Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the sponta...
Ausführliche Beschreibung
Autor*in: |
Shishir Kumar [verfasserIn] Shasanka Shekhar Panda [verfasserIn] Sujoy Neogi [verfasserIn] Simmi K Ratan [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2022 |
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Übergeordnetes Werk: |
In: MAMC Journal of Medical Sciences - Wolters Kluwer Medknow Publications, 2019, 8(2022), 2, Seite 178-179 |
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Übergeordnetes Werk: |
volume:8 ; year:2022 ; number:2 ; pages:178-179 |
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DOI / URN: |
10.4103/mamcjms.mamcjms_79_21 |
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Katalog-ID: |
DOAJ078929946 |
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10.4103/mamcjms.mamcjms_79_21 doi (DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d DE-627 ger DE-627 rakwb eng Shishir Kumar verfasserin aut Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. congenital cystic adenomatoid malformation empyema spontaneous resolution Medicine R Shasanka Shekhar Panda verfasserin aut Sujoy Neogi verfasserin aut Simmi K Ratan verfasserin aut In MAMC Journal of Medical Sciences Wolters Kluwer Medknow Publications, 2019 8(2022), 2, Seite 178-179 (DE-627)174282823X 23950145 nnns volume:8 year:2022 number:2 pages:178-179 https://doi.org/10.4103/mamcjms.mamcjms_79_21 kostenfrei https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d kostenfrei http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar kostenfrei https://doaj.org/toc/2394-7438 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA 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_2014 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 8 2022 2 178-179 |
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10.4103/mamcjms.mamcjms_79_21 doi (DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d DE-627 ger DE-627 rakwb eng Shishir Kumar verfasserin aut Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. congenital cystic adenomatoid malformation empyema spontaneous resolution Medicine R Shasanka Shekhar Panda verfasserin aut Sujoy Neogi verfasserin aut Simmi K Ratan verfasserin aut In MAMC Journal of Medical Sciences Wolters Kluwer Medknow Publications, 2019 8(2022), 2, Seite 178-179 (DE-627)174282823X 23950145 nnns volume:8 year:2022 number:2 pages:178-179 https://doi.org/10.4103/mamcjms.mamcjms_79_21 kostenfrei https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d kostenfrei http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar kostenfrei https://doaj.org/toc/2394-7438 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA 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_2014 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 8 2022 2 178-179 |
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10.4103/mamcjms.mamcjms_79_21 doi (DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d DE-627 ger DE-627 rakwb eng Shishir Kumar verfasserin aut Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. congenital cystic adenomatoid malformation empyema spontaneous resolution Medicine R Shasanka Shekhar Panda verfasserin aut Sujoy Neogi verfasserin aut Simmi K Ratan verfasserin aut In MAMC Journal of Medical Sciences Wolters Kluwer Medknow Publications, 2019 8(2022), 2, Seite 178-179 (DE-627)174282823X 23950145 nnns volume:8 year:2022 number:2 pages:178-179 https://doi.org/10.4103/mamcjms.mamcjms_79_21 kostenfrei https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d kostenfrei http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar kostenfrei https://doaj.org/toc/2394-7438 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA 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_2014 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 8 2022 2 178-179 |
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10.4103/mamcjms.mamcjms_79_21 doi (DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d DE-627 ger DE-627 rakwb eng Shishir Kumar verfasserin aut Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. congenital cystic adenomatoid malformation empyema spontaneous resolution Medicine R Shasanka Shekhar Panda verfasserin aut Sujoy Neogi verfasserin aut Simmi K Ratan verfasserin aut In MAMC Journal of Medical Sciences Wolters Kluwer Medknow Publications, 2019 8(2022), 2, Seite 178-179 (DE-627)174282823X 23950145 nnns volume:8 year:2022 number:2 pages:178-179 https://doi.org/10.4103/mamcjms.mamcjms_79_21 kostenfrei https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d kostenfrei http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar kostenfrei https://doaj.org/toc/2394-7438 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA 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_2014 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 8 2022 2 178-179 |
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10.4103/mamcjms.mamcjms_79_21 doi (DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d DE-627 ger DE-627 rakwb eng Shishir Kumar verfasserin aut Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. congenital cystic adenomatoid malformation empyema spontaneous resolution Medicine R Shasanka Shekhar Panda verfasserin aut Sujoy Neogi verfasserin aut Simmi K Ratan verfasserin aut In MAMC Journal of Medical Sciences Wolters Kluwer Medknow Publications, 2019 8(2022), 2, Seite 178-179 (DE-627)174282823X 23950145 nnns volume:8 year:2022 number:2 pages:178-179 https://doi.org/10.4103/mamcjms.mamcjms_79_21 kostenfrei https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d kostenfrei http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar kostenfrei https://doaj.org/toc/2394-7438 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA 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_2014 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 8 2022 2 178-179 |
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Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation congenital cystic adenomatoid malformation empyema spontaneous resolution |
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Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
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Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. |
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Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. |
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Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare. |
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