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马蹄肺合并左肺发育不全、左肺动脉吊带及双侧上叶支气管缺如。

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

作者信息

Oguz Berna, Alan Serdar, Ozcelik Ugur, Haliloglu Mithat

机构信息

Department of Radiology, Hacettepe University Faculty of Medicine, Ankara 06100, Turkey.

出版信息

Pediatr Radiol. 2009 Sep;39(9):1002-5. doi: 10.1007/s00247-009-1300-z. Epub 2009 May 21.

Abstract

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.

摘要

马蹄肺是一种罕见的先天性异常,几乎总是与单侧(通常为右侧)肺发育不全相关,并且在大多数情况下,与弯刀综合征并存。我们报告一名8个月大的男孩,患有与左肺发育不全、左肺动脉吊带和双侧上叶支气管缺如相关的马蹄肺,通过多排螺旋CT(MDCT)成像诊断。该研究还显示左椎动脉异常起源于主动脉弓的最后一个分支,位于左锁骨下动脉远端,左颈总动脉异常起源于头臂干。偶然发现第七颈椎半椎体异常。具有高质量多平面和三维重建的MDCT是一种无创且快速的技术,可在一次成像研究中检测血管、气管支气管和实质异常以及任何潜在骨异常的复杂组合。

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