Congenital cystic adenomatoid malformation with associated mucinous bronchioloalveolar carcinoma in a neonate

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dc.contributor.authorLi, J.
dc.contributor.authorChen, G.
dc.contributor.authorZhang, X.
dc.contributor.authorMoore, L.
dc.contributor.authorCheng, H.
dc.date.issued2014
dc.description.abstractCongenital 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.
dc.description.statementofresponsibilityJuan Li, Guang-Sheng Chen, Xiaohui Zhang, Lynette Moore and Hong Cheng
dc.identifier.citationFetal and Pediatric Pathology, 2014; 33(1):29-34
dc.identifier.doi10.3109/15513815.2013.842272
dc.identifier.issn1551-3815
dc.identifier.issn1551-3823
dc.identifier.urihttp://hdl.handle.net/2440/82050
dc.language.isoen
dc.publisherInforma Healthcare
dc.rightsCopyright © Informa Healthcare USA, Inc.
dc.source.urihttps://doi.org/10.3109/15513815.2013.842272
dc.subjectlung
dc.subjectcongenital cystic adenomatoid malformation
dc.subjectbronchioloalveolar carcinoma
dc.subjectcongenital pulmonary airway malformation
dc.titleCongenital cystic adenomatoid malformation with associated mucinous bronchioloalveolar carcinoma in a neonate
dc.typeJournal article
pubs.publication-statusPublished

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