Amankwah K S, Dick B W, Dodge S
Obstet Gynecol. 1980 Mar;55(3 Suppl):42S-44S. doi: 10.1097/00006250-198003001-00013.
Hemolytic anemia due to deficiency of erythrocytic pyruvate kinase is a rare autosomal recessive disorder. Pregnancy complicated by pyruvate kinase deficiency is rare; there are only 8 reported cases in the literature. A case is described that was characterized by increased hemolysis during pregnancy, requiring blood transfusions before and after delivery, and complicated by severe preeclampsia at term. Fetal and maternal outcome was successful. Increased hemolysis and favorable perinatal outcome occurred in all 8 reported cases.
由于红细胞丙酮酸激酶缺乏所致的溶血性贫血是一种罕见的常染色体隐性疾病。妊娠合并丙酮酸激酶缺乏症很罕见;文献中仅报道了8例。本文描述了1例病例,其特点是孕期溶血增加,分娩前后均需输血,且足月时并发严重先兆子痫。胎儿和母亲结局良好。在所有8例报道的病例中均出现了溶血增加及良好的围产期结局。