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The Journal of Bone and Joint Surgery, Vol 58, Issue 8 1161-1163, Copyright © 1976 by Journal of Bone and Joint Surgery, Inc

JOURNAL CONTENTS

Sickle-cell dactylitis

VT Worrall and V Butera

In order to define better the presentation, roentgenographic features, and clinical course of sickle-cell dactylitis, the records of nine children with sickle-cell anemia and acutely painful, swollen digits were reviewed. The average age of these children at the time of diagnosis was eighteen months, and in five instances the dactylitis occurred before the diagnosis of sickle-cell disease was established. The clinical signs, consisting of swelling, tenderness, fever, and leukocytosis, were self-limiting and resolved in five to thirty-one days. The roentgenographic features, characterized by periosteal new-bone formation or intramedullary densities, appeared in seven to fourteen days and resolved in two to three months. Incorrect diagnosis is frequent in this condition but can be avoided as familiarity with the syndrome increases.
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M.C.G. Stevens, M. Padwick, and G.R. Serjeant
Observations on the Natural History of Dactylitis in Homozygous Sickle Cell Disease
Clinical Pediatrics, May 1, 1981; 20(5): 311 - 317.
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