Madieh Jomana, Khamayseh Iman, Hrizat Alaa, Hamadah Abdurrahman, Gharaibeh Kamel
Department of Internal Medicine, Faculty of Medicine, Al-Quds University, Abu Dis, State of Palestine.
Department of Internal Medicine, Faculty of Medicine, Hashemite University, Zarqa, Jordan.
Case Rep Nephrol. 2021 Jan 6;2021:8862405. doi: 10.1155/2021/8862405. eCollection 2021.
Mixed connective tissue disease (MCTD) is a rheumatic disease syndrome with overlapping features of scleroderma, systemic lupus erythematosus, and polymyositis. An extremely rare but serious complication that can occur in MCTD is scleroderma renal crisis (SRC). There have been different approaches to the treatment of SRC associated with MCTD. We present a case of MCTD with chronic features of Raynaud's phenomenon, dermatomyositis, and thrombocytopenia complicated with acute SRC which showed a great response to ACE inhibitors. Here, we advise the early and aggressive use of ACE inhibitors as soon as SRC is suspected.
混合性结缔组织病(MCTD)是一种具有硬皮病、系统性红斑狼疮和多发性肌炎重叠特征的风湿性疾病综合征。MCTD可能出现的一种极其罕见但严重的并发症是硬皮病肾危象(SRC)。对于与MCTD相关的SRC,已有不同的治疗方法。我们报告一例具有雷诺现象、皮肌炎和血小板减少症慢性特征的MCTD患者,其并发急性SRC,对血管紧张素转换酶抑制剂(ACE抑制剂)反应良好。在此,我们建议一旦怀疑SRC,应尽早积极使用ACE抑制剂。