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眼耳脊椎发育异常中的先天性心脏、肺部和血管畸形。

Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia.

作者信息

Pierpont M E, Moller J H, Gorlin R J, Edwards J E

出版信息

Pediatr Cardiol. 1982;2(4):297-302. doi: 10.1007/BF02426976.

Abstract

Three cases of oculoauriculovertebral dysplasia (OAV) with associated cardiac, pulmonary, and facial malformations are described. One patient had a rare condition: isolation of the left innominate artery. All 3 had pulmonary anomalies ranging from minor (incomplete lobulation) to major (hypoplasia of the left lung). When pulmonary hypoplasia occurs, it is usually on the same side of the body as the facial anomalies. Forty-five reported cases of OAV with associated cardiac, vascular, and pulmonary abnormalities are reviewed. Tetralogy of Fallot and ventricular septal defect account for half of the cardiac malformations. In the remaining cases, a wide variety of cardiovascular malformations are present. It is suggested that the facial malformations in OAV may result from a perfusion abnormality. An isolated left innominate artery (as in one of our cases) could produce abnormal vascular supply to the external carotid artery and the facial structures that it supplies.

摘要

本文描述了三例伴有心脏、肺部和面部畸形的眼耳脊椎发育异常(OAV)病例。其中一名患者患有罕见病症:左无名动脉孤立。所有三名患者均有肺部异常,从轻微(不完全分叶)到严重(左肺发育不全)不等。当发生肺发育不全时,通常与身体同侧的面部畸形相关。本文回顾了45例伴有心脏、血管和肺部异常的OAV报告病例。法洛四联症和室间隔缺损占心脏畸形的一半。在其余病例中,存在各种各样的心血管畸形。提示OAV中的面部畸形可能由灌注异常引起。孤立的左无名动脉(如我们的一例病例)可能导致颈外动脉及其所供应的面部结构的异常血管供应。

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