| Literature DB >> 25926923 |
Damien Pike1, Sindu Mohan2, Weijing Ma3, James F Lewis4, Grace Parraga5.
Abstract
Congenital lobar emphysema is mainly diagnosed in infants, although rare cases are reported in adults. A 20-yr-old female with acute dyspnea, chest pain and left upper lobe (LUL) chest x-ray hyperlucency underwent 3He magnetic resonance imaging (MRI) for ventilation and apparent diffusion coefficient (ADC) measurements, as well as CT for emphysema and airway wall measurements. Forced expiratory volume in 1s, residual volume, and airways-resistance were abnormal, but there was normal carbon-monoxide-diffusing-capacity. The LUL relative area of the density histogram <-950 HU and airway morphology were highly abnormal compared with the other lobes and coincident with highly abnormal MRI-derived acinar duct dimensions. CT also identified bronchial atresia and congenital lobar emphysema as the source of symptoms in this case where there was also functional imaging evidence of collateral ventilation from the fissure (and not the abnormally terminated airway) into the emphysematous LUL.Entities:
Keywords: Airways Disease; Bronchial Atresia; Computed Tomography; Congenital Lobar Emphysema; Emphysema; Hyperpolarized 3He; Magnetic Resonance Imaging
Mesh:
Year: 2015 PMID: 25926923 PMCID: PMC4391802 DOI: 10.3941/jrcr.v9i2.2048
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922