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,...
Ausführliche Beschreibung
Autor*in: |
Deepak Talwar [verfasserIn] Onkar Jha [verfasserIn] Rahul Kumar Sharma [verfasserIn] Rajat Saxena [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: Lung India - Wolters Kluwer Medknow Publications, 2009, 34(2017), 1, Seite 88-91 |
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Übergeordnetes Werk: |
volume:34 ; year:2017 ; number:1 ; pages:88-91 |
Links: |
Link aufrufen |
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DOI / URN: |
10.4103/0970-2113.197121 |
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Katalog-ID: |
DOAJ002146797 |
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10.4103/0970-2113.197121 doi (DE-627)DOAJ002146797 (DE-599)DOAJc6db7b861e9d4921a3f52a5295140291 DE-627 ger DE-627 rakwb eng RC705-779 Deepak Talwar verfasserin aut Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier 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. Congenital cystic adenomatoid malformation congenital lung disease pulmonary cyst Diseases of the respiratory system Onkar Jha verfasserin aut Rahul Kumar Sharma verfasserin aut Rajat Saxena verfasserin aut In Lung India Wolters Kluwer Medknow Publications, 2009 34(2017), 1, Seite 88-91 (DE-627)558697895 (DE-600)2410801-7 0974598X nnns volume:34 year:2017 number:1 pages:88-91 https://doi.org/10.4103/0970-2113.197121 kostenfrei https://doaj.org/article/c6db7b861e9d4921a3f52a5295140291 kostenfrei http://www.lungindia.com/article.asp?issn=0970-2113;year=2017;volume=34;issue=1;spage=88;epage=91;aulast=Talwar kostenfrei https://doaj.org/toc/0970-2113 Journal toc kostenfrei https://doaj.org/toc/0974-598X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 34 2017 1 88-91 |
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Perpetual dilemma: Pleural or parenchymal/congenital or acquired solitary cystic lesion with fluid level |
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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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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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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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