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

页码：249 / 250

页数：2

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