Ashihara E, Shimazaki C, Hirata T, Okawa K, Oku N, Goto H, Inaba T, Fujita N, Nakagawa M
Second Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
Bone Marrow Transplant. 1993 Sep;12(3):297-9.
A 22-year-old woman diagnosed as AML (M3) received myeloablative chemotherapy followed by autologous peripheral stem cell transplantation (PBSCT). Rapid hematopoietic reconstitution occurred. By day 10, the neutrophil count was > 0.5 x 10(9)/l and the platelet count > 50 x 10(9)/l. The platelet count was 145 x 10(9)/l on day 20. Purpura developed on the anterior chest and legs on day 50, at which time the platelet count fell to 17 x 10(9)/l. The BM was hypocellular with an increase in megakaryocytes. Platelet-associated IgG (PAIgG) was 88.1 ng/10(7) platelets (normal range 9-25 ng/10(7)); a diagnosis of idiopathic thrombocytopenic purpura (ITP) was made. Prednisolone administration led to an increase in the platelet count and a decrease in PAIgG. Analysis of lymphocyte subsets revealed an increased number of CD3+ gamma/delta T cells. It is postulated that the thrombocytopenia in this case was due to an autoimmune mechanism such as ITP.
一名被诊断为急性髓系白血病(M3型)的22岁女性接受了清髓性化疗,随后进行了自体外周血干细胞移植(PBSCT)。造血功能迅速恢复。到第10天时,中性粒细胞计数>0.5×10⁹/L,血小板计数>50×10⁹/L。第20天时血小板计数为145×10⁹/L。第50天时前胸和腿部出现紫癜,此时血小板计数降至17×10⁹/L。骨髓细胞减少,巨核细胞增多。血小板相关IgG(PAIgG)为88.1 ng/10⁷血小板(正常范围9 - 25 ng/10⁷);诊断为特发性血小板减少性紫癜(ITP)。给予泼尼松龙后血小板计数升高,PAIgG降低。淋巴细胞亚群分析显示CD3⁺γ/δT细胞数量增加。推测该病例中的血小板减少是由于ITP等自身免疫机制所致。