Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level

Congenital cystic adenomatoid malformations (CCAMs) are rare congenital, nonhereditary developmental anomalies of the lung with unknown etiology. CCAM is predominantly a disorder of infancy with the majority of the cases being diagnosed within the first 2 years of life. When CCAM presents in adults,...

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Main Authors: Deepak Talwar, Onkar Jha, Rahul Kumar Sharma, Rajat Saxena
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Lung India
Subjects:
Online Access:http://www.lungindia.com/article.asp?issn=0970-2113;year=2017;volume=34;issue=1;spage=88;epage=91;aulast=Talwar
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author Deepak Talwar
Onkar Jha
Rahul Kumar Sharma
Rajat Saxena
author_facet Deepak Talwar
Onkar Jha
Rahul Kumar Sharma
Rajat Saxena
author_sort Deepak Talwar
collection DOAJ
description Congenital cystic adenomatoid malformations (CCAMs) are rare congenital, nonhereditary developmental anomalies of the lung with unknown etiology. CCAM is predominantly a disorder of infancy with the majority of the cases being diagnosed within the first 2 years of life. When CCAM presents in adults, it represents a diagnostic dilemma and requires careful evaluation. We here report a case of large solitary congenital pulmonary cystic adenomatoid malformation with infection and hemorrhage, which was diagnosed as encysted hydropneumothorax on computerized tomography scans but turned out to be infected pulmonary cystic adenomatoid malformation after surgical excision.
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spelling doaj.art-c6db7b861e9d4921a3f52a52951402912022-12-21T18:51:12ZengWolters Kluwer Medknow PublicationsLung India0970-21130974-598X2017-01-01341889110.4103/0970-2113.197121Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid levelDeepak TalwarOnkar JhaRahul Kumar SharmaRajat SaxenaCongenital cystic adenomatoid malformations (CCAMs) are rare congenital, nonhereditary developmental anomalies of the lung with unknown etiology. CCAM is predominantly a disorder of infancy with the majority of the cases being diagnosed within the first 2 years of life. When CCAM presents in adults, it represents a diagnostic dilemma and requires careful evaluation. We here report a case of large solitary congenital pulmonary cystic adenomatoid malformation with infection and hemorrhage, which was diagnosed as encysted hydropneumothorax on computerized tomography scans but turned out to be infected pulmonary cystic adenomatoid malformation after surgical excision.http://www.lungindia.com/article.asp?issn=0970-2113;year=2017;volume=34;issue=1;spage=88;epage=91;aulast=TalwarCongenital cystic adenomatoid malformationcongenital lung diseasepulmonary cyst
spellingShingle Deepak Talwar
Onkar Jha
Rahul Kumar Sharma
Rajat Saxena
Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
Lung India
Congenital cystic adenomatoid malformation
congenital lung disease
pulmonary cyst
title Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
title_full Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
title_fullStr Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
title_full_unstemmed Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
title_short Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level
title_sort perpetual dilemma pleural or parenchymal congenital or acquired solitary cystic lesion with fluid level
topic Congenital cystic adenomatoid malformation
congenital lung disease
pulmonary cyst
url http://www.lungindia.com/article.asp?issn=0970-2113;year=2017;volume=34;issue=1;spage=88;epage=91;aulast=Talwar
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AT rahulkumarsharma perpetualdilemmapleuralorparenchymalcongenitaloracquiredsolitarycysticlesionwithfluidlevel
AT rajatsaxena perpetualdilemmapleuralorparenchymalcongenitaloracquiredsolitarycysticlesionwithfluidlevel