Complex regional pain syndrome type I in children
Article first published online: 10 APR 2008
DOI: 10.1111/j.1651-2227.2008.00744.x
©2008 The Author(s)/Journal Compilation ©2008 Foundation Acta Pædiatrica/Acta Pædiatrica
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How to Cite
Tan, E. C., Zijlstra, B., Essink, M. L., Goris, R. J. A. and Severijnen, R. S. (2008), Complex regional pain syndrome type I in children. Acta Paediatrica, 97: 875–879. doi: 10.1111/j.1651-2227.2008.00744.x
Publication History
- Issue published online: 2 JUN 2008
- Article first published online: 10 APR 2008
- Received 31 August 2007; revised 31 January 2008; accepted 7 February 2008.
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Keywords:
- Children;
- CRPS I
Abstract
Background: Complex Regional Pain Syndrome type I (CRPS I) is a potentially incapacitating syndrome which can occur after a minor injury or operation to a limb. It is a disorder characterized by pain, sensory and motor disturbances. CRPS I is well known in adults, but a relatively new diagnostic entity in children. The clinical presentation of CRPS I in children is, to some extent, different from adults and therefore sometimes not recognized early. The aim of this study was to search for differences in patient characteristics between children and adults with CRPS I.
Methods: We have performed a retrospective chart review of 78 children (age ≤16 year) with CRPS I and compared the data with those of 951 adults with CRPS I.
Results: The child population consisted predominantly of girls and older children (median age 13 years). The child population differed from adults in that the skin temperature of the involved extremity at onset was more often cooler, the lower extremity was involved more frequently and neurological and sympathetic symptoms were less pronounced.
Conclusions: In several aspects, CRPS I in children has a different presentation than in adults.

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