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CASE REPORT
Year : 2022  |  Volume : 8  |  Issue : 2  |  Page : 178-179

Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation


Department of Pediatric Surgery, Maulana Azad Medical College (MAMC), New Delhi, India

Correspondence Address:
Shasanka Shekhar Panda
Associate Professor, Department of Paediatric Surgery, Maulana Azad Medical College (MAMC), New Delhi-110002
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/mamcjms.mamcjms_79_21

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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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