伊库利珠单抗
非典型溶血尿毒综合征
血栓性微血管病
怀孕
医学
妊娠期
胎儿
疾病
单克隆
免疫学
补体系统
内科学
单克隆抗体
抗体
生物
遗传学
作者
Gianluigi Ardissino,Manuela Wally Ossola,Giulia Maria Baffero,Angelo Rigotti,Massimo Cugno
标识
DOI:10.1097/aog.0b013e31828e2612
摘要
In Brief BACKGROUND: Atypical hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy often caused by mutations in complement genes. During pregnancy, disease outcome is poor both for mother and fetus. Since 2009, the humanized monoclonal antibody eculizumab has been successfully used in the treatment of atypical HUS in nonpregnant patients. CASE: A 26-year-old woman with a homozygous mutation in complement factor H developed a relapse of atypical HUS at 17 weeks of gestation in her first pregnancy. Because the disease remained active despite multiple plasma exchanges, eculizumab was started at 26 weeks of gestation. It was well tolerated and has led to remission and to the delivery of a healthy neonate. CONCLUSION: Eculizumab may be useful for the treatment of atypical HUS during pregnancy. Eculizumab may be beneficial for the treatment of atypical hemolytic uremic syndrome in pregnancy.
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