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Horseshoe lung associated with left-lung hypoplasia, left pulmonary artery sling and bilateral agenesis of upper lobe bronchi

机译:马蹄肺伴左肺发育不全,左肺动脉吊带和上叶支气管双侧发育不全

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摘要

Horseshoe lung, a rare congenital anomaly, is almost always associated with unilateral (usually right-sided) lung hypoplasia, and, in most cases, in conjunction with the scimitar syndrome. We present an 8-month-old boy with horseshoe lung associated with left-lung hypoplasia, left pulmonary artery sling and bilateral agenesis of the upper lobe bronchi, diagnosed by multidetector CT (MDCT) imaging. The study also revealed an anomalous origin of the left vertebral artery as the last branch of the aortic arch, distal to the left subclavian artery, and an anomalous origin of the left common carotid artery from the brachiocephalic trunk. A hemivertebral anomaly of the seventh cervical vertebra was incidentally detected. MDCT with high-quality multiplanar and three-dimensional reconstructions is a noninvasive and rapid technique for detecting the complex combination of vascular, tracheobronchial and parenchymal anomalies, and any potential bone anomalies, in one imaging study.
机译:马蹄形肺是一种罕见的先天性异常,几乎总是与单侧(通常为右侧)的肺发育不全有关,在大多数情况下,还与弯刀综合症有关。我们提出了一个8个月大的男孩,患有马蹄肺,伴有左肺发育不全,左肺动脉悬吊和上叶支气管双侧发育不全,经多探测器CT(MDCT)成像诊断。该研究还揭示了左椎动脉的异常起源是主动脉弓的最后分支,位于左锁骨下动脉远端,而左颈总动脉的异常起源则来自头臂干。偶然发现第七个颈椎的半椎异常。具有高质量多平面和三维重建的MDCT是一项无创且快速的技术,可在一项影像学研究中检测血管,气管支气管和实质异常以及任何潜在的骨骼异常的复杂组合。

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