Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/82050
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Type: Journal article
Title: Congenital cystic adenomatoid malformation with associated mucinous bronchioloalveolar carcinoma in a neonate
Author: Li, J.
Chen, G.
Zhang, X.
Moore, L.
Cheng, H.
Citation: Fetal and Pediatric Pathology, 2014; 33(1):29-34
Publisher: Informa Healthcare
Issue Date: 2014
ISSN: 1551-3815
1551-3823
Statement of
Responsibility: 
Juan Li, Guang-Sheng Chen, Xiaohui Zhang, Lynette Moore and Hong Cheng
Abstract: Congenital cystic adenomatoid malformation (CCAM) of lung is a rare hamartomatous disorder characterized by abnormal branching morphogenesis of the lung. We report an unusual case of a 2-day-old male newborn with a pulmonary cystic lesion and lobectomy revealed a CCAM of the lung that has overlapping features of type 1 and type 2, complicating with multifocal mucinous bronchioloalveolar carcinoma (BAC). The case indicates that malignant transformation can occur in very early stage of the infancy in the patients with CCAM of lung.
Keywords: lung; congenital cystic adenomatoid malformation; bronchioloalveolar carcinoma; congenital pulmonary airway malformation
Rights: Copyright © Informa Healthcare USA, Inc.
RMID: 0020134140
DOI: 10.3109/15513815.2013.842272
Appears in Collections:Paediatrics publications

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