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儿童再生障碍性贫血肝移植治疗非病毒性肝炎的管理:法国调查。

Management of childhood aplastic anemia following liver transplantation for nonviral hepatitis: A French survey.

机构信息

Department of Pediatric Hematology and Oncology, University Hospital of Caen, Caen, France.

Department of Pediatric Hepatology, AP-HP, Kremlin-Bicêtre Hospital, Le Kremlin-Bicêtre, France.

出版信息

Pediatr Blood Cancer. 2020 Apr;67(4):e28177. doi: 10.1002/pbc.28177. Epub 2020 Jan 11.

Abstract

BACKGROUND

Hepatitis-associated aplastic anemia (AA) is a rare syndrome combining acute hepatitis of variable severity and AA. Hepatitis may be severe enough to require urgent liver transplantation (LT). Herein, we describe clinical presentation and management of a cohort of pediatric patients diagnosed with AA after undergoing LT for nonviral hepatitis.

METHODS

To describe this rare clinical situation, we performed a national survey and identified nine children treated for AA following LT during the last 10 years in France.

RESULTS

All patients were treated first for hepatic failure with urgent LT. AA was diagnosed with a median delay of 34 days [21-200] from the diagnosis of hepatitis. Seven children were treated with antithymocyte globulin/cyclosporine, one with CSA alone and one received bone marrow transplantation. At the last visit (median follow-up: 4 years), outcomes were excellent: all patients were alive and in hematological remission (complete remission: 7; partial remission: 2). Immunosuppressive therapy was pursued in all patients due to the liver transplant. No unusual toxicities were reported.

CONCLUSION

AA after LT is considered a therapeutic challenge. Nevertheless, hematological outcome is good using a standard immunosuppressive approach.

摘要

背景

肝炎相关性再生障碍性贫血(AA)是一种罕见的综合征,其特征为急性肝炎的严重程度不一,同时合并 AA。肝炎的严重程度可能足以需要紧急进行肝移植(LT)。在此,我们描述了一组在接受非病毒性肝炎 LT 后诊断为 AA 的儿科患者的临床表现和治疗。

方法

为了描述这种罕见的临床情况,我们进行了一项全国性调查,在法国确定了过去 10 年中因非病毒性肝炎接受 LT 治疗后出现 AA 的 9 名儿童。

结果

所有患者均首先因肝衰竭接受紧急 LT 治疗。AA 的诊断与肝炎的诊断平均延迟 34 天[21-200]。7 名儿童接受抗胸腺细胞球蛋白/环孢素治疗,1 名儿童单独接受 CSA 治疗,1 名儿童接受骨髓移植。在最后一次就诊(中位随访时间:4 年)时,结果均良好:所有患者均存活且处于血液学缓解(完全缓解:7 例;部分缓解:2 例)。由于肝移植,所有患者均继续接受免疫抑制治疗。未报告任何异常毒性。

结论

LT 后发生的 AA 被认为是一种治疗挑战。然而,采用标准的免疫抑制方法,血液学结局良好。

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