MeSH Browser

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

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Cystic Adenomatoid Malformation of Lung, Congenital MeSH Descriptor Data 2023