Department of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital, Kobe, Japan.
Transpl Int. 2010 May 1;23(5):e1-4. doi: 10.1111/j.1432-2277.2009.01028.x. Epub 2009 Dec 17.
A 30-year-old woman developed severe liver dysfunction 1 year after bone marrow transplantation (BMT) from an HLA-identical sibling donor for B lymphoblastic leukemia (B-ALL) during the tapering of cyclosporin A. The histologic picture resembled autoimmune hepatitis (AIH), although neither autoantibody nor hypergammaglobulinemia was detected. She entered hepatic coma, and underwent living donor liver transplantation from the same donor on day 421 after BMT. She is well 18 months after the procedure, showing normal liver function and hematopoiesis. AIH-like hepatic graft-versus-host disease (GVHD) has not been documented. This patient is the second case of living donor liver transplantation for hepatic GVHD from the same donor.
一位 30 岁女性在接受 HLA 同基因供体骨髓移植(BMT)治疗 B 淋巴母细胞白血病(B-ALL)后,在环孢素 A 减量过程中 1 年后出现严重肝功能障碍。组织学表现类似于自身免疫性肝炎(AIH),尽管未检测到自身抗体或高球蛋白血症。她出现肝昏迷,并在 BMT 后第 421 天接受同一位供体的活体肝移植。移植后 18 个月,她情况良好,肝功能和造血功能正常。尚未记录到类似 AIH 的肝移植物抗宿主病(GVHD)。该患者是第二例来自同一供体的活体肝移植治疗肝 GVHD 的病例。