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Descriptor English: Cystic Adenomatoid Malformation of Lung, Congenital
Descriptor Spanish: Malformación Adenomatoide Quística Congénita del Pulmón
Descriptor malformación adenomatoide quística congénita del pulmón
Entry term(s) malformación adenomatoide quística congénita
Scope note: Anomalía del desarrollo pulmonar que se caracterizada por una masa multiquística que resulta de un sobrecrecimiento adenomatoso de los BRONQUIOLOS terminales, con la consiguiente reducción de ALVEOLOS PULMONARES. Esta anomalía se clasifica en tres tipos según el tamaño de los quistes.
Descriptor Portuguese: Malformação Adenomatoide Cística Congênita do Pulmão
Descriptor French: Malformation congénitale kystique adénomatoïde du poumon
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
Tree number(s): C08.381.150
C08.695.290
C16.131.740.290
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D015615
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.
Annotation: do not use / congen & do not coordinate with INFANT, NEWBORN, DISEASES
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Lung/abnormalities (1966-1989)
Public MeSH Note: 90
History Note: 90
Entry Version: CCAM
DeCS ID: 24597
Unique ID: D015615
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1990/01/01
Date of Entry: 1989/04/07
Revision Date: 2013/07/09
Cystic Adenomatoid Malformation of Lung, Congenital - Preferred
Concept UI M0023957
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.
Preferred term Cystic Adenomatoid Malformation of Lung, Congenital
Entry term(s) Congenital Cystic Adenomatoid Malformation
Congenital Cystic Adenomatoid Malformation of Lung
Cystic Adenomatoid Malformation of Lung
Lung Malformation, Congenital Cystic Adenomatoid
Lung Malformation, Cystic Adenomatoid, Congenital
Congenital Cystic Adenomatoid Malformation, Type III - Narrower
Concept UI M0518873
Scope note This type is characterized by a bulky solid mass with cysts of <0.5 cm.
Preferred term Congenital Cystic Adenomatoid Malformation, Type III
Entry term(s) Congenital Cystic Adenomatoid Malformation, Type 3
Congenital Cystic Adenomatoid Malformation, Type I - Narrower
Concept UI M0518871
Scope note This type is macrocystic, characterized by a single or multiple cysts of >2.5 cm.
Preferred term Congenital Cystic Adenomatoid Malformation, Type I
Entry term(s) Congenital Cystic Adenomatoid Malformation, Type 1
Congenital Cystic Adenomatoid Malformation, Type II - Narrower
Concept UI M0518872
Scope note This type is microcystic, characterized by multiple cysts of 0.5 to 2.5 cm.
Preferred term Congenital Cystic Adenomatoid Malformation, Type II
Entry term(s) Congenital Cystic Adenomatoid Malformation, Type 2



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