Journal of Yeungnam Medical Science
- 제28권2호
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- Pages.202-205
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- 2011
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- 2799-8010(eISSN)
Hypomyopathic Dermatomyositis 1예
A Case of Hypomyopathic Dermatomyositis
- 김현태 (포항성모병원 내과) ;
- 이현욱 (포항성모병원 내과) ;
- 권병진 (포항성모병원 내과) ;
- 이지은 (포항성모병원 내과) ;
- 오동호 (포항성모병원 내과) ;
- 손민수 (포항성모병원 내과) ;
- 최정란 (포항성모병원 류마티스.재활센터)
- Kim, Hyun-Tae (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Lee, Hyun-Wook (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Kwon, Byung-Jin (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Lee, Ji-Eun (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Oh, Dong-Ho (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Sohn, Min-Su (Department of Internal Medicine, Pohang Saint Mary's Hospital) ;
- Choi, Jung-Ran (Rheumatology.Rehabilitation Center, Pohang Saint Mary's Hospital)
- 발행 : 2011.12.30
초록
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.