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先天性喘鸣:主动脉缩窄的罕见表现。

Congenital stridor: unusual manifestation of coarctation of the aorta.

作者信息

Park J G, Wylam M E

机构信息

Division of Pulmonary and Critical Care Medicine, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, Minnesota, 55905, USA.

Division of Adult and Pediatric Pulmonary and Critical Care Medicine, Mayo Clinic College of Medicine, 200 First Street, SW, Rochester, Minnesota, 55905, USA.

出版信息

Pediatr Cardiol. 2006 Jan-Feb;27(1):137-139. doi: 10.1007/s00246-005-1066-5.

Abstract

Coarctation of the aorta is a relatively common congenital condition. Most infantile presentations of aortic coarctation are related to the associated congenital cardiac abnormalities leading to congestive heart failure or systemic hypoperfusion. We describe a 4-month-old infant who presented with stridor as the sole manifestation of coarctation. Radiologic studies revealed enlarged innominate artery due to the aortic coarctation that resulted in tracheal compression. After surgical correction, respiratory signs and symptoms completely resolved. This case report describes a unique cause of stridor in newborn infants and discusses the potential for vascular anomalies to result in tracheal narrowing.

摘要

主动脉缩窄是一种相对常见的先天性疾病。大多数婴儿期主动脉缩窄的表现与相关的先天性心脏异常有关,可导致充血性心力衰竭或全身灌注不足。我们描述了一名4个月大的婴儿,其仅以喘鸣为主动脉缩窄的唯一表现。影像学研究显示,由于主动脉缩窄导致无名动脉增粗,进而压迫气管。手术矫正后,呼吸体征和症状完全消失。本病例报告描述了新生儿喘鸣的一种独特病因,并讨论了血管异常导致气管狭窄的可能性。

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