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移植后爱泼斯坦-巴尔病毒感染及相关淋巴增殖综合征的发生率及其在儿童中的表现。

The frequency of Epstein-Barr virus infection and associated lymphoproliferative syndrome after transplantation and its manifestations in children.

作者信息

Ho M, Jaffe R, Miller G, Breinig M K, Dummer J S, Makowka L, Atchison R W, Karrer F, Nalesnik M A, Starzl T E

机构信息

Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261.

出版信息

Transplantation. 1988 Apr;45(4):719-27. doi: 10.1097/00007890-198804000-00011.

Abstract

Twenty cases of Epstein-Barr virus (EBV)-associated lymphoproliferative syndrome (LPS), defined by the presence of EBV nuclear antigen and/or EBV DNA in tissues, were diagnosed in 1467 transplant recipients in Pittsburgh from 1981-1985. The frequency of occurrence in pediatric transplant recipients was 4% (10/253), while in adults it was 0.8% (10/1214) (P less than .0005). The frequency of LPS in adults declined after 1983 coincidental with the introduction of cyclosporine monitoring. However there was no apparent decline of LPS in children. We describe these ten pediatric cases and one additional case of LPS in a child who received her transplant before 1981. The frequency of EBV infection in 92 pediatric liver recipients was 63%. Of these subjects, 49% were seronegative and 77% of those acquired primary infection. Of 11 cases of pediatric EBV-associated LPS, 10 were in children who had primary infection shortly before or after transplantation. These results reinforce the importance of primary EBV infection in producing LPS, which was previously shown in adults. Children are at greater risk because they are more likely to be seronegative for EBV and to acquire primary infection. Three clinical types of LPS were recognized in children. The first (5 cases) was a self-limited mononucleosislike syndrome. The second syndrome (4 cases) began similarly, but then progressed over the next two months to widespread lymphoproliferation in internal organs and death. The third type (2 cases) was an extranodal intestinal monoclonal B cell lymphoma, occurring late after primary infection.

摘要

1981年至1985年期间,在匹兹堡的1467名移植受者中诊断出20例爱泼斯坦-巴尔病毒(EBV)相关淋巴增殖综合征(LPS),其定义为组织中存在EBV核抗原和/或EBV DNA。小儿移植受者的发病率为4%(10/253),而成人的发病率为0.8%(10/1214)(P<0.0005)。1983年后,随着环孢素监测的引入,成人LPS的发病率有所下降。然而,儿童LPS的发病率并没有明显下降。我们描述了这10例小儿病例以及1例1981年前接受移植的儿童LPS病例。92名小儿肝移植受者中EBV感染率为63%。在这些受试者中,49%为血清阴性,其中77%获得原发性感染。在11例小儿EBV相关LPS病例中,10例是在移植前后不久发生原发性感染的儿童。这些结果强化了原发性EBV感染在引发LPS中的重要性,这一点先前在成人中已得到证实。儿童面临的风险更大,因为他们更有可能EBV血清阴性并获得原发性感染。在儿童中识别出三种临床类型的LPS。第一种(共5例)是自限性单核细胞增多症样综合征。第二种综合征(共4例)起病相似,但在接下来的两个月内进展为内脏广泛淋巴增殖并死亡。第三种类型(共2例)是结外肠道单克隆B细胞淋巴瘤,发生在原发性感染后期。

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