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中国儿童原发性免疫缺陷病的发病特征和分布(2004-2009)。

Distribution and clinical features of primary immunodeficiency diseases in Chinese children (2004-2009).

机构信息

Department of Pediatrics, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.

出版信息

J Clin Immunol. 2011 Jun;31(3):297-308. doi: 10.1007/s10875-010-9493-3. Epub 2011 Jan 18.

DOI:10.1007/s10875-010-9493-3
PMID:21243521
Abstract

Two hundred and one patients have been diagnosed with primary immunodeficiency diseases (PIDs) in our center from January 2004 to December 2009. The male-to-female ratio was 5.29:1. Spectrums of PIDs were as follows: predominantly antibody deficiency disease was the most common category (94 patients, 48.2%), followed by other well-defined immunodeficiency syndromes (40 patients, 20.5%), combined T and B cell immunodeficiencies (33 patients, 16.9%), congenital defects of phagocyte number and/or function (21 patients, 10.8%), and diseases of immune dysregulation (six patients, 3.1%). Agammaglobulinemia was the most frequent disease type. The median of diagnosis lag was 18.0 months. Pneumonia was the most common manifestation of PID patients. Some manifestations were prone to concentrate in certain diseases. As for therapy, 99 patients (50.8%) received intravenous immunoglobulin replacement therapy; 13 patients received hematopoietic stem cell transplantation and nine of them were still alive. In this study, we sought to describe and analyze the distribution, clinical features, and therapy methods of PIDs among children diagnosed in our country and to compare with reports from other countries and regions.

摘要

从 2004 年 1 月至 2009 年 12 月,我们中心共诊断出 201 例原发性免疫缺陷病(PID)患者。男女比例为 5.29:1。PID 谱如下:以抗体缺陷病为主,最常见(94 例,占 48.2%),其次为其他明确的免疫缺陷综合征(40 例,占 20.5%)、T 和 B 细胞联合免疫缺陷(33 例,占 16.9%)、吞噬细胞数量和/或功能先天性缺陷(21 例,占 10.8%)和免疫调节紊乱性疾病(6 例,占 3.1%)。丙种球蛋白缺乏症是最常见的疾病类型。中位诊断延迟时间为 18.0 个月。肺炎是 PID 患者最常见的表现。某些表现易集中在某些疾病中。在治疗方面,99 例(50.8%)患者接受静脉注射免疫球蛋白替代治疗;13 例患者接受造血干细胞移植,其中 9 例仍存活。在这项研究中,我们试图描述和分析我国诊断出的儿童 PID 的分布、临床特征和治疗方法,并与其他国家和地区的报告进行比较。

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2
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J Gastroenterol Hepatol. 2010 Mar;25(3):453-68. doi: 10.1111/j.1440-1746.2010.06241.x.
3
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Immune Netw. 2022 Aug 4;22(4):e30. doi: 10.4110/in.2022.22.e30. eCollection 2022 Aug.
4
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Front Immunol. 2022 Apr 21;13:900091. doi: 10.3389/fimmu.2022.900091. eCollection 2022.
5
Current status and prospects of primary immunodeficiency diseases in Asia.亚洲原发性免疫缺陷病的现状与前景
Genes Dis. 2019 Sep 12;7(1):3-11. doi: 10.1016/j.gendis.2019.09.004. eCollection 2020 Mar.
6
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PLoS One. 2017 Apr 27;12(4):e0175867. doi: 10.1371/journal.pone.0175867. eCollection 2017.
7
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8
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J Clin Immunol. 2010 Jan;30(1):10-6. doi: 10.1007/s10875-009-9357-x. Epub 2010 Jan 26.
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