Pesquisa
Descritor em português: Malformação Adenomatoide Cística Congênita do Pulmão
Descritor em inglês: Cystic Adenomatoid Malformation of Lung, Congenital
Descritor em espanhol: Malformación Adenomatoide Quística Congénita del Pulmón
Descritor malformación adenomatoide quística congénita del pulmón
Termo(s) alternativo(s) malformación adenomatoide quística congénita
Nota de escopo: 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.
Descritor em francês: Malformation congénitale kystique adénomatoïde du poumon
Termo(s) alternativo(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
Código(s) hierárquico(s): C08.381.150
C08.695.290
C16.131.740.290
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D015615
Nota de escopo: 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.
Nota de indexação: do not use / congen & do not coordinate with INFANT, NEWBORN, DISEASES
Qualificadores permitidos: 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
Indexação Anterior: Lung/abnormalities (1966-1989)
Nota MeSH pública: 90
Nota histórica: 90
Versão alternativa: CCAM
Identificador DeCS: 24597
ID do descritor: D015615
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1990
Data de entrada: 07/04/1989
Data de revisão: 09/07/2013
Cystic Adenomatoid Malformation of Lung, Congenital - Conceito preferido
Identificador do conceito M0023957
Nota de escopo 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.
Termo preferido Cystic Adenomatoid Malformation of Lung, Congenital
Termo(s) alternativo(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 - Mais específico
Identificador do conceito M0518873
Nota de escopo This type is characterized by a bulky solid mass with cysts of <0.5 cm.
Termo preferido Congenital Cystic Adenomatoid Malformation, Type III
Termo(s) alternativo(s) Congenital Cystic Adenomatoid Malformation, Type 3
Congenital Cystic Adenomatoid Malformation, Type I - Mais específico
Identificador do conceito M0518871
Nota de escopo This type is macrocystic, characterized by a single or multiple cysts of >2.5 cm.
Termo preferido Congenital Cystic Adenomatoid Malformation, Type I
Termo(s) alternativo(s) Congenital Cystic Adenomatoid Malformation, Type 1
Congenital Cystic Adenomatoid Malformation, Type II - Mais específico
Identificador do conceito M0518872
Nota de escopo This type is microcystic, characterized by multiple cysts of 0.5 to 2.5 cm.
Termo preferido Congenital Cystic Adenomatoid Malformation, Type II
Termo(s) alternativo(s) Congenital Cystic Adenomatoid Malformation, Type 2



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