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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Autor*in:	Shishir Kumar [verfasserIn] Shasanka Shekhar Panda [verfasserIn] Sujoy Neogi [verfasserIn] Simmi K Ratan [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	congenital cystic adenomatoid malformation empyema spontaneous resolution

Übergeordnetes Werk:	In: MAMC Journal of Medical Sciences - Wolters Kluwer Medknow Publications, 2019, 8(2022), 2, Seite 178-179
Übergeordnetes Werk:	volume:8 ; year:2022 ; number:2 ; pages:178-179

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.4103/mamcjms.mamcjms_79_21

Katalog-ID:	DOAJ078929946

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author	Shishir Kumar
spellingShingle	Shishir Kumar misc congenital cystic adenomatoid malformation misc empyema misc spontaneous resolution misc Medicine misc R Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
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topic_title	Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation congenital cystic adenomatoid malformation empyema spontaneous resolution
topic	misc congenital cystic adenomatoid malformation misc empyema misc spontaneous resolution misc Medicine misc R
topic_unstemmed	misc congenital cystic adenomatoid malformation misc empyema misc spontaneous resolution misc Medicine misc R
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title	Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
ctrlnum	(DE-627)DOAJ078929946 (DE-599)DOAJ38cb46d59a724e7f9609a22d7720407d
title_full	Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
author_sort	Shishir Kumar
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author_browse	Shishir Kumar Shasanka Shekhar Panda Sujoy Neogi Simmi K Ratan
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title_sort	spontaneous resolution of type 1 macrocystic congenital cystic adenomatoid malformation: a rare presentation
title_auth	Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
abstract	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.
abstractGer	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.
abstract_unstemmed	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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title_short	Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation
url	https://doi.org/10.4103/mamcjms.mamcjms_79_21 https://doaj.org/article/38cb46d59a724e7f9609a22d7720407d http://www.mamcjms.in/article.asp?issn=2394-7438;year=2022;volume=8;issue=2;spage=178;epage=179;aulast=Kumar https://doaj.org/toc/2394-7438
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up_date	2024-07-03T20:40:53.770Z
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