Descriptor English: | Cystic Adenomatoid Malformation of Lung, Congenital | ||||||
Descriptor Spanish: |
Malformación Adenomatoide Quística Congénita del Pulmón
| ||||||
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
Congenital Cystic Adenomatoid Malformation, Type III
- Narrower
Congenital Cystic Adenomatoid Malformation, Type I
- Narrower
Congenital Cystic Adenomatoid Malformation, Type II
- Narrower
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 |
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 |
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 |
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 |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey