| Literature DB >> 28567181 |
Humza Mahmood1, Andrew Plumb2, Roser Vega3, Alastair Windsor3.
Abstract
Pulmonary sequestration (PMS) is a rare bronchopulmonary malformation. It has an incidence of between 0.15% to 1.7%. Likewise, cystic adenomatoid malformation (CCAM) is another relatively rare category of a bronchopulmonary malformation with a reported incidence of between 1 in 25,000 to 1 in 35,000. Moreover, a bronchopulmonary malformation with features allied to both of these forms is considered an even rarer entity. In general, bronchopulmonary malformations present with a range of non-specific symptoms. Radiological features can be non-specific yet distinctive when related to clinical features. Ultimately, definitive diagnosis depends upon histological assessment of lung tissue. We present an adult female with radiological features of both pulmonary sequestration and cystic adenomatoid malformation. This was an incidental finding unrelated to the patients presenting complaint. This case highlights the importance of using a structured and systematic approach when interpreting medical imagery.Entities:
Keywords: bronchopulmonary foregut malformation; congenital cystic adenomatoid malformation; extralobar pulmonary sequestration; intralobar pulmonary sequestration; pulmonary sequestration
Mesh:
Year: 2017 PMID: 28567181 PMCID: PMC5439451 DOI: 10.3941/jrcr.v11i4.3002
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922