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儿童血清阴性自身免疫性肝炎:疾病谱

Seronegative autoimmune hepatitis in children: Spectrum of disorders.

作者信息

Maggiore Giuseppe, Socie Gérard, Sciveres Marco, Roque-Afonso Anne-Marie, Nastasio Silvia, Johanet Catherine, Gottrand Fréderic, Fournier-Favre Sébastien, Jacquemin Emmanuel, Bernard Olivier

机构信息

Dipartimento di Medicina Clinica e Sperimentale, Università di Pisa, Gastroenterologia Pediatrica, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy; Epatologia Pediatrica e Trapianto di fegato, ISMETT, University of Pittsburgh Medical Center, Palermo, Italy.

Hématologie/Greffe de Moelle, INSERM U 1160 AP-HP, Université Paris VII, Hôpital Saint Louis, Paris, France.

出版信息

Dig Liver Dis. 2016 Jul;48(7):785-91. doi: 10.1016/j.dld.2016.03.015. Epub 2016 Mar 28.

Abstract

BACKGROUND

A few children with acute or chronic liver disease display histological features compatible with autoimmune hepatitis, but lack specific serological markers.

AIM

To describe features, management and outcome of childhood seronegative autoimmune hepatitis.

METHODS

From 1988 to 2010, 38 children were included under the following criteria: negative virological studies, no serum autoantibodies, exclusion of other causes of liver diseases, and liver histology compatible with autoimmune hepatitis.

RESULTS

Four groups were identified: (1) 12 with increased serum gamma globulin concentrations; (2) 10 with normal or low serum gamma globulins and no combined blood disease; (3) 10 with combined aplastic anemia; and (4) 6 with peripheral thrombocytopenia with/without neutropenia. Immunosuppressive treatment was associated with aminotransferases normalization in all but one child who required liver transplantation. Relapses occurred in 10 children. Lymphocytopenia was found at the time of the diagnosis of hepatitis in 13 children, 12 in groups 3 or 4. All 38 children are alive after 4-17 years, 18 still under immunosuppression.

CONCLUSIONS

Childhood seronegative autoimmune hepatitis includes a spectrum of disorders. Early liver histology is recommended and, if compatible with autoimmune hepatitis, immunosuppressive treatment should be started. Initial lymphocytopenia may indicate future hematological complication.

摘要

背景

一些患有急性或慢性肝病的儿童表现出与自身免疫性肝炎相符的组织学特征,但缺乏特异性血清学标志物。

目的

描述儿童血清阴性自身免疫性肝炎的特征、治疗及预后。

方法

1988年至2010年,纳入38名儿童,符合以下标准:病毒学研究阴性、无血清自身抗体、排除其他肝病病因且肝脏组织学与自身免疫性肝炎相符。

结果

分为四组:(1)12名血清γ球蛋白浓度升高;(2)10名血清γ球蛋白正常或降低且无合并血液系统疾病;(3)10名合并再生障碍性贫血;(4)6名伴有外周血小板减少伴或不伴中性粒细胞减少。除1名需要肝移植的儿童外,免疫抑制治疗均使转氨酶恢复正常。10名儿童复发。13名儿童在肝炎诊断时发现淋巴细胞减少,其中12名在第3组或第4组。38名儿童在4至17年后均存活,18名仍在接受免疫抑制治疗。

结论

儿童血清阴性自身免疫性肝炎包括一系列疾病。建议早期进行肝脏组织学检查,若与自身免疫性肝炎相符,应开始免疫抑制治疗。初始淋巴细胞减少可能预示未来的血液学并发症。

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