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Interact CardioVasc Thorac Surg 2009;8:484. doi:10.1510/icvts.2008.197566B © 2009 European Association of Cardio-Thoracic Surgery
eComment: Diagnostic and surgical considerations in Swyer–James–MacLeod syndromeThoracic Surgery Department, Theagenio Hospital, A. Simeonidi 2, 54007 Thessaloniki, Greece Swyer–James–MacLeod syndrome; repeated chest drainages in apatient misdiagnosed with pneumothorax We read with great interest the article by Sulaiman et al. [1] regarding a case of a patient with Swyer–James–McLeod syndrome and we would like to congratulate them and highlight a few points. Swyer–James–MacLeod syndrome is morphologically characterized by the presence of constrictive bronchiolitis with dilatation and destruction of alveolar structures, resulting in significant air trapping and lung hypoperfusion. The main pathogenetic factor seems to be acute bronchiolitis with obliteration of small airway in childhood [2]. Ventilation perfusion (VQ) scan is very helpful in determining the extent of the disease and correlates well with high resolution computed tomography (HCRT) which seems to be the most valuable technique. The volume and antero-posterior attenuation gradient of the affected lung, size and distribution of central and peripheral pulmonary arteries, air trapping, the patency of main airways and presence of bronchiectasis are investigated. The appearance of the lungs on forced expiration is important in the assessment of Swyer–James–MacLeod syndrome with HCRT and therefore the patient's cooperation is essential. The patient should be placed in the prone position to help identify the typical mosaic pattern of the syndrome. Surgical treatment is predicated upon the principle that a reduction in lung volume can favorably affect the mechanics of the diaphragm, chest wall and airways. Video-assisted thoracic surgery techniques could be very useful and effective [2].
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