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Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature

Congenital cystic adenomatoid malformation (CCAM), also named congenital pulmonary airway malformation (CPAM), is a congenital abnormality of lung which is uncommon in adults. Here we present 2 adult cases of CCAM with unusual clinical and pathologic findings. One case was complicated with aspergill...

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Autores principales: Feng, Anning, Cai, Hourong, Sun, Qi, Zhang, Yifen, Chen, Lulu, Meng, Fanqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349468/
https://www.ncbi.nlm.nih.gov/pubmed/22472365
http://dx.doi.org/10.1186/1746-1596-7-37
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author Feng, Anning
Cai, Hourong
Sun, Qi
Zhang, Yifen
Chen, Lulu
Meng, Fanqing
author_facet Feng, Anning
Cai, Hourong
Sun, Qi
Zhang, Yifen
Chen, Lulu
Meng, Fanqing
author_sort Feng, Anning
collection PubMed
description Congenital cystic adenomatoid malformation (CCAM), also named congenital pulmonary airway malformation (CPAM), is a congenital abnormality of lung which is uncommon in adults. Here we present 2 adult cases of CCAM with unusual clinical and pathologic findings. One case was complicated with aspergillosis which was seldom reported. The other case was suffered bilateral lesions and the patient's mother had been previously radiographically discovered bilateral cystic lesions that CCAM could not be ruled out. A review of currently published related literatures has also been provided. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/6406766736634578.
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spelling pubmed-33494682012-05-11 Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature Feng, Anning Cai, Hourong Sun, Qi Zhang, Yifen Chen, Lulu Meng, Fanqing Diagn Pathol Case Report Congenital cystic adenomatoid malformation (CCAM), also named congenital pulmonary airway malformation (CPAM), is a congenital abnormality of lung which is uncommon in adults. Here we present 2 adult cases of CCAM with unusual clinical and pathologic findings. One case was complicated with aspergillosis which was seldom reported. The other case was suffered bilateral lesions and the patient's mother had been previously radiographically discovered bilateral cystic lesions that CCAM could not be ruled out. A review of currently published related literatures has also been provided. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/6406766736634578. BioMed Central 2012-04-03 /pmc/articles/PMC3349468/ /pubmed/22472365 http://dx.doi.org/10.1186/1746-1596-7-37 Text en Copyright ©2012 Feng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Feng, Anning
Cai, Hourong
Sun, Qi
Zhang, Yifen
Chen, Lulu
Meng, Fanqing
Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title_full Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title_fullStr Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title_full_unstemmed Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title_short Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
title_sort congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349468/
https://www.ncbi.nlm.nih.gov/pubmed/22472365
http://dx.doi.org/10.1186/1746-1596-7-37
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