Bone and joint manifestations of sickle cell anaemia
- 1 May 1990
- journal article
- research article
- Published by British Editorial Society of Bone & Joint Surgery in The Journal of Bone and Joint Surgery. British volume
- Vol. 72-B (3) , 494-499
- https://doi.org/10.1302/0301-620x.72b3.2341455
Abstract
We investigated 57 patients with sickle cell anaemia (HbSS) and bone and joint changes. Osteonecrosis simulating a wide range of conditions was a common radiological feature, and osteomyelitis occurred in 61% of cases. Salmonella species were the commonest causative organisms, occurring in 71% of patients with osteomyelitis, although salmonella septic arthritis occurred in only two. The distinction between vaso-occlusive bone crisis and acute osteomyelitis was often difficult since the classical clinical and radiological features and laboratory findings also occurred in bone infarction, a common feature of the disease.This publication has 3 references indexed in Scilit:
- Salmonella osteomyelitis in childhood. A report of 63 cases seen in Nigerian children of whom 57 had sickle cell anaemia.Archives of Disease in Childhood, 1980
- Natural History of Sickle Cell Anemia in Saudi ArabsAnnals of Internal Medicine, 1978
- Arthropathy in Sickle-Cell DiseaseAnnals of Internal Medicine, 1973