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Case Reports
. 2005 Dec 30;11(4):11.

Juvenile amyopathic dermatomyositis

J Scott Henning  1 , Agnieszka Witkiewicz, Julie V Schaffer, Seth J Orlow
Affiliations
  • PMID: 16403383
Case Reports

Juvenile amyopathic dermatomyositis

J Scott Henning et al. Dermatol Online J. .

Abstract

A 3-year-old girl presented with a 6-month history of multiple, light-pink, flat-topped papules over the dorsal aspects of the metacarpophalangeal and interphalangeal joints of the hands and feet. Nailfold telangiectases, ragged cuticles, and a heliotrope color of the upper eyelids were also evident, but there was no clinical evidence of muscle weakness and levels of muscle enzymes were normal. A biopsy specimen from one of the papules showed a vacuolar interface dermatitis consistent with a diagnosis of dermatomyositis. This report draws attention to juvenile amyopathic dermatomyositis, which is an uncommon subtype of dermatomyositis with an excellent prognosis.

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