Severe Axillary Lymphadenitis After BCG Vaccination: Alert for Primary Immunodeficiencies

被引:37
作者
Santos, Alexandra [1 ,2 ]
Dias, Andrea [1 ]
Cordeiro, Ana [1 ]
Cordinha, Carolina [1 ]
Lemos, Sonia [2 ]
Rocha, Graca [3 ]
Faria, Emilia [2 ]
机构
[1] Coimbra Pediat Hosp, Med Inpatient Dept, Coimbra, Portugal
[2] Coimbra Pediat Hosp, Primary Immunodeficiencies Outpatient Clin, Coimbra, Portugal
[3] Coimbra Pediat Hosp, Infect Dis Outpatient Clin, Coimbra, Portugal
关键词
BCG; immunodeficiency; interferon-gamma receptor 1 deficiency; tuberculosis; ZAP70; deficiency; CALMETTE-GUERIN INFECTION; TUBERCULOSIS; DEFICIENCY; DISORDERS; IMMUNITY; DISEASE; CHILD;
D O I
10.1016/S1684-1182(10)60082-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The bacilli Calmette-Guerin (BCG) vaccine is administered to all newborns in countries where tuberculosis is endemic. Immunocompromised hosts, namely patients with human immunodeficiency virus infection or primary immunodeficiencies, are especially prone to serious complications from this vaccine. We report three cases of BCG disease in children with primary immunodeficiencies: one with a partial recessive interferon-gamma receptor 1 deficiency, who developed BCG dissemination; and two relatives with ZAP70 deficiency, a severe combined immunodeficiency, both of whom presented with regional and distant BCG disease. All had severe axillary lymphadenitis. These clinical cases underline the importance of considering the diagnosis of immunodeficiency in a child with severe axillary lymphadenitis after BCG vaccination and of disseminated BCG disease in an immunodeficient child in the appropriate clinical setting. Moreover, BCG vaccination should be delayed in every newborn with a family history of primary immunodeficiency until the condition has been ruled out.
引用
收藏
页码:530 / 537
页数:8
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