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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
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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 |
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Código(s) hierárquico(s): |
C08.381.150 C08.695.290 C16.131.740.290 |
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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. |
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Nota de indexação: | do not use / congen & do not coordinate with INFANT, NEWBORN, DISEASES |
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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 |
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Indexação Anterior: |
Lung/abnormalities (1966-1989) |
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Nota MeSH pública: | 90 |
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Nota histórica: | 90 |
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Versão alternativa: | CCAM |
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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 |
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Cystic Adenomatoid Malformation of Lung, Congenital
- Conceito preferido
Congenital Cystic Adenomatoid Malformation, Type III
- Mais específico
Congenital Cystic Adenomatoid Malformation, Type I
- Mais específico
Congenital Cystic Adenomatoid Malformation, Type II
- Mais específico
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 |
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 |
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 |
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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