surgical conditions. The most common orthopaedic complications include avascular necrosis, osteomyelitis, septic arthritis, etc. A cautious and painstaking evaluation is required in handling these patients. Acute care and anaesthetic precautions are vital in ensuring an uneventful postoperative period.
镰状细胞病(SCD)是一种常见于西非次区域的遗传性异常血红蛋白疾病。它有多种骨关节和非骨并发症,可模仿一些外科疾病。最常见的骨科并发症包括缺血性坏死、骨髓炎、化脓性关节炎等。在处理这些患者时需要谨慎和细致的评估。急性护理和麻醉预防措施对于确保术后顺利恢复至关重要。