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The Annals of Thoracic Surgery, Vol 56, 120-124, Copyright © 1993 by The Society of Thoracic Surgeons
SK Ohri, G Rutty and SW Fountain
Three cases of Macleod's syndrome are described, all of which required
surgical resections for distressing symptoms. This provided a rare
opportunity to examine the pathologic features of a condition that is
usually diagnosed on its radiologic features, and the etiology of which
remains unestablished. Three patients (2 women and 1 man), aged 20, 23, and
24 years, were referred from respiratory physicians because of unilateral
hyperlucent lungs and associated symptoms. All 3 patients had unilateral
hyperlucent lungs, but only 1 patient had demonstrable mediastinal shift on
expiratory and inspiratory chest computed tomographic scan. Segmentectomies
were performed (n = 4) in all the patients without perioperative morbidity
or mortality. Patients have been followed up between 6 and 18 months, and
remain asymptomatic with a return to normal lifestyle. Histologic
examination of the specimens found inflammation of the bronchus in all 3
patients, but only two specimens had evidence of bronchiolar inflammation.
In only 1 patient was there a reduction in bronchiole number. All 3
patients showed presence of emphysema. These cases are notable for the
segmental distribution of the disease. Pathologic examination lends support
to the theory that previous respiratory tract infection may play a role in
the pathogenesis of this condition.
ARTICLES
Acquired segmental emphysema: the enlarging spectrum of Swyer- James/Macleod's syndrome
Thoracic Surgical Unit, Harefield Hospital, United Kingdom.
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