Cystic Adenomatoid Malformation of Lung, Congenital
"Cystic Adenomatoid Malformation of Lung, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
Descriptor ID |
D015615
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MeSH Number(s) |
C08.381.150 C08.695.290 C16.131.740.290
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Concept/Terms |
Cystic Adenomatoid Malformation of Lung, Congenital- Cystic Adenomatoid Malformation of Lung, Congenital
- Congenital Cystic Adenomatoid Malformation of Lung
- Lung Malformation, Congenital Cystic Adenomatoid
- Lung Malformation, Cystic Adenomatoid, Congenital
- Congenital Cystic Adenomatoid Malformation
- Cystic Adenomatoid Malformation of Lung
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Below are MeSH descriptors whose meaning is more general than "Cystic Adenomatoid Malformation of Lung, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Cystic Adenomatoid Malformation of Lung, Congenital".
This graph shows the total number of publications written about "Cystic Adenomatoid Malformation of Lung, Congenital" by people in UAMS Profiles by year, and whether "Cystic Adenomatoid Malformation of Lung, Congenital" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2018 | 1 | 0 | 1 | 1996 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cystic Adenomatoid Malformation of Lung, Congenital" by people in Profiles over the past ten years.
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Vandewalle RJ, Easton JC, Burns RC, Gray BW, Rescorla FJ. Review of Early Postoperative Metrics for Children Undergoing Resection of Congenital Pulmonary Airway Malformations and Report of Pleuropulmonary Blastoma at a Single Institution. Eur J Pediatr Surg. 2019 Oct; 29(5):417-424.
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