Vij Mukul, Agrawal Vinita, Jain Manoj
Department of Pathology, Global Health City, Chennai, Tamilnadu, India.
Saudi J Kidney Dis Transpl. 2014 Jul;25(4):844-8. doi: 10.4103/1319-2442.135177.
Mixed connective tissue disease (MCTD) is an overlap syndrome first defined in 1972 by Sharp et al. In this original study, the portrait emerged of a connective tissue disorder sharing features of systemic lupus erythematosus, systemic sclerosis (scleroderma) and polymyositis. Scleroderma renal crisis (SRC) is an extremely infrequent but serious complication that can occur in MCTD. The histologic picture of SRC is that of a thrombotic micro-angiopathic process. Renal biopsy plays an important role in confirming the clinical diagnosis, excluding overlapping/superimposed diseases that might lead to acute renal failure in MCTD patients, helping to predict the clinical outcome and optimizing patient management. We herewith report a rare case of SRC in a patient with MCTD and review the relevant literature.
混合性结缔组织病(MCTD)是一种重叠综合征,于1972年由夏普等人首次定义。在这项最初的研究中,出现了一种结缔组织疾病的特征,它兼具系统性红斑狼疮、系统性硬化症(硬皮病)和多发性肌炎的特点。硬皮病肾危象(SRC)是MCTD中一种极为罕见但严重的并发症。SRC的组织学表现为血栓性微血管病变过程。肾活检在确诊临床诊断、排除可能导致MCTD患者急性肾衰竭的重叠/叠加疾病、帮助预测临床结局以及优化患者管理方面发挥着重要作用。我们在此报告一例MCTD患者发生SRC的罕见病例,并回顾相关文献。