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一名肝移植受者发生成人T细胞白血病,在移植物排斥反应发生后病情未进展。

Adult T-cell leukemia in a liver transplant recipient that did not progress after onset of graft rejection.

作者信息

Suzuki Shinsuke, Uozumi Kimiharu, Maeda Masahiko, Yamasuji Yoshiko, Hashimoto Shin-ichi, Komorizono Yasuji, Owatari Satsuki, Tokunaga Masahito, Haraguchi Kouichi, Arima Naomichi

机构信息

Department of Haematology, Kagoshima University Hospital, Kagoshima, Japan.

出版信息

Int J Hematol. 2006 Jun;83(5):429-32. doi: 10.1532/IJH97.05158.

Abstract

A liver allograft recipient developed acute-type adult T-cell leukemia (ATL) during tacrolimus treatment, 2 years after undergoing transplantation for subacute fulminant hepatitis. Both donor and recipient were asymptomatic carriers of human T-cell lymphotropic virus type I (HTLV-I), but the ATL cells originated from the recipient. Tacrolimus treatment was discontinued, and combination chemotherapy was administered. The patient achieved complete remission, but the transplanted liver was acutely and chronically rejected. The patient did not respond to rescue therapy with tacrolimus, prednisolone, and mycophenolate mofetil and died of hepatic failure. Liver biopsies showed CD4+ ATL cell infiltration at the onset of ATL but not at the terminal stage. Moreover, Southern blotting revealed clonal integration of HTLV-I into the host genome of lymphoma cells at onset but not at the terminal stage. ATL after liver transplantation has not been previously described. The clinical course of the posttransplantational ATL was atypical, because it did not progress after the onset of rejection.

摘要

一名肝移植受者在接受亚急性暴发性肝炎移植2年后,于他克莫司治疗期间发生急性成人T细胞白血病(ATL)。供体和受体均为I型人类嗜T细胞病毒(HTLV-I)无症状携带者,但ATL细胞起源于受体。停用他克莫司治疗,并给予联合化疗。患者实现完全缓解,但移植肝发生急性和慢性排斥反应。患者对他克莫司、泼尼松龙和霉酚酸酯的挽救治疗无反应,死于肝衰竭。肝活检显示在ATL发病时存在CD4+ ATL细胞浸润,但在终末期未出现。此外,Southern印迹法显示在发病时HTLV-I克隆整合到淋巴瘤细胞的宿主基因组中,但在终末期未出现。肝移植后发生ATL此前未见报道。移植后ATL的临床病程不典型,因为在排斥反应发生后未进展。

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