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Bronchioloalveolar carcinoma arising in a congenital pulmonary airway malformation in a child: case report with an update of this association
被引:56
|作者:
Ramos, Simone G.
[1
]
Barbosa, Gustavo H.
Tavora, Fabio R.
Jeudy, Jean
Torres, Lidia A. G. M.
Tone, Luiz Gonzaga
Trad, Clovis S.
机构:
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Pathol, BR-14049900 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Pediat, BR-14049900 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Radiol, BR-14049900 Ribeirao Preto, Brazil
[4] Univ Maryland, Dept Pathol, College Pk, MD 20742 USA
[5] Univ Maryland, Dept Radiol, College Pk, MD 20742 USA
关键词:
bronchioloalveolar carcinoma;
congenital pulmonary airway malformation;
child;
lung cancer;
adenocarcinoma;
mucinous metaplasia;
D O I:
10.1016/j.jpedsurg.2007.02.003
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
An 9-year-old girl was evaluated for a mass in the left pulmonary lobe. Her clinical history was remarkable for an intermittent dry cough since the age of 2, with recurrent episodes of purulent sputum and fever. She underwent left lower lobectomy, which was found to be a bronchioloalveolar carcinoma arising in a type 1 congenital pulmonary airway malformation at pathologic examination. No additional therapies were undertaken. Two years after resection, imaging studies showed 5 contralateral pulmonary nodules suggestive of disseminated disease with a poor outcome. A review of presentation, treatment, and outcome of this association was made. (C) 2007 Elsevier Inc. All rights reserved.
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页码:e1 / e4
页数:7
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