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完全性肺静脉异位引流与婴儿猝死

Total anomalous pulmonary venous drainage and sudden death in infancy.

作者信息

Byard R W, Moore L

机构信息

Department of Histopathology, Adelaide Children's Hospital, Australia.

出版信息

Forensic Sci Int. 1991 Oct;51(2):197-202. doi: 10.1016/0379-0738(91)90186-m.

Abstract

The clinicopathologic features of four infants with undiagnosed total anomalous pulmonary venous return who died suddenly and unexpectedly are presented. Two infants were found dead in their beds and two collapsed following very non-specific episodes of mild tachypnoea and tachycardia, respectively. Pulmonary venous blood drained via a common channel to the left innominate vein, the superior vena cava, the inferior vena cava at the junction of the hepatic vein and the supradiaphragmatic portion of the inferior vena cava. All cases demonstrated right atrial and ventricular hypertrophy and in one case there was associated hypoplastic left heart syndrome. Although those mechanisms responsible for sudden infant death syndrome could not definitely be excluded in two cases, the presence of anomalous pulmonary drainage with significant right-sided cardiac cardiac hypertrophy in each patient strongly suggests a contributing role for the vascular malformation in the aetiology of sudden unexpected death. The importance of careful in situ dissection of the major vessels in all cases of paediatric sudden death is emphasised, particularly in the presence of other congenital cardiac anomalies.

摘要

本文介绍了四名未确诊的完全性肺静脉异位引流婴儿的临床病理特征,这些婴儿均突然意外死亡。两名婴儿被发现死于床上,另外两名婴儿分别在出现非常不典型的轻度呼吸急促和心动过速发作后晕倒。肺静脉血通过一个共同通道引流至左无名静脉、上腔静脉、肝静脉与下腔静脉膈上部分交界处的下腔静脉。所有病例均表现为右心房和右心室肥大,其中一例合并左心发育不全综合征。虽然在两例中不能明确排除婴儿猝死综合征的相关机制,但每位患者均存在异常肺静脉引流并伴有明显的右心肥大,这强烈提示血管畸形在意外猝死病因中起一定作用。强调了在所有儿科猝死病例中仔细原位解剖主要血管的重要性,尤其是在存在其他先天性心脏异常的情况下。

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