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自身免疫性溶血性贫血合并巨细胞肝炎:病例报告及文献复习

Autoimmune hemolytic anemia with giant cell hepatitis: case report and review of the literature.

作者信息

Gorelik Mark, Debski Robert, Frangoul Haydar

机构信息

Department of Pediatric Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

出版信息

J Pediatr Hematol Oncol. 2004 Dec;26(12):837-9.

PMID:15591908
Abstract

Autoimmune hemolytic anemia (AIHA) with giant cell hepatitis (GCH) is an uncommon disease in children and is associated with an aggressive and often fatal course. The authors describe a 4-month-old girl who presented with AIHA and elevated liver enzymes. A liver biopsy was consistent with GCH. She was successfully treated with anti-CD20 antibody (rituximab)-containing therapy after failing initial immune suppression therapy. The authors also review the literature for similar cases.

摘要

自身免疫性溶血性贫血(AIHA)合并巨细胞性肝炎(GCH)在儿童中是一种罕见疾病,且病程凶险,常可致命。作者描述了一名4个月大的女童,她患有自身免疫性溶血性贫血且肝酶升高。肝脏活检结果符合巨细胞性肝炎。在初始免疫抑制治疗失败后,她接受了含抗CD20抗体(利妥昔单抗)的治疗并获得成功。作者还回顾了相关类似病例的文献。

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引用本文的文献

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World J Clin Cases. 2021 Sep 6;9(25):7527-7534. doi: 10.12998/wjcc.v9.i25.7527.
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Infantile giant cell hepatitis with autoimmune hemolytic anemia.伴有自身免疫性溶血性贫血的婴儿巨细胞肝炎
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