Seven years after surgical correction of Scimitar syndrome, a 19-year-old patient complained of progressive dyspnea and tachycardia. Transthoracic echocardiography revealed a mass compressing the right ventricle. Magnetic resonance tomogram showed its exact retrosternal location and nature. A computed tomography-guided drainage decompressed the mass. Because of cystic wall persistence, a surgical extirpation of the whole cystic cavity was deemed necessary.
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| http://dx.doi.org/10.1111/j.1540-8191.2008.00613.x | DOI Listing |
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