Omata F, Ueno F, Kushibiki Y, Takahashi H
Department of Medicine, Tokai University School of Medicine, Kanagawa, Japan.
J Gastroenterol. 1994 Oct;29(5):653-5. doi: 10.1007/BF02365451.
A 19-year-old male healthy hepatitis B virus (HBV) carrier developed fulminant hepatitis following allogenic bone marrow transplantation (BMT) from his brother, who was also a healthy HBV carrier, during the first complete remission of acute myelogenic leukemia (M1, FAB classification). Serum markers related to both HBV and hepatitis C virus (HCV) were elevated during active liver injury when a point mutation in the precore (pre-C) region occurred in the HBV. The patient received low-dose interferon alpha (IFN-alpha), while the dose of cyclosporin A was tapered; the patient eventually recovered from the liver injury. Fulminant hepatitis due to HBV and/or HCV following BMT is rare, and it is considered to have a very poor prognosis. The rationale for the use of low-dose IFN-alpha with cyclosporin A (CyA) is discussed.
一名19岁的健康乙型肝炎病毒(HBV)携带者,在急性髓性白血病(M1,FAB分类)首次完全缓解期接受了来自其同样为健康HBV携带者的兄弟的异基因骨髓移植(BMT)后,发生了暴发性肝炎。在肝脏损伤活动期,当HBV前核心(pre-C)区出现点突变时,与HBV和丙型肝炎病毒(HCV)相关的血清标志物均升高。患者接受了小剂量的α干扰素(IFN-α)治疗,同时逐渐减少环孢素A的剂量;患者最终从肝损伤中康复。BMT后由HBV和/或HCV引起的暴发性肝炎很少见,且被认为预后很差。本文讨论了联合使用小剂量IFN-α和环孢素A(CyA)的理论依据。