Liver Transplantation Center, National Clinical Research Center for Digestive Diseases, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Intensive Care Unit, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Int J Clin Pract. 2021 Apr;75(4):e13843. doi: 10.1111/ijcp.13843. Epub 2020 Dec 14.
The purpose of this study was to analyse the clinical and pathological characteristics, treatments and outcomes of post-transplant lymphoproliferative disorder (PTLD) in paediatric liver transplant recipients.
A retrospective analysis of records from nine paediatric liver transplant recipients with PTLD who were treated at our Liver Transplant Center over the period from June 2013 to August 2018.
Of these nine patients, seven received liver transplantation in our centre and the remaining two patients at other hospitals. The overall incidence of PTLD in paediatric liver transplant recipients in our centre was 1.4% (7/485). The median onset of PTLD after liver transplantation was 11 months. Three cases were classified as infectious mononucleosis PTLD, one case was plasmacytic hyperplasia PTLD, one case was polymorphic PTLD and two cases were Burkitt lymphoma. One case showed diffuse large B-cell lymphoma and one was classical Hodgkin lymphoma-like PTLD. These patients presented with different clinical manifestations including fever, anaemia, diarrhoea, hypoproteinaemia, enlargement of lymph nodes, hepatosplenomegaly, jaundice, bowel obstruction and even intestinal perforation. Nine patients were positive for EBV-DNA in serum. After diagnosis, immunosuppressants were reduced or discontinued in all cases. Eight patients received anti-CD20 monoclonal antibody (Rituximab) therapy, four cases were treated with a combination of chemotherapy (R-CHOP, ABVD, COPP/ABV) and one case was combined with radiotherapy. Two cases received surgical treatment due to bowel obstruction. Eight of these patients achieved a complete remission and remained healthy when assessed at the time of final follow-up. One patient died as a result of PTLD progression.
PTLD is one of the most serious and fatal complications after liver transplantation. The definitive diagnosis requires histopathology. Treatment varies and basically includes immunosuppression reduction, anti-CD20 antibody, surgery, radiotherapy and chemotherapy.
本研究旨在分析儿童肝移植受者移植后淋巴组织增生性疾病(PTLD)的临床和病理特征、治疗方法和结局。
回顾性分析 2013 年 6 月至 2018 年 8 月在我院肝脏移植中心接受治疗的 9 例 PTLD 儿童肝移植受者的病历资料。
9 例患者中,7 例在我院行肝移植,其余 2 例在其他医院行肝移植。我院儿童肝移植受者 PTLD 的总发生率为 1.4%(7/485)。PTLD 肝移植后中位发病时间为 11 个月。3 例为传染性单核细胞增多症样 PTLD,1 例为浆细胞增生性 PTLD,1 例为多形性 PTLD,2 例为伯基特淋巴瘤。1 例为弥漫性大 B 细胞淋巴瘤,1 例为经典霍奇金淋巴瘤样 PTLD。这些患者表现出不同的临床表现,包括发热、贫血、腹泻、低蛋白血症、淋巴结肿大、肝脾肿大、黄疸、肠梗阻,甚至肠穿孔。9 例患者血清 EBV-DNA 阳性。诊断后,所有患者均减少或停用免疫抑制剂。8 例患者接受抗 CD20 单克隆抗体(利妥昔单抗)治疗,4 例患者接受化疗(R-CHOP、ABVD、COPP/ABV)联合治疗,1 例患者联合放疗。2 例患者因肠梗阻行手术治疗。8 例患者完全缓解,在最终随访时健康状况良好。1 例患者因 PTLD 进展死亡。
PTLD 是肝移植后最严重和致命的并发症之一。明确诊断需要组织病理学。治疗方法多种多样,基本包括减少免疫抑制、抗 CD20 抗体、手术、放疗和化疗。