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Ann Hematol Oncol. 2017; 4(3): 1142.
Dactylitis as an Earty Onset of Sickle Cell Disease Pain
Cela E*, Aguilar Y, García-Morín M and Beléndez C
Hematología Pediátrica, Hospital General Universitario Gregorio MaraÑón, Spain
*Corresponding author: Elena Cela, Hematología Pediátrica, Hospital General Universitario Gregorio Marañón, Madrid, Spain
Received: February 07, 2017; Accepted: February 27, 2017; Published: March 13, 2017
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A 12-month-old child with homozygous sickle cell disease diagnosed at birth consulted at the hospital because of limited manual dexterity and crying out in apparent pain for a few days. No other symptom was referred. A previous medical assessment had been unremarkable. On physical examination, the patient was stable, a febrile, with normal vital signs. He had swelling on the dorsal aspect of the right hand with no other signs of inflammation. The remaining exam was uneventful. A radiographic examination revealed a periostic reaction at the 3rd and 5th metacarpal bones. A diagnosis of dactylitis was made and the child was treated with oral analgesics, anti-inflammatories and hydration at home.
Dactylitis are episodes of vaso-occlusive pain in small bones of the hands and feet that develop in children during the first 4 years of life, before the haematopoietic tissue in these locations is replaced by fibrous connective tissue and fat. Osteomyelitis should be considered in the differential diagnosis.