{"title":"抗M同种免疫导致的严重胎儿溶血病:病例报告和文献","authors":"Fatemeh Golshahi , Fatemeh Rahimi Sharbaf , Mahboobeh Shirazi , Behrokh Sahebdel , Jafar Golshahi , Simon Dadoun , Soroush Aalipour , Mohammad Haddadi","doi":"10.1016/j.crwh.2024.e00620","DOIUrl":null,"url":null,"abstract":"<div><p>Fetal hemolysis is caused by maternal antibodies that cross the placenta. Anti-M antibodies can rarely cause severe forms of alloimmunization in the fetus and newborn. We present a case of severe anti-M alloimmunization requiring a total of 8 intrauterine transfusions, in a patient with a prior poor obstetrical history. A 35-year-old Iranian pregnant woman with a prior obstetrical history of one abortion and two stillbirths was found to have had anti-M antibody titers 1:8 and accompanying elevated middle cerebral artery peak systolic velocity (MCA-PSV) of 1.9 MoM suggestive of severe fetal anemia at 17 weeks of gestation. Persistently elevated fetal MCA-PSV was noted despite intraperitoneal transfusion at 17, 19, and 22 weeks. Fetal blood sampling at 27 weeks confirmed severe fetal anemia (3 g/dL), which required additional intravascular and intraperitoneal blood transfusion. At 37 weeks, elective cesarean section was performed. Neonatal hemoglobin immediately after delivery was 10.1 g/dL. In addition to standard supportive care, the neonate required two additional transfusions and remained in the neonatal intensive care unit (NICU) for 23 days.</p><p>Anti-M antibodies are a rare cause of severe alloimmunization. We present a case in order to improve management.</p></div>","PeriodicalId":9657,"journal":{"name":"Case Reports in Women's Health","volume":"42 ","pages":"Article e00620"},"PeriodicalIF":0.7000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214911224000419/pdfft?md5=b994db6417134720cd20da425631447a&pid=1-s2.0-S2214911224000419-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Severe fetal hemolytic disease due to anti-M alloimmunization: A case report and literature review\",\"authors\":\"Fatemeh Golshahi , Fatemeh Rahimi Sharbaf , Mahboobeh Shirazi , Behrokh Sahebdel , Jafar Golshahi , Simon Dadoun , Soroush Aalipour , Mohammad Haddadi\",\"doi\":\"10.1016/j.crwh.2024.e00620\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Fetal hemolysis is caused by maternal antibodies that cross the placenta. Anti-M antibodies can rarely cause severe forms of alloimmunization in the fetus and newborn. We present a case of severe anti-M alloimmunization requiring a total of 8 intrauterine transfusions, in a patient with a prior poor obstetrical history. A 35-year-old Iranian pregnant woman with a prior obstetrical history of one abortion and two stillbirths was found to have had anti-M antibody titers 1:8 and accompanying elevated middle cerebral artery peak systolic velocity (MCA-PSV) of 1.9 MoM suggestive of severe fetal anemia at 17 weeks of gestation. Persistently elevated fetal MCA-PSV was noted despite intraperitoneal transfusion at 17, 19, and 22 weeks. Fetal blood sampling at 27 weeks confirmed severe fetal anemia (3 g/dL), which required additional intravascular and intraperitoneal blood transfusion. At 37 weeks, elective cesarean section was performed. Neonatal hemoglobin immediately after delivery was 10.1 g/dL. In addition to standard supportive care, the neonate required two additional transfusions and remained in the neonatal intensive care unit (NICU) for 23 days.</p><p>Anti-M antibodies are a rare cause of severe alloimmunization. We present a case in order to improve management.</p></div>\",\"PeriodicalId\":9657,\"journal\":{\"name\":\"Case Reports in Women's Health\",\"volume\":\"42 \",\"pages\":\"Article e00620\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2214911224000419/pdfft?md5=b994db6417134720cd20da425631447a&pid=1-s2.0-S2214911224000419-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Case Reports in Women's Health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214911224000419\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Women's Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214911224000419","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
胎儿溶血是由穿过胎盘的母体抗体引起的。抗 M 抗体很少会导致胎儿和新生儿出现严重的同种免疫。我们介绍了一例严重的抗M抗体同种免疫病例,患者曾有不良的产科病史,总共需要进行8次宫内输血。一名 35 岁的伊朗孕妇曾有过一次流产和两次死胎的产科病史,她在妊娠 17 周时发现抗 M 抗体滴度为 1:8,并伴有大脑中动脉峰值收缩速度(MCA-PSV)升高至 1.9 MoM,提示胎儿严重贫血。尽管在 17、19 和 22 周进行了腹腔输血,但胎儿 MCA-PSV 仍持续升高。27 周时的胎儿抽血证实胎儿严重贫血(3 g/dL),需要进行额外的血管内和腹腔内输血。37 周时,进行了选择性剖宫产。产后新生儿血红蛋白为 10.1 g/dL。除了标准的支持治疗外,新生儿还需要两次额外的输血,并在新生儿重症监护室(NICU)待了23天。抗 M 抗体是导致严重同种免疫的罕见原因,我们介绍了一个病例,以改善管理。
Severe fetal hemolytic disease due to anti-M alloimmunization: A case report and literature review
Fetal hemolysis is caused by maternal antibodies that cross the placenta. Anti-M antibodies can rarely cause severe forms of alloimmunization in the fetus and newborn. We present a case of severe anti-M alloimmunization requiring a total of 8 intrauterine transfusions, in a patient with a prior poor obstetrical history. A 35-year-old Iranian pregnant woman with a prior obstetrical history of one abortion and two stillbirths was found to have had anti-M antibody titers 1:8 and accompanying elevated middle cerebral artery peak systolic velocity (MCA-PSV) of 1.9 MoM suggestive of severe fetal anemia at 17 weeks of gestation. Persistently elevated fetal MCA-PSV was noted despite intraperitoneal transfusion at 17, 19, and 22 weeks. Fetal blood sampling at 27 weeks confirmed severe fetal anemia (3 g/dL), which required additional intravascular and intraperitoneal blood transfusion. At 37 weeks, elective cesarean section was performed. Neonatal hemoglobin immediately after delivery was 10.1 g/dL. In addition to standard supportive care, the neonate required two additional transfusions and remained in the neonatal intensive care unit (NICU) for 23 days.
Anti-M antibodies are a rare cause of severe alloimmunization. We present a case in order to improve management.