Yeungnam Univ J Med.  2011 Dec;28(2):202-205.

A Case of Hypomyopathic Dermatomyositis

Affiliations
  • 1Department of Internal Medicine, Pohang Saint Mary's Hospital, Pohang, Korea.
  • 2Rheumatology, Rehabilitation Center, Pohang Saint Mary's Hospital, Pohang, Korea. ranchannel@hotmail.com

Abstract

Dermatomyositis is a rare and idiopathic inflammatory myopathy with a characteristic cutaneous manifestation. A 62-year-old female complained of polyarthralgia that lasted for many years. She was diagnosed with hypomyopathic dermatomyositis by the typical skin rash associated with dermatomyositis but without muscle involvement such as muscle weakness, elevated level of creatinine phosphokinase and aldolase. Her symptoms improved with treatment of hydroxychloroquine and prednisolone. We experienced a case of hypomyopathic dermatomyositis on 62-year-old female patient and report with review of literatures.

Keyword

Dermatomyositis

MeSH Terms

Arthralgia
Creatinine
Dermatomyositis
Exanthema
Female
Fructose-Bisphosphate Aldolase
Humans
Hydroxychloroquine
Middle Aged
Muscle Weakness
Muscles
Myositis
Prednisolone
Creatinine
Fructose-Bisphosphate Aldolase
Hydroxychloroquine
Prednisolone
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