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A case-based narrative review of pregnancy-associated atypical hemolytic uremic syndrome/complement-mediated thrombotic microangiopathy.
Che, Michael; Moran, Sarah M; Smith, Richard J; Ren, Kevin Y M; Smith, Graeme N; Shamseddin, M Khaled; Avila-Casado, Carmen; Garland, Jocelyn S.
  • Che M; Division of Nephrology, Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Moran SM; Department of Nephrology, Cork University, Cork, Ireland.
  • Smith RJ; University of Iowa Molecular Otolaryngology and Renal Research Laboratories, Iowa City, Iowa, USA.
  • Ren KYM; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
  • Smith GN; Department of Obstetrics and Gynecology, Queen's University, Kingston, Ontario, Canada.
  • Shamseddin MK; Division of Nephrology, Department of Medicine, Queen's University, Kingston, Ontario, Canada.
  • Avila-Casado C; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; University Health Network, Toronto General Hospital, Toronto, Ontario, Canada.
  • Garland JS; Division of Nephrology, Department of Medicine, Queen's University, Kingston, Ontario, Canada. Electronic address: garlandj@queensu.ca.
Kidney Int ; 105(5): 960-970, 2024 May.
Article en En | MEDLINE | ID: mdl-38408703
ABSTRACT
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microangiopatías Trombóticas / Síndrome Hemolítico Urémico Atípico Límite: Adult / Female / Humans / Pregnancy Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microangiopatías Trombóticas / Síndrome Hemolítico Urémico Atípico Límite: Adult / Female / Humans / Pregnancy Idioma: En Año: 2024 Tipo del documento: Article