Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Should asymptomatic congenital cystic adenomatous malformations be removed? The case against

Kotecha, Sailesh 2013. Should asymptomatic congenital cystic adenomatous malformations be removed? The case against. Paediatric Respiratory Reviews 14 (3) , pp. 171-172. 10.1016/j.prrv.2013.06.002

Full text not available from this repository.

Abstract

In this article, we debate the pros and cons for the surgical removal of asymptomatic antenatally diagnosed cystic adenomatous malformations (CCAM). It is often argued that asymptomatic antenatally diagnosed CCAMs should be surgically removed in infancy due to the risk of future malignancy, future risk of infection and other symptoms and of increased risk of surgery after infective episodes. However, the risk of malignancy is often overplayed and the risk may not even be decreased after excision of the CCAM. Furthermore, the risk of future symptoms is uncertain thus surgical removal will subject many infants to unnecessary risk. Medical follow up will decrease the numbers that undergo surgical intervention and newer imaging techniques are likely to decrease the radiation risk. Whichever route of management is followed there is an urgent need to outline the natural history of asymptomatic CCAMs.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Subjects: R Medicine > R Medicine (General)
R Medicine > RJ Pediatrics
Uncontrolled Keywords: Congenital thoracic malformation, Pulmonary sequestration, Congenital cystic adenomatous malformations
Additional Information: Available online 17 July 2013
Publisher: Elsevier
ISSN: 1526-0542
Last Modified: 04 Jun 2017 08:16
URI: http://orca-mwe.cf.ac.uk/id/eprint/75142

Citation Data

Cited 20 times in Google Scholar. View in Google Scholar

Cited 21 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item