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伴有完全性内脏反位的VACTERL综合征:一种独特的组合。

VACTERL Association with Situs Inversus Totalis: A Unique Combination.

作者信息

Slagle Cara L, Schulz Elizabeth V, Annibale David J

出版信息

Neonatal Netw. 2019 Mar 1;38(2):98-106. doi: 10.1891/0730-0832.38.2.98. Epub 2019 Mar 6.

Abstract

BACKGROUND

VACTERL association is a sporadic, nonrandom series of congenital malformations diagnosed by the presence of three or more of the following: vertebral malformations, anal atresia, cardiac defects, tracheoesophageal fistula, renal malformations, and limb malformations. Situs inversus totalis (SIT) and esophageal malformations are rarely associated. This is the first reported case in North America of VACTERL association with SIT.

IMPLICATIONS FOR PRACTICE

Respiratory distress in the term infant requires full exploration of all possible causes because the etiology may be far more complex than routinely diagnosed respiratory distress syndrome. This particular case demonstrates physical exam findings and supportive imaging that would be observed in infants with VACTERL association and with SIT, highlighting considerations when, rarely, both occur simultaneously.

摘要

背景

VACTERL综合征是一种散发性、非随机性的先天性畸形组合,通过以下三种或更多畸形的存在来诊断:脊柱畸形、肛门闭锁、心脏缺陷、气管食管瘘、肾脏畸形和肢体畸形。全内脏转位(SIT)和食管畸形很少与之相关。这是北美首例报道的VACTERL综合征合并SIT的病例。

对临床实践的启示

足月儿的呼吸窘迫需要全面探究所有可能的病因,因为其病因可能比常规诊断的呼吸窘迫综合征更为复杂。这个特殊病例展示了VACTERL综合征合并SIT的婴儿的体格检查结果和辅助影像学表现,突出了这两种情况罕见同时发生时的注意事项。

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