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一名ABO血型不相容肾移植受者发生的快速进展性肝泡型包虫病。

Rapidly progressive hepatic alveolar echinococcosis in an ABO-incompatible renal transplant recipient.

作者信息

Geyer M, Wilpert J, Wiech T, Theilacker C, Stubanus M, Kramer-Zucker A, Fischer K-G, Drognitz O, Frydrychowicz A, Kern W, Walz G, Pisarski P

机构信息

Renal Division, University Hospital Freiburg, Freiburg, Germany.

出版信息

Transpl Infect Dis. 2011 Jun;13(3):278-84. doi: 10.1111/j.1399-3062.2010.00583.x. Epub 2010 Oct 26.

Abstract

We report on the case of an ABO-incompatible renal re-transplant recipient maintained on an intensified immunosuppressive regimen for recurrent cellular rejection episodes and transplant glomerulopathy who presented with rapidly growing hepatic tumors, radiologically suggestive of hemangiosarcoma. Upon resection and pathological work-up, the lesions revealed alveolar echinococcosis, a rare but potentially life-threatening parasitosis. Usually infection with Echinococcus multilocularis remains asymptomatic for extended periods of time and can go unrecognized for years. In the case presented, we observed an atypically rapid growth pattern of E. multilocularis that might have been due to the extent of the immunosuppressive regimen, which included repetitive anti-CD20 treatments. Retrospectively performed serological studies with enzyme-linked immunosorbent assays known to provide high sensitivity and specificity for the detection of echinococcosis in the general population, yielded ambiguous results in our immunocompromised host, which could be, in part, explained by B-cell depletion and its effects on antibody production and indirect actions on cellular immunity. In conclusion, this is the first report to our knowledge of hepatic alveolar echinococcosis in a renal transplant recipient. This case documents an altered clinical course of the parasitosis and the challenge of serological diagnostic tools under an intensified regimen of immunosuppressive agents, including rituximab.

摘要

我们报告了一例ABO血型不相容的肾再移植受者的病例,该受者因反复发生细胞排斥反应和移植肾小球病而接受强化免疫抑制方案治疗,出现了快速生长的肝脏肿瘤,影像学检查提示为血管肉瘤。经切除和病理检查,病变显示为肺泡型棘球蚴病,这是一种罕见但可能危及生命的寄生虫病。通常,多房棘球绦虫感染在很长一段时间内无症状,可能多年未被发现。在本病例中,我们观察到多房棘球绦虫的一种非典型快速生长模式,这可能归因于免疫抑制方案的程度,该方案包括重复的抗CD20治疗。回顾性地进行的血清学研究采用了已知对一般人群棘球蚴病检测具有高灵敏度和特异性的酶联免疫吸附测定法,在我们的免疫受损宿主中得出了不明确的结果,这部分可以通过B细胞耗竭及其对抗体产生的影响以及对细胞免疫的间接作用来解释。总之,据我们所知,这是首例肾移植受者发生肝脏肺泡型棘球蚴病的报告。该病例记录了寄生虫病的临床病程改变以及在包括利妥昔单抗在内的强化免疫抑制剂方案下血清学诊断工具面临的挑战。

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