Melissaropoulos Konstantinos, Georgiou Panagiotis
Department of Rheumatology, Agios Andreas General Hospital, Patras, Greece.
Mediterr J Rheumatol. 2021 Dec 27;32(4):358-362. doi: 10.31138/mjr.32.4.358. eCollection 2021 Dec.
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease, and haematologic manifestations are part of its spectrum. Herein, we report a case of a patient with a long-standing diagnosis of SLE, presenting with thrombotic thrombocytopenic purpura (TTP) and acute renal failure, without co-existent clinical and laboratory markers of disease activity, causing diagnostic questions. A short literature review concerning TTP and SLE is also presented. TTP is a rare syndrome of thrombotic microangiopathy, which represents a medical urgency and carries significant morbidity and mortality if left untreated. SLE has been correlated with the occurrence of TTP, often with atypical presentation and worse prognosis.
系统性红斑狼疮(SLE)是一种多系统自身免疫性疾病,血液学表现是其临床表现的一部分。在此,我们报告一例长期诊断为SLE的患者,该患者出现血栓性血小板减少性紫癜(TTP)和急性肾衰竭,且不存在疾病活动的临床和实验室指标,这引发了诊断方面的问题。本文还对有关TTP和SLE的文献进行了简要综述。TTP是一种罕见的血栓性微血管病综合征,是一种医疗急症,如果不治疗,会有很高的发病率和死亡率。SLE与TTP的发生相关,通常表现不典型且预后较差。