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Автор CHUANG, SANDRA
Автор SUGO, ELLA
Автор JAFFE, ADAM
dc.description Congenital cystic adenomatoid malformations of the lung (CCAMs) were originally described by Ch'In and Tang in 1949 as rare lung lesions occurring in premature or stillborn infants with anasarca. In 1977 Stocker et al divided CCAM into three types based on their clinical and pathological features. The nomenclature has since changed to congenital pulmonary airway malformations (CPAMs) to reflect the possible absence of cystic changes and the probable underlying pathogenesis of different types. CPAMs are relatively rare congenital abnormalities with a reported incidence varying from 1 in 10,000 to 1 in 35,000. There is a slight male predominance, but no racial predilection has been noted. This review will outline the current nomenclature and features of different types of CPAMs, highlight possible mechanisms underlying the development of CPAMs, review current antenatal imaging modalities and interventions, address the debate surrounding the postnatal management of CPAMs, and suggest areas for future research.
Формат application.pdf
Издатель Cambridge University Press
Копирайт Copyright © Cambridge University Press 2009
Название A REVIEW OF POSTNATAL MANAGEMENT OF CONGENITAL PULMONARY AIRWAY MALFORMATIONS
Тип research-article
DOI 10.1017/S0965539509990052
Electronic ISSN 1469-5065
Print ISSN 0965-5395
Журнал Fetal and Maternal Medicine Review
Том 20
Первая страница 179
Последняя страница 204
Аффилиация CHUANG SANDRA; Department of Respiratory Medicine, Sydney Children's Hospital, Randwick, Sydney, Australia.
Аффилиация SUGO ELLA; Department of Anatomical Pathology, Prince of Wales Hospital, Randwick, Sydney, Australia.
Аффилиация JAFFE ADAM; University of New South Wales
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