血管紧张素转换酶抑制剂成功治疗混合性结缔组织病硬皮病肾危重1例。

Case Reports in Nephrology Pub Date : 2021-01-06 eCollection Date: 2021-01-01 DOI:10.1155/2021/8862405
Jomana Madieh, Iman Khamayseh, Alaa Hrizat, Abdurrahman Hamadah, Kamel Gharaibeh
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引用次数: 2

摘要

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病综合征。MCTD的一个极其罕见但严重的并发症是硬皮病肾危象(SRC)。治疗与MCTD相关的SRC有不同的方法。我们报告一例MCTD伴雷诺氏现象、皮肌炎和血小板减少合并急性SRC的慢性特征,对ACE抑制剂表现出很大的反应。在这里,我们建议一旦怀疑有SRC,尽早积极使用ACE抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Scleroderma Renal Crisis in a Case of Mixed Connective Tissue Disease Treated Successfully with Angiotensin-Converting Enzyme Inhibitors.

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.

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来源期刊
Case Reports in Nephrology
Case Reports in Nephrology Medicine-Nephrology
CiteScore
1.70
自引率
0.00%
发文量
32
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