Niedermeier Dawn M, Frei-Lahr Debra A, Hall Philip D
Department of Pharmacy Services, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Pharmacotherapy. 2005 Aug;25(8):1134-40. doi: 10.1592/phco.2005.25.8.1134.
Fortunately, the occurrence of acute myeloid leukemia (AML) during pregnancy is rare. We report a case of successful fetal outcome with standard induction and consolidation treatment in the second and third trimesters, respectively. A 37-year-old woman in her second trimester (21 wks) of pregnancy was found to have acute myeloid leukemia. She elected to maintain the pregnancy and underwent induction with cytarabine and idarubicin. Her hospital course was complicated by Pseudomonas vesicularis and gram-positive bacilli (not Bacillus anthracis) septicemia, but she obtained complete remission. After discharge, a fetal echocardiogram at 26 weeks revealed a mildly dilated right ventricle with mild systolic dysfunction, and the left ventricle appeared smaller than normal with mild systolic dysfunction. The patient then received consolidation therapy with high-dose cytarabine. On day 14 of consolidation, filgrastim 16 mug/kg was added to improve stem cell mobilization. A total of 19.8x10(6) CD34+ cells/kg were collected with a single apheresis session. At 37 weeks, she delivered a viable female infant weighing 3 lbs 12 oz. Fetal abnormalities included acrocyanosis, shallow sacral dimple, short digits and limbs, and prominent frontal skull with mild macrognathia. A postnatal echocardiogram revealed a moderate-sized membranous ventricular septal defect. The ventricular septal defect proved significant and required surgical repair at 5 months. Approximately 4 weeks after delivery, the mother underwent autologous peripheral stem cell transplantation. Unfortunately, 100 days after transplantation, she had a relapse of AML. After a brief remission from a second induction, the patient died.
幸运的是,孕期急性髓系白血病(AML)的发生率很低。我们报告一例病例,患者分别在孕中期和孕晚期接受标准诱导和巩固治疗,胎儿结局良好。一名37岁处于孕中期(21周)的女性被诊断为急性髓系白血病。她选择继续妊娠,并接受了阿糖胞苷和伊达比星诱导治疗。她的住院过程因水泡假单胞菌和革兰氏阳性杆菌(非炭疽芽孢杆菌)败血症而复杂化,但她获得了完全缓解。出院后,26周时的胎儿超声心动图显示右心室轻度扩张,伴有轻度收缩功能障碍,左心室似乎比正常小,伴有轻度收缩功能障碍。然后患者接受了大剂量阿糖胞苷巩固治疗。在巩固治疗的第14天,添加了16微克/千克的非格司亭以改善干细胞动员。通过单次单采采集了总共19.8×10⁶个CD34⁺细胞/千克。37周时,她产下一名体重3磅12盎司的存活女婴。胎儿异常包括肢端青紫、骶部浅凹、指(趾)和肢体短小以及额骨突出伴轻度巨颌。产后超声心动图显示有一个中等大小的膜周室间隔缺损。该室间隔缺损被证明很严重,在5个月时需要手术修复。分娩后约4周,母亲接受了自体外周干细胞移植。不幸的是,移植后100天,她的AML复发。在第二次诱导治疗后短暂缓解后,患者死亡。