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特发性迟发性免疫球蛋白缺乏伴细胞介导免疫相关缺陷。

Idiopathic late-onset immunoglobulin deficiency with associated defect in cell-mediated immunity.

作者信息

Lo N S, Sin W K, Ho P C, Mak L W, Lawton J W

出版信息

Arch Dis Child. 1977 Nov;52(11):899-901. doi: 10.1136/adc.52.11.899.

Abstract

An 8-year-old boy presented with idiopathic late-onset immunoglobulin deficiency manifested principally by recurrent suppurative chest infections and chronic diarrhoea with malabsorption. Nodular lymphoid hyperplasia and giardiasis were shown on small bowel biopsy. Investigation of the immune system showed low serum levels of IgG, IgM, and IgA, negative skin tests to four recall antigens, absent mixed lymphocyte reactivity, and impared lymphocyte responses to mitogens in vitro. Serum complement and granulocyte function studies were normal. Maintenance therapy with gammaglobulin and antibiotics gave a good response.

摘要

一名8岁男孩表现为特发性迟发性免疫球蛋白缺乏,主要表现为反复化脓性胸部感染和伴有吸收不良的慢性腹泻。小肠活检显示有结节性淋巴组织增生和贾第虫病。免疫系统检查显示血清IgG、IgM和IgA水平低,对四种回忆抗原的皮肤试验阴性,混合淋巴细胞反应缺失,体外淋巴细胞对有丝分裂原的反应受损。血清补体和粒细胞功能研究正常。用丙种球蛋白和抗生素进行维持治疗反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f31e/1544829/e24a88457755/archdisch00811-0083-a.jpg

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