Neuropediatrics 2007; 38(3): 157-159
DOI: 10.1055/s-2007-990265
Short Communication

© Georg Thieme Verlag KG Stuttgart · New York

A Case of Primary Erythermalgia, Wintry Hypothermia and Encephalopathy

K. Takahashi 1 , M. Saitoh 1 , H. Hoshino 1 , M. Mimaki 1 , Y. Yokoyama 1 , M. Takamizawa 1 , M. Mizuguchi 1 , Z.-M. Lin 2 , Y. Yang 2 , T. Igarashi 1
  • 1Department of Pediatrics, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
  • 2Department of Dermatology, Peking University, First Hospital, Beijing, P. R. China
Further Information

Publication History

received 11. 04. 2007

Accepted 09. 08. 2007

Publication Date:
05 November 2007 (online)

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Abstract

Primary erythermalgia is a rare neuropathy characterized by attacks of burning pain and redness in the extremities in response to warm stimuli. We describe here a boy with erythermalgia whose painful attacks began in infancy. We found a novel mutation of SCN9A, which is a responsible gene for primary erythermalgia in this case. In his teens, he developed wintry hypothermia with resultant neurological dysfunction and recurrent pneumonia. During the course of pneumonia, he had transient encephalopaty with a reversible lesion in the splenium of the corpus callosum. In addition to excessive cooling, a defect in central thermoregulation may have caused hypothermia in this patient.