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|Title:||Congenital cystic adenomatoid malformation with associated mucinous bronchioloalveolar carcinoma in a neonate|
|Citation:||Fetal and Pediatric Pathology, 2014; 33(1):29-34|
|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.|
|Appears in Collections:||Paediatrics publications|
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