与IgG2缺乏相关的原发性高丙种球蛋白血症性紫癜。病例报告。
Primary hypergammaglobulinemic purpura associated with IgG2 deficiency. A case report.
作者信息
Venuta A, Penza R, Cellini M, Garetti E, Bergomi A, Pastorelli S, Massolo F
机构信息
Dipartimento di Scienze Ostetriche, Ginecologiche e Pediatriche, Università di Modena, Italy.
出版信息
Clin Exp Rheumatol. 1995 Sep-Oct;13(5):663-5.
PMID:8575150
Abstract
Hypergammaglobulinemic purpura is a rare disease in children. We report a case of a 12 year-old girl with a history of frequent infections. We found the presence of IgG2 deficiency despite polyclonal hypergammaglobulinemia. An IgG subclass determination should be obtained in every child with polyclonal hypergammaglobulinemia and features of immunodeficiency.
摘要
高丙种球蛋白血症性紫癜在儿童中是一种罕见疾病。我们报告一例12岁有频繁感染史的女孩病例。尽管有多克隆性高丙种球蛋白血症，我们仍发现存在IgG2缺乏。对于每一位有多克隆性高丙种球蛋白血症及免疫缺陷特征的儿童，均应进行IgG亚类测定。
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