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儿童先天性肺气道畸形中发生的细支气管肺泡癌:病例报告及该关联的最新情况

Bronchioloalveolar carcinoma arising in a congenital pulmonary airway malformation in a child: case report with an update of this association.

作者信息

Ramos Simone G, Barbosa Gustavo H, Tavora Fabio R, Jeudy Jean, Torres Lidia A G M, Tone Luiz Gonzaga, Trad Clovis S

机构信息

Department of Pathology, Faculty of Medicine of Ribeirão Preto, University of São Paulo, 14049-900 Ribeirão Preto, São Paulo, Brazil.

出版信息

J Pediatr Surg. 2007 May;42(5):E1-4. doi: 10.1016/j.jpedsurg.2007.02.003.

Abstract

An 8-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.

摘要

一名8岁女孩因左肺叶肿块接受评估。她的临床病史显示,自2岁起就有间歇性干咳,伴有反复咳脓痰和发热。她接受了左下肺叶切除术,病理检查发现是起源于1型先天性肺气道畸形的细支气管肺泡癌。未采取其他治疗措施。切除术后两年,影像学检查显示对侧有5个肺结节,提示疾病播散,预后不良。本文对该病例的临床表现、治疗及预后进行了回顾。

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