Pulmonary MR Angiography in Swyer-James Syndrome
نویسندگان
چکیده
Aim: The aim of this study was to investigate the pulmonary magnetic resonance angiography (MRA) imaging findings in Swyer – James syndrome (SJS) as a alternative imaging modalities. Methods: Thirteen patients had posteroanterior inspiratory/expiratory chest X-ray films and pulmonary MRA with SJS (6 males, 7 females) were retrospectively studied. Gradient-echo pulmonary MRA was performed in all patients with a 1.5 T MR unit. MRA imaging was performed in a single breath-hold during the injection of contrast media. Image analysis of the patients was performed. The results of pulmonary artery diameters and pulmonary peripheral vasculature were compared between normal sides versus the affected sides. Statistical analysis was performed with the Student t test. Results: The smaller pulmonary artery on the affected side with poor peripheral vasculature was observed with gadolinium-enhanced gradient-echo MRA in all patients. There was a significant difference between the diameters of the pulmonary arteries of the normal versus the disease sides (p< 0.0005). Conclusion: MRA successfully depicted the small pulmonary artery with diminished peripheral vasculature in patients with SJS. This study showed the pulmonary MRA imaging could be used as a alternative imaging modalities in the evaluation of patient with SJS.
منابع مشابه
Swyer–james Syndrome: Demonstration by 64-slice 3d Mdct Angiography and Coronal Mpr Ct Imaging
Swyer – James syndrome (SJS) was first described by Swyer and James in a 6-year-old child in 1953 (1). The following year, MacLeod reported nine patients with unilateral pulmonary hyperlucency (2). SJS is a rare disease characterized by a hyperlucent lung or lobe, usually of normal or small size, associated with air trapping and diminutive pulmonary vascularization (3). Swyer-James syndrome app...
متن کاملSwyer-James syndrome associated with asthma and a giant bulla
Swyer-James syndrome was first described in 1953 as unilateral pulmonary emphysema in a 6-year-old boy. The characteristic feature of this syndrome is unilateral pulmonary hyperlucency on a chest X-ray film. Typical symptoms include recurrent chest infections, chronic cough, wheezing, and exertional dyspnea. Although there have been a few reports of pneumothorax in patients with Swyer-James syn...
متن کاملA persistent pneumothorax? 5-year follow-up after diagnosis of Swyer–James–MacLeod syndrome
Swyer-James-MacLeod syndrome should be considered in healthy patients with unilateral pulmonary hyperlucency http://ow.ly/YWps9.
متن کاملScimitar Syndrome: Pathology, Clinical Presentation, Radiographic Features, and Treatment
Scimitar syndrome is characterized by partial or total anomalous pulmonary venous return from the right lung along with pulmonary hypoplasia.Wesearched the mail databases such as Medline (via PubMed), Scopus and EMBASE and Google Scholar. Diagnosing infantile scimitar syndrome requires meticulous attention and high suspicion of the early referral and management. The association of the syndrome ...
متن کاملA case of Swyer-James-MacLeod syndrome diagnosed in adulthood.
Swyer-James-MacLeod syndrome (SJMS), or unilateral hyperlucent lung syndrome, is a rare disease thought to be associated with post-infectious bronchiolitis obliterans (1). This disease was first described in 1953 by Swyer and James in a 6-year-old child who had been treated with pneumonectomy (2). MacLeod presented a unilateral hyperlucency series one year later. From this date on, the disease ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2010