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一名患有乙型肝炎和原发性血色素沉着症的肝移植受者在肝移植后淋巴瘤迅速发展。

Rapid development of lymphoma following liver transplantation in a recipient with hepatitis B and primary hemochromatosis.

作者信息

Palazzo J P, Lundquist K, Mitchell D, Mittal K R, Hann H W, Munoz S, Moritz M J, Jacobs J M, Martin P

机构信息

Department of Pathology, Jefferson Medical School, Philadelphia, Pennsylvania.

出版信息

Am J Gastroenterol. 1993 Jan;88(1):102-4.

PMID:8380533
Abstract

We report a case of a posttransplant lymphoproliferative disorder (PTLD) which presented in a liver allograft shortly after transplantation. The patient, who had been transplanted because of cirrhosis due to primary hemochromatosis and chronic hepatitis B infection (HBV), developed early recurrent HBV in the graft, and 2 months after transplantation, liver biopsies showed a malignant large-cell lymphoma. The neoplastic cells demonstrated Epstein-Barr virus DNA by in situ hybridization. The patient died 3.5 months posttransplant due to liver failure. At autopsy, the liver showed nodules of malignant lymphoma, massive hepatic necrosis, and iron overload, but no evidence of rejection. This report suggests that the grafted liver can be the site of PTLD in recurrent HBV and hemochromatosis.

摘要

我们报告一例移植后淋巴细胞增生性疾病(PTLD),该疾病在肝移植后不久出现在移植肝中。该患者因原发性血色素沉着症和慢性乙型肝炎病毒(HBV)感染导致肝硬化而接受移植,移植肝中早期出现HBV复发,移植后2个月,肝脏活检显示为恶性大细胞淋巴瘤。肿瘤细胞通过原位杂交显示有爱泼斯坦-巴尔病毒DNA。患者在移植后3.5个月因肝衰竭死亡。尸检时,肝脏显示有恶性淋巴瘤结节、大量肝坏死和铁过载,但无排斥反应迹象。本报告提示,在HBV复发和血色素沉着症患者中,移植肝可能是PTLD的发病部位。

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