Ichiki Y, Akiyama T, Shimozawa N, Suzuki Y, Kondo N, Kitajima Y
Department of Dermatology and Department of Paediatrics, School of Medicine, Gifu University, 40 Tsukasa-machi, Gifu 500-8705, Japan.
Br J Dermatol. 2001 Apr;144(4):894-7. doi: 10.1046/j.1365-2133.2001.04153.x.
A case of cutaneous calcinosis associated with juvenile dermatomyositis is described. The patient was a 3-year-old girl who had been diagnosed as having dermatomyositis at age 1 year. She was treated with prednisolone, but developed multiple calcified nodules in the subcutaneous tissues and intermuscular fascia. These nodules gradually increased in size despite continual therapy with steroids and aluminium hydroxide. Treatment with diltiazem completely suppressed the development of calcinosis.
报告了一例与幼年皮肌炎相关的皮肤钙质沉着症病例。患者为一名3岁女童,1岁时被诊断为皮肌炎。她接受了泼尼松龙治疗,但皮下组织和肌间筋膜出现了多个钙化结节。尽管持续使用类固醇和氢氧化铝治疗,这些结节仍逐渐增大。地尔硫卓治疗完全抑制了钙质沉着症的发展。