Pulmonary cystic adenomatoid malformation in an adult patient: An underdiagnosed disease

被引：3

作者：

Metivier, A. -C. ^{[1
]}

Denoux, Y. ^{[2
]}

Tcherakian, C. ^{[1
,3
,4
]}

Puyo, P. ^{[5
]}

Rivaud, E. ^{[1
]}

Mellot, F. ^{[6
]}

Honderlick, P. ^{[7
]}

Couderc, L. -J. ^{[1
,3
,4
]}

机构：

[1] Hop Foch, Serv Pneumol, F-92151 Suresnes, France

[2] Hop Foch, Serv Anat Pathol, F-92150 Suresnes, France

[3] Univ Versailles St Quentin En Yvelines, Fac Med, Guyancourt, France

[4] Univ Versailles St Quentin En Yvelines, UPRES, F-78280 Guyancourt, France

[5] Hop Foch, Serv Chirurg Thorac, F-92150 Suresnes, France

[6] Hop Foch, Serv Radiol, F-92150 Suresnes, France

[7] Hop Foch, Microbiol Lab, F-92150 Suresnes, France

来源：

REVUE DE PNEUMOLOGIE CLINIQUE | 2011年 / 67卷 / 04期

关键词：

Cystic adenomatoid malformation; Tuberculosis; LUNG; CLASSIFICATION;

D O I：

10.1016/j.pneumo.2011.04.001

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

Currently, most congenital tower respiratory tract malformations are detected during pregnancy or at birth, thanks to antenatal imaging. However, a pulmonary congenital cystic adenomatoid disease may be found in adulthood. The diagnosis is difficult, due to its rarity. We present the case of a patient whose diagnosis of pulmonary cystic adenomatoid malformation was confirmed when she had tuberculosis. A lobectomy was performed, which enabled identification of tuberculosis and also multiple cysts of adenomatoid malformation. The risk posed by this malformation, i.e. the risk of developing bronchioloalveolar carcinoma and of infection or pneumothorax, is the incentive for proposing formal surgical removal. (C) 2011 Published by Elsevier Masson SAS.

引用

页码：275 / 280

页数：6

共 20 条

[1] Medical progress - Bronchiectasis [J].