Abstract | INTRODUCTION: Swyer-James-MacLeod syndrome or unilateral hyperlucent lung syndrome is a rare entity associated with postinfectious bronchiolitis obliterans occurring in childhood. It is characterized by hypoplasia and/or agenesis of the pulmonary arteries resulting in pulmonary parenchyma hypoperfusion. CASE PRESENTATION: Here we report the case of a 53-year-old Caucasian woman with Swyer-James-MacLeod syndrome found in the differential diagnosis workup for a new onset of heart failure, secondary to pulmonary arterial hypertension complicated by a patent ductus arteriosus. CONCLUSION: Typically, this disorder is diagnosed in childhood after evaluation for recurrent respiratory infections, but sometimes an indolent course means diagnosis is not made until adulthood.
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Authors | Carlos Capela, Paulo Gouveia, Marco Sousa, Maria J Regadas |
Journal | Journal of medical case reports
(J Med Case Rep)
Vol. 5
Pg. 2
(Jan 04 2011)
ISSN: 1752-1947 [Electronic] England |
PMID | 21205288
(Publication Type: Journal Article)
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