Gondo H, Hamasaki Y, Nakayama H, Kondo T, Mitsuuchi J, Kawaga Y, Taniguchi S, Harada M, Niho Y
Division of Internal Medicine, Sanshinkai Hara Hospital, Fukuoka, Japan.
Acta Haematol. 1990;83(3):140-4. doi: 10.1159/000205191.
A 29-year-old female in the 20th week of pregnancy was admitted because of a change in the ABO blood group and bleeding tendency. Acute myelogenous leukemia was diagnosed with a weak reaction of red blood cells with anti-A antibody and a decreased level of A-transferase activity. Though the patient tolerated intensive chemotherapy and achieved complete remission, thrombocytopenia persisted after consolidation chemotherapy. Since platelet-associated IgG was elevated, thrombocytopenia was considered to be immune-mediated. In the third trimester, premature separation of the normally implanted placenta developed and cesarean section was performed. The male baby was also thrombocytopenic, but successfully treated with gamma-globulin.
一名怀孕20周的29岁女性因ABO血型改变和出血倾向入院。诊断为急性髓系白血病,其红细胞与抗A抗体反应较弱,A转移酶活性水平降低。尽管患者耐受了强化化疗并实现了完全缓解,但巩固化疗后血小板减少症仍持续存在。由于血小板相关IgG升高,血小板减少症被认为是免疫介导的。在孕晚期,发生了正常着床胎盘的早剥,并进行了剖宫产。男婴也患有血小板减少症,但通过静脉注射丙种球蛋白成功治愈。