Anti-MDA5 Antibody-Positive Dermatomyositis

Authors

  • Naruedee Potear DIVISION OF DERMATOLOGY, DEPARTMENT OF MEDICINE, PHRAMONGKUTKLAO HOSPITAL, BANGKOK, THAILAND.
  • Supitchaya Thaiwat DIVISION OF DERMATOLOGY, DEPARTMENT OF MEDICINE, PHRAMONGKUTKLAO HOSPITAL, BANGKOK, THAILAND.

Keywords:

Anti-MDA5 dermatomyositis

Abstract

Dermatomyositis is an autoimmune disease, in which positive anti-melanoma differentiation associated gene 5 (anti-MDA5) is known as serious subtype, that might develop mucocutaneous lesions, vascular occlusion, and rapidly progressive interstitial lung disease. We report case series of three middle-aged female dermatomyositis patients with positive anti-MDA5 serology. All of the patients had mucocutaneous lesions, composed of cutaneous ulcers together with Gottron’s papules, and rapidly progressive interstitial lung disease. Histopathology of the ulcerated skin showed vascular thrombosis that was a common finding in this subtype. Patients were treated with several immunosuppressive drugs such as high-dose glucocorticoid, intravenous cyclophosphamide and azathioprine, however the disease progressed and two patients succumbed to their illnesses.

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Published

2019-10-01

How to Cite

Potear, N., & Thaiwat, S. (2019). Anti-MDA5 Antibody-Positive Dermatomyositis. Thai Journal of Dermatology, 35(3), 119–127. Retrieved from https://he02.tci-thaijo.org/index.php/TJD/article/view/163095