Amyopathic dermatomyositis.

N. J. Olsen, J. H. Park, L. E. King

Research output: Contribution to journalReview articlepeer-review

17 Scopus citations

Abstract

Amyopathic dermatomyositis is a variant of dermatomyositis that is characterized by the typical skin rash but without the muscle abnormalities. It has been proposed that the amyopathic and myopathic forms of dermatomyositis exist on a continuum, a concept that is supported by family and genetic studies and the observation that a small proportion of amyopathic patients transform to a frankly myopathic state. The amyopathic state is defined by a lack of muscle weakness and through diagnostic tests, including serum muscle enzymes, electromyogram studies, and muscle biopsies, that are usually normal or show only minimal abnormalities. Despite the lack of weakness, many patients complain of debilitating fatigue. More sensitive measures of muscle function, such as P-31 magnetic resonance spectroscopy, suggest that muscle metabolism is abnormal in amyopathic patients. The amyopathic form is more commonly seen in adults than in children, although juvenile cases are reported. Some early series suggested no association with underlying malignancies, but recent reports indicate that malignancies occur. Determining whether a patient has amyopathic rather than myopathic disease may have prognostic implications.

Original languageEnglish (US)
Pages (from-to)346-351
Number of pages6
JournalCurrent rheumatology reports
Volume3
Issue number4
DOIs
StatePublished - Aug 2001

All Science Journal Classification (ASJC) codes

  • Rheumatology

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