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一例罕见的可变免疫缺陷病例,伴有II型免疫球蛋白异常血症、轻链缺陷、肠道相关IgA缺乏和进行性中性粒细胞减少。

A rare case of variable immune deficiency with type II dysgammaglobulinaemia, light chain defect, gut associated IgA deficiency and progressive neutropenia.

作者信息

Saha K, Chopra K, Dutta B R

出版信息

Asian Pac J Allergy Immunol. 1985 Dec;3(2):205-11.

PMID:3935129
Abstract

This report describes in detail an unusual variant of a common variable immunodeficiency disease in a seven-year-old boy. The unique features were progressive neutropenia due to defective myelopoiesis, serum IgG and IgA deficiencies, defective immunoglobulin light-chain synthesis, absence of secretory IgA and IgM gammopathy. He had been born healthy, but following a thermal injury at the age of 1 1/2 years, he suffered recurrent attacks of sinopulmonary and urinary tract infections, enteritis due to enteropathogenic E. coli, Giardia lamblia and E. histolytica, developed pulmonary tuberculosis and died of deep mycotic infection of the oral cavity and obstruction of the bronchial tree. The cause of the defective myelopoiesis could not be determined, but it might have been due to prolonged sulphomamide therapy administered for controlling his persistent urinary tract infection due to paraphymosis.

摘要

本报告详细描述了一名7岁男孩常见可变免疫缺陷病的一种不寻常变体。其独特特征包括由于骨髓生成缺陷导致的进行性中性粒细胞减少、血清IgG和IgA缺乏、免疫球蛋白轻链合成缺陷、分泌型IgA缺乏和IgM丙种球蛋白病。他出生时健康,但在1岁半时遭受热损伤后,反复出现鼻窦肺部和尿路感染、致病性大肠杆菌、蓝氏贾第鞭毛虫和溶组织内阿米巴引起的肠炎,患上肺结核,并死于口腔深部霉菌感染和支气管树阻塞。骨髓生成缺陷的原因无法确定,但可能是由于为控制因包茎引起的持续性尿路感染而长期使用磺胺类药物治疗所致。

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