Suppr超能文献

诊断系统性红斑狼疮患者产后肾功能不全中非典型溶血性尿毒症综合征的至关重要性:一例报告及全面综述

The Critical Importance of Diagnosing Atypical Hemolytic Uremic Syndrome in Postpartum Renal Dysfunction in a Patient With Systemic Lupus Erythematosus: A Case Report and Comprehensive Review.

作者信息

Inatomi Ayako, Tokoro Shinsuke, Katsura Daisuke, Sawai Toshihiro, Murakami Takashi

机构信息

Department of Obstetrics and Gynecology, Shiga University of Medical Science, Otsu, JPN.

Department of Pediatrics, Shiga University of Medical Science, Otsu, JPN.

出版信息

Cureus. 2025 Feb 14;17(2):e78989. doi: 10.7759/cureus.78989. eCollection 2025 Feb.

Abstract

This case report describes a rare instance of a 33-year-old woman with systemic lupus erythematosus (SLE) who experienced a pregnancy complicated by preeclampsia, eclampsia, and postpartum atypical hemolytic uremic syndrome (aHUS). At 28 weeks and four days of gestation, the patient presented with severe hypertension, proteinuria, and a loss of consciousness, leading to an emergency cesarean section. Postoperatively, the patient developed acute kidney injury, respiratory failure, and thrombotic microangiopathy (TMA). Although she exhibited the classic triad of hemolytic anemia, thrombocytopenia, and renal dysfunction, normal complement levels ruled out postpartum exacerbation of SLE, and aHUS was not diagnosed during hospitalization. Differential diagnoses, including HELLP (Hemolysis, Elevated Liver Enzyme levels, and Low Platelet levels) syndrome, thrombotic thrombocytopenic purpura, and Shiga toxin-producing Escherichia coli (STEC)-HUS, were excluded. Schistocytes appeared on postoperative day 5, leading to the cessation of tacrolimus and the initiation of prednisolone. Continuous hemodiafiltration and mechanical ventilation facilitated gradual recovery, and the patient was discharged on postoperative day 26. Post-discharge genetic testing revealed no pathogenic mutations; however, the clinical presentation supported a diagnosis of aHUS. aHUS driven by excessive complement activation requires prompt recognition and treatment with plasma exchange or anti-complement monoclonal antibodies (e.g., eculizumab). In this case, delayed recognition of aHUS precluded the use of such therapies. This case highlights the importance for clinicians to consider the possibility of aHUS in postpartum patients with severe renal dysfunction and TMA symptoms, even if the patient has an underlying SLE, as early diagnosis and treatment of aHUS is necessary to improve maternal outcomes.

摘要

本病例报告描述了一名33岁系统性红斑狼疮(SLE)女性的罕见病例,该患者妊娠合并子痫前期、子痫和产后非典型溶血尿毒综合征(aHUS)。妊娠28周零4天时,患者出现严重高血压、蛋白尿和意识丧失,遂紧急行剖宫产术。术后,患者出现急性肾损伤、呼吸衰竭和血栓性微血管病(TMA)。尽管她表现出溶血性贫血、血小板减少和肾功能不全的典型三联征,但补体水平正常排除了SLE产后加重,住院期间未诊断出aHUS。排除了包括HELLP(溶血、肝酶升高和血小板减少)综合征、血栓性血小板减少性紫癜和产志贺毒素大肠杆菌(STEC)-HUS在内的鉴别诊断。术后第5天出现裂体细胞,导致他克莫司停用并开始使用泼尼松龙。持续血液透析滤过和机械通气促进了患者的逐渐康复,患者于术后第26天出院。出院后基因检测未发现致病突变;然而,临床表现支持aHUS的诊断。由补体过度激活驱动的aHUS需要及时识别并用血浆置换或抗补体单克隆抗体(如依库珠单抗)治疗。在本病例中,aHUS的延迟识别排除了此类治疗的使用。该病例强调了临床医生对于产后出现严重肾功能不全和TMA症状的患者,即使其患有潜在的SLE,也需考虑aHUS可能性的重要性,因为aHUS的早期诊断和治疗对于改善孕产妇结局是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9220/11910887/cf91f1b1b9bb/cureus-0017-00000078989-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验