Advani Sonali D, Nellore Anoma, Hadjivassiliou Giorgos, Eckhoff Devin E, Salzman Donna, Lavie Daniel, Pavlidakey Peter, Baddley John W
1 Section of Infectious Diseases, Yale School of Medicine, New Haven, CT, USA.
2 Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL, USA.
Prog Transplant. 2018 Sep;28(3):267-270. doi: 10.1177/1526924818781558. Epub 2018 Jun 28.
Graft-versus-host disease (GvHD) is a rare but fatal complication after solid organ transplantation arising in 1% to 2% of cases. We report 2 cases of GvHD after orthotopic liver transplantation. Both patients had a history of hepatitis C virus (HCV) infection prior to transplantation. Both cases presented between 1 and 4 months after transplantation with rash, pancytopenia, and/or diarrhea. Our second case also developed oral and ocular manifestations after liver transplantation, which are more commonly described after stem cell transplantation. Diagnosis in both cases was made by clinical presentation in conjunction with histopathology and flow cytometry. Both patients were treated by increasing immunosuppression with tacrolimus and high-dose steroids. Response to treatment differed based on the degree of pancytopenia. Our case report is distinguished by several factors such as the context of GvHD presentation and the role of HCV treatment. Diagnosis of GvHD is difficult and often delayed due to nonspecific presentation that overlaps with other conditions. Furthermore, the relation between HCV treatment and potential initiation of GvHD in solid organ transplant patients is unclear.
移植物抗宿主病(GvHD)是实体器官移植后一种罕见但致命的并发症,发生率为1%至2%。我们报告2例原位肝移植后发生GvHD的病例。两名患者在移植前均有丙型肝炎病毒(HCV)感染史。两例均在移植后1至4个月出现皮疹、全血细胞减少和/或腹泻。我们的第二例患者在肝移植后还出现了口腔和眼部表现,这些表现更常见于干细胞移植后。两例均通过临床表现结合组织病理学和流式细胞术进行诊断。两名患者均通过增加他克莫司免疫抑制和大剂量类固醇进行治疗。治疗反应因全血细胞减少的程度而异。我们的病例报告因GvHD表现的背景以及HCV治疗的作用等几个因素而有所不同。由于与其他病症重叠的非特异性表现,GvHD的诊断很困难且常常延迟。此外,实体器官移植患者中HCV治疗与GvHD潜在发生之间的关系尚不清楚。