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患有爱泼斯坦-巴尔病毒血症和移植后淋巴细胞增生性疾病的小儿肝移植患者的移植物排斥反应。

Graft rejection in pediatric liver transplant patients with Epstein-Barr viremia and post-transplant lymphoproliferative disease.

作者信息

Weiner Chana, Weintraub Lauren, Wistinghausen Birte, Tomaino Juli, Arnon Ronen, Kerkar Nanda, Miloh Tamir

机构信息

Department of Pediatrics, Mount Sinai Medical Center, New York, NY, USA.

出版信息

Pediatr Transplant. 2012 Aug;16(5):458-64. doi: 10.1111/j.1399-3046.2012.01713.x. Epub 2012 May 4.

DOI:10.1111/j.1399-3046.2012.01713.x
PMID:22554096
Abstract

Treatment of primary EV and PTLD in pediatric LT recipients (pLT) involves IS reduction/cessation. Retrospective review of pLT at our institution from 2001-2009 was conducted to characterize risk factors for GR after EV/ PTLD. Of 184 pLT, EV occurred in 61 (33%) at mean 16.5 m (0-82) and PTLD in 18 (9.8%) at mean 17.7 m (3-78) post-LT. Median age at pLT was 11 m (1-245 m) and follow-up six yr. For EV, 86% underwent IS reduction and 51% received antivirals. GR occurred in 12 (27.9%) with EV and 15 (83.3%) after PTLD diagnosis (relative risk of GR for PTLD 2.98). GR treated with methylprednisolone bolus in half and/or oral IS in half. Following GR therapy, four had PTLD relapses, no graft loss and one EV patient required re-transplantation. GR history before EV was a risk factor for GR after EV (p = 0.024). GR at any point after pLT was a risk factor for PTLD (p = 0.001). Children with EV and GR prior to EV should be monitored closely for GR after IS reduction and GR is a significant risk factor for PTLD. Most children with PTLD eventually developed GR.

摘要

小儿肝移植(pLT)受者原发性EB病毒(EV)感染和移植后淋巴增殖性疾病(PTLD)的治疗包括减少或停用免疫抑制剂(IS)。我们对本机构2001年至2009年的pLT进行了回顾性研究,以确定EV/PTLD后发生移植物排斥(GR)的危险因素。184例pLT中,61例(33%)发生EV,平均时间为肝移植后16.5个月(0 - 82个月);18例(9.8%)发生PTLD,平均时间为肝移植后17.7个月(3 - 78个月)。pLT时的中位年龄为11个月(1 - 245个月),随访6年。对于EV,86%的患者减少了IS用量,51%的患者接受了抗病毒治疗。12例(27.9%)EV患者发生GR,15例(83.3%)在诊断PTLD后发生GR(PTLD发生GR的相对风险为2.98)。一半的GR患者接受了甲泼尼龙冲击治疗,另一半接受了口服IS治疗。GR治疗后,4例发生PTLD复发,无移植物丢失,1例EV患者需要再次移植。EV发生前有GR病史是EV后发生GR的危险因素(p = 0.024)。pLT后任何时间发生GR是PTLD的危险因素(p = 0.001)。EV患者且在EV前发生GR的儿童在减少IS用量后应密切监测GR情况,GR是PTLD的重要危险因素。大多数PTLD患儿最终发生了GR。

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