Yuste Claudia, Rapalai Molefe, Pritchard Benjamin A, Jones Terence J, Amoasii Constanza, Al-Ansari Atheer, Ramakrishna Satish B
Shrewsbury and Telford NHS Trust , Shorpshire , UK.
Clin Kidney J. 2014 Feb;7(1):59-61. doi: 10.1093/ckj/sft142. Epub 2013 Dec 23.
We present the second report of the association between antineutrophil cytoplasm antibodies (ANCA)-associated vasculitis with dermatomyositis (DM). A 47-year-old woman suddenly developed rapidly progressive renal failure in the context of (DM). The kidney biopsy showed focal and segmental necrotizing glomerulonephritis with crescent formation. Cyclophosphamide treatment was commenced resulting in a significant recovery of kidney function and maintenance of recovery at 6 months. Although the pathophysiology is unknown, we hypothesize that CD8-T-deficient cells and MPO+ neutrophils in the DM lesions play an important role in the disease process.
我们报告第二例抗中性粒细胞胞浆抗体(ANCA)相关性血管炎合并皮肌炎(DM)的病例。一名47岁女性在患皮肌炎期间突然出现快速进展性肾衰竭。肾脏活检显示局灶节段性坏死性肾小球肾炎伴新月体形成。开始使用环磷酰胺治疗后,肾功能显著恢复,并在6个月时维持恢复状态。尽管其病理生理机制尚不清楚,但我们推测皮肌炎病变中的CD8-T缺陷细胞和MPO+中性粒细胞在疾病过程中起重要作用。