PiSZ-phenotype alpha 1-antitrypsin deficiency: a rare cause of bronchiectasis

被引:0
|
作者
Veloso, S
Aguilar, X
Paniagua, MJ
Vidal, F
Richart, C
机构
[1] Univ Rovira & Virgili, Unidad Neumol La Planta, Inst Destudis Avancats, Hosp Univ Juan XXIII, Tarragona 43007, Spain
[2] Univ Rovira & Virgili, Med Interna Serv, Inst Destudis Avancats, Hosp Univ Juan XXIII, Tarragona 43007, Spain
来源
ARCHIVOS DE BRONCONEUMOLOGIA | 2002年 / 38卷 / 05期
关键词
alpha; 1-antitrypsin; PiSZ phenotype; bronchiectasis;
D O I
10.1016/S0300-2896(02)75204-6
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Panacinar emphysema is the most characteristic pulmonary disease in patients with alpha 1-antitrypsin deficiency (AAT). Bronchiectasis can also arise with AAT deficiency, although the association is much less common and no clear cause-effect relationship has yet been established. We report the case of a woman who presented with bronchiectasis and PiSZ-phenotype ATT deficiency, without emphysema. A review of the literature showed that the case is exceptional.
引用
收藏
页码:249 / 250
页数:2
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