Diagnosis and intervention of congenital cystic adenomatoid malformation / 国际儿科学杂志
International Journal of Pediatrics
;
(6): 790-793, 2019.
Artigo
em Chinês
| WPRIM
| ID: wpr-823442
ABSTRACT
Congenital cystic adenomatoid malformation (CCAM) is a rare cystic lung disease with an incidence rate ranging from 1/35 000 to 1/25 000 births.The mechanism is still unclear and is regarded a non-hereditary anomaly caused by arrest of lung.In some countries,over 99% of CCAMs were diagnosed by fetal sonography at gestational age of 18 ~ 20 weeks.Chest X-ray and CT are common methods to detect the CCAMs after birth.Newborns with CCAM may present with respiratory distress,but most patients are asymptomatic in life.Although many methods for diagnosis and treatment were suggested,no unified guideline is provided yet.Herein,we reviewed the advances in the mechanism,diagnosis and treatment of CCAM to highlight this rare event.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo diagnóstico
/
Guia de Prática Clínica
Idioma:
Chinês
Revista:
International Journal of Pediatrics
Ano de publicação:
2019
Tipo de documento:
Artigo
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