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...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2022-01-01
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| Series: | MAMC Journal of Medical Sciences |
| Subjects: | |
| Online Access: | http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar |
| _version_ | 1798037370527809536 |
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| author | Shishir Kumar Shasanka Shekhar Panda Sujoy Neogi Simmi K Ratan |
| author_facet | Shishir Kumar Shasanka Shekhar Panda Sujoy Neogi Simmi K Ratan |
| author_sort | Shishir Kumar |
| collection | DOAJ |
| description | 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. |
| first_indexed | 2024-04-11T21:25:39Z |
| format | Article |
| id | doaj.art-38cb46d59a724e7f9609a22d7720407d |
| institution | Directory Open Access Journal |
| issn | 2394-7438 |
| language | English |
| last_indexed | 2024-04-11T21:25:39Z |
| publishDate | 2022-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | MAMC Journal of Medical Sciences |
| spelling | doaj.art-38cb46d59a724e7f9609a22d7720407d2022-12-22T04:02:24ZengWolters Kluwer Medknow PublicationsMAMC Journal of Medical Sciences2394-74382022-01-018217817910.4103/mamcjms.mamcjms_79_21Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare PresentationShishir KumarShasanka Shekhar PandaSujoy NeogiSimmi K RatanAbstract 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.http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumarcongenital cystic adenomatoid malformationempyemaspontaneous resolution |
| spellingShingle | Shishir Kumar Shasanka Shekhar Panda Sujoy Neogi Simmi K Ratan Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation MAMC Journal of Medical Sciences congenital cystic adenomatoid malformation empyema spontaneous resolution |
| title | Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
| title_full | Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
| title_fullStr | Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
| title_full_unstemmed | Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
| title_short | Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation |
| title_sort | spontaneous resolution of type 1 macrocystic congenital cystic adenomatoid malformation a rare presentation |
| topic | congenital cystic adenomatoid malformation empyema spontaneous resolution |
| url | http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar |
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