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...

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Bibliographic Details
Main Authors: Shishir Kumar, Shasanka Shekhar Panda, Sujoy Neogi, Simmi K Ratan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
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
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Summary: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.
ISSN:2394-7438