A case-based narrative review of pregnancy-associated atypical hemolytic uremic syndrome/complement-mediated thrombotic microangiopathy

被引:6
作者
Che, Michael [1 ]
Moran, Sarah M. [2 ]
Smith, Richard J. [3 ]
Ren, Kevin Y. M. [4 ]
Smith, Graeme N. [5 ]
Shamseddin, M. Khaled [6 ]
Avila-Casado, Carmen [7 ,8 ]
Garland, Jocelyn S.
机构
[1] Univ Ottawa, Dept Med, Div Nephrol, Ottawa, ON, Canada
[2] Cork Univ Hosp, Dept Nephrol, Cork, Ireland
[3] Univ Iowa, Mol Otolaryngol & Renal Res Labs, Iowa City, IA USA
[4] Queens Univ, Dept Pathol & Mol Med, Kingston, ON, Canada
[5] Queens Univ, Dept Obstet & Gynecol, Kingston, ON, Canada
[6] Queens Univ, Dept Med, Div Nephrol, Kingston, ON, Canada
[7] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[8] Univ Hlth Network, Toronto Gen Hosp, Toronto, ON, Canada
关键词
atypical hemolytic uremic syndrome; C5; inhibitor; complement testing; complement-mediated thrombotic microangiopathy; placental biomarkers; pregnancy; PLACENTAL GROWTH-FACTOR; ELEVATED LIVER-ENZYMES; COMPLEMENT ACTIVATION; SUPERIMPOSED PREECLAMPSIA; ECULIZUMAB; WOMEN; DIAGNOSIS; C5B-9; AHUS; DYSREGULATION;
D O I
10.1016/j.kint.2023.12.021
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Atypical hemolytic uremic syndrome is a complement- mediated thrombotic microangiopathy caused by uncontrolled activation of the alternative complement pathway in the setting of autoantibodies to or rare pathogenic genetic variants in complement proteins. Pregnancy may serve as a trigger and unmask atypical hemolytic uremic syndrome/complement-mediated thrombotic microangiopathy (aHUS/CM-TMA), which has severe, life-threatening consequences. It can be difficult to diagnose aHUS/CM-TMA in pregnancy due to overlapping clinical features with other thrombotic microangiopathy syndromes including hypertensive disorders of pregnancy. However, the distinction among thrombotic microangiopathy etiologies in pregnancy is important because each syndrome has specific disease management and treatment. In this narrative review, we discuss 2 cases to illustrate the diagnostic challenges and evolving approach in the management of pregnancy-associated aHUS/CM-TMA. The first case involves a 30-year-old woman presenting in the first trimester who was diagnosed with aHUS/CM-TMA and treated with eculizumab from 19 weeks' gestation. Genetic testing revealed a likely pathogenic variant in CFI. She successfully delivered a healthy infant at 30 weeks' gestation. In the second case, a 22-year-old woman developed severe postpartum HELLP syndrome, requiring hemodialysis. Her condition improved with supportive management, yet investigations assessing for aHUS/CM-TMA remained abnormal 6 months postpartum consistent with persistent complement activation but negative genetic testing. Through detailed case discussion describing tests assessing for placental health, fetal anatomy, complement activation, autoantibodies to complement regulatory proteins, and genetic testing for aHUS/CM-TMA, we describe how these results aided in the clinical diagnosis of pregnancy-associated aHUS/CM-TMA and assisted in guiding patient management, including the use of anticomplement therapy.
引用
收藏
页码:960 / 970
页数:11
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