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孕妇β-中间型地中海贫血发生迟发性重度溶血性输血反应:使用依库珠单抗治疗后的成功结局。

Delayed Severe Hemolytic Transfusion Reaction During Pregnancy in a Woman with β-Thalassemia Intermediate: Successful Outcome After Eculizumab Administration.

机构信息

Department of Internal Medicine, Lyon Civil Hospices, Edouard Herriot Hospital, Lyon, France.

French Blood Establishment Auvergne-Rhône-Alpes, Croix-Rousse Hospital, Lyon, France.

出版信息

Am J Case Rep. 2021 May 13;22:e931107. doi: 10.12659/AJCR.931107.

Abstract

BACKGROUND Delayed hemolytic transfusion reactions (DHTR) are life-threatening complications mostly triggered by red blood cell (RBC) transfusions in patients with hemoglobinopathy. CASE REPORT We present a case of DHTR and hyperhemolysis syndrome in a 39-year-old pregnant woman with a history of ß-thalassemia intermediate in whom the hemoglobin (Hb) level fell to 27 g/L after transfusion of 2 units of crossmatch-compatible packed RBCs. No allo- or auto-antibody formation was detected. Administration of intravenous immunoglobulins and methylprednisolone followed by anti-CD20 rituximab was tried, but was unsuccessful. Infusions of eculizumab (900 mg twice at a 7-day interval) followed by another course of intravenous immunoglobulins (2 g/kg/day for 5 days) and combined with repeated erythropoietin injections (darbepoetin alpha 300 µg/week) finally allowed biological and clinical improvement. Blood counts remained controlled until delivery. Despite signs of intrauterine growth retardation, she gave birth by cesarean section at 31 weeks of pregnancy to a 1.15-kg infant. CONCLUSIONS Eculizumab seems to be of benefit in DHTR associated with hyperhemolysis and should be used early in the treatment of this pathology. Despite premature birth, our case report showed an acceptable outcome for the infant when eculizumab treatment was used during pregnancy.

摘要

背景

迟发性溶血性输血反应(DHTR)是一种危及生命的并发症,主要由血红蛋白病患者输注红细胞(RBC)引发。

病例报告

我们报告了一例 39 岁妊娠合并中间型β地中海贫血患者的 DHTR 和高溶血性综合征病例,该患者输注 2 单位交叉配型相合的浓缩 RBC 后血红蛋白(Hb)水平降至 27 g/L。未检测到同种异体或自身抗体形成。尝试给予静脉注射免疫球蛋白和甲基强的松龙,随后给予抗 CD20 利妥昔单抗,但均无效。给予依库珠单抗(900 mg,7 天间隔 2 次)输注,随后给予另一疗程静脉注射免疫球蛋白(2 g/kg/天,5 天),并结合重复红细胞生成素注射(达贝泊汀α 300 μg/周),最终使患者的生物学和临床状况得到改善。血液计数一直得到控制,直至分娩。尽管有宫内生长迟缓的迹象,她仍在妊娠 31 周时通过剖宫产分娩出 1.15 公斤的婴儿。

结论

依库珠单抗似乎对高溶血性DHTR 有益,应在该病理的治疗早期使用。尽管早产,我们的病例报告显示,在妊娠期间使用依库珠单抗治疗时,婴儿的结局是可以接受的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/8130975/245ab44dd3e2/amjcaserep-22-e931107-g001.jpg

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