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http://www.scirp.org/journal/PaperInformation.aspx?PaperID=53974#.VN2umCzQrzE
Affiliation(s)
1The Division of Cardiothoracic Surgery, Veterans Affairs Medical Center, Portland, USA.
2The George Washington University, Washington DC, USA.
2The George Washington University, Washington DC, USA.
ABSTRACT
Swyer-James-MacLeod
syndrome is a rare disease that results in parenchymal damage believed
to be caused by recurrent lung infections in childhood. We report a case
of a previously healthy young woman that presented with insidious
progression of exertional dyspnea with restrictive lung physiology.
Axial imaging demonstrated a hyperinflated emphysematous right lung with
lower lobe fibrosis, nodules and air-fluid filled cysts, with a small
right pulmonary artery and contralateral shifting of the mediastinum.
She underwent right pneumonectomy ultimately resultingin improvement of
her symptoms, with surgical pathology indicating extensive
emphysema,bronchiec- tasis, fibrosis with osseous metaplasia, and
placental transmogrification of alveolar septa, being consistent with a
diagnosis of SJMS.
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References
Cruz, M. and Trachiotis, G. (2015) Pneumonectomy in a Patient with Swyer-James-MacLeod Syndrome. Surgical Science, 6, 55-58. doi: 10.4236/ss.2015.62009.
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