Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/82050
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DC Field | Value | Language |
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dc.contributor.author | Li, J. | - |
dc.contributor.author | Chen, G. | - |
dc.contributor.author | Zhang, X. | - |
dc.contributor.author | Moore, L. | - |
dc.contributor.author | Cheng, H. | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Fetal and Pediatric Pathology, 2014; 33(1):29-34 | - |
dc.identifier.issn | 1551-3815 | - |
dc.identifier.issn | 1551-3823 | - |
dc.identifier.uri | http://hdl.handle.net/2440/82050 | - |
dc.description.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. | - |
dc.description.statementofresponsibility | Juan Li, Guang-Sheng Chen, Xiaohui Zhang, Lynette Moore and Hong Cheng | - |
dc.language.iso | en | - |
dc.publisher | Informa Healthcare | - |
dc.rights | Copyright © Informa Healthcare USA, Inc. | - |
dc.source.uri | http://dx.doi.org/10.3109/15513815.2013.842272 | - |
dc.subject | lung | - |
dc.subject | congenital cystic adenomatoid malformation | - |
dc.subject | bronchioloalveolar carcinoma | - |
dc.subject | congenital pulmonary airway malformation | - |
dc.title | Congenital cystic adenomatoid malformation with associated mucinous bronchioloalveolar carcinoma in a neonate | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.3109/15513815.2013.842272 | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest 4 Paediatrics publications |
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