Dactylitis: A Complication in Patients With Sickle Cell Disease
Department of Haematology Laboratory Specialties, Amiri Hospital, Kuwait
Citation: Salma AlDallal. “Dactylitis: A Complication in Patients With Sickle Cell Disease”. American Research
Journal of Hematology; 1(1): 27-31.
Abstract
Abstract: Sickle cell disease (SCD) is a group of disorders that affects hemoglobin, the red pigment in blood
erythrocytes responsible for delivering oxygen throughout the body. This is the most commonly inherited blood
disorder. One of the most widespread manifestations of SCD is painful vaso-occlusive crises and osteomyelitis.
Dactylitis or hand-foot syndrome is the first clinical sign of SCD among children under the age of 6 years,
particularly for those aged 1-2 years. Sickle cell dactylitis, an acute vaso-occlusive condition is associated with
pain and edema on the dorsum of hands or feet or both simultaneously, along with elevated local temperature
and erythema. This review will detail the problems associated with the bone and skeletal involvement in SCD
with specific emphasis on dactylitis in children; description of its signs, symptoms, effects, as well as treatment
procedure.