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Cystic Adenomatoid Malformation of Lung, Congenital MeSH Descriptor Data 2024


MeSH Heading
Cystic Adenomatoid Malformation of Lung, Congenital
Tree Number(s)
C08.381.150
C08.695.290
C16.131.740.290
Unique ID
D015615
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D015615
Annotation
do not use / congen & do not coordinate with INFANT, NEWBORN, DISEASES
Scope Note
An abnormality in lung development that is characterized by a multicystic mass resulting from an adenomatous overgrowth of the terminal BRONCHIOLES with a consequent reduction of PULMONARY ALVEOLI. This anomaly is classified into three types by the cyst size.
Entry Version
CCAM
Entry Term(s)
Congenital Cystic Adenomatoid Malformation
Congenital Cystic Adenomatoid Malformation of Lung
Congenital Cystic Adenomatoid Malformation, Type 1
Congenital Cystic Adenomatoid Malformation, Type 2
Congenital Cystic Adenomatoid Malformation, Type 3
Congenital Cystic Adenomatoid Malformation, Type I
Congenital Cystic Adenomatoid Malformation, Type II
Congenital Cystic Adenomatoid Malformation, Type III
Cystic Adenomatoid Malformation of Lung
Lung Malformation, Congenital Cystic Adenomatoid
Lung Malformation, Cystic Adenomatoid, Congenital
Previous Indexing
Lung/abnormalities (1966-1989)
Public MeSH Note
90
History Note
90
Date Established
1990/01/01
Date of Entry
1989/04/07
Revision Date
2013/07/09
Cystic Adenomatoid Malformation of Lung, Congenital Preferred
Congenital Cystic Adenomatoid Malformation, Type I Narrower
Congenital Cystic Adenomatoid Malformation, Type II Narrower
Congenital Cystic Adenomatoid Malformation, Type III Narrower
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