Pregnancy-Associated Atypical Hemolytic Uremic Syndrome: A Case Report with MCP Gene Mutation and Successful Eculizumab Treatment

Bibliographic Details
Title: Pregnancy-Associated Atypical Hemolytic Uremic Syndrome: A Case Report with MCP Gene Mutation and Successful Eculizumab Treatment
Authors: Alex Domínguez-Vargas, Fanny Ariño, Diana Silva, Henry J. González-Tórres, Gustavo Aroca-Martinez, Eduardo Egea, Carlos G. Musso
Source: American Journal of Perinatology Reports, Vol 14, Iss 01, Pp e96-e100 (2024)
Publisher Information: Thieme Medical Publishers, Inc., 2024.
Publication Year: 2024
Collection: LCC:Gynecology and obstetrics
Subject Terms: aHUS, pregnancy, thrombotic microangiopathy, eculizumab, HELLP syndrome, Gynecology and obstetrics, RG1-991
More Details: Pregnancy-associated atypical hemolytic uremic syndrome (P-aHUS) is a rare condition characterized by microangiopathic hemolytic anemia and kidney injury from thrombotic microangiopathy. P-aHUS occurs in approximately 1 in 25,000 pregnancies and is strongly related to complement dysregulation and pregnancy-related disorders, such as preeclampsia, eclampsia, and hemolysis, elevated liver enzymes, low platelet (HELLP) syndrome, resulting in adverse perinatal and fetal outcomes. Complement dysregulation in P-aHUS is commonly attributed to genetic mutations or autoantibodies affecting complement factors, including CFH, CFI, and MCP. We present a case of a 25-year-old primigravida who experienced severe preeclampsia and HELLP syndrome followed by the development of complicated P-aHUS during the early postpartum period. The patient exhibited severe clinical manifestations, including hypertensive emergency, central nervous system involvement, renal impairment, and microangiopathic hemolytic anemia. Timely initiation of eculizumab therapy resulted in successful disease remission. Further genetic analysis revealed a likely rare pathogenic MCP gene variant.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2157-6998
2157-7005
Relation: https://doaj.org/toc/2157-6998; https://doaj.org/toc/2157-7005
DOI: 10.1055/a-2164-8438
Access URL: https://doaj.org/article/3174f61c57b24856bacdbeb50b432447
Accession Number: edsdoj.3174f61c57b24856bacdbeb50b432447
Database: Directory of Open Access Journals
More Details
ISSN:21576998
21577005
DOI:10.1055/a-2164-8438
Published in:American Journal of Perinatology Reports
Language:English