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内脏异位中的肠道旋转和固定异常:早期检测与管理

Intestinal rotation and fixation abnormalities in heterotaxia: early detection and management.

作者信息

Chang J, Brueckner M, Touloukian R J

机构信息

Section of Pediatric Surgery, Yale-New Haven Hospital, CT.

出版信息

J Pediatr Surg. 1993 Oct;28(10):1281-4; discussion 1285. doi: 10.1016/s0022-3468(05)80313-6.

DOI:10.1016/s0022-3468(05)80313-6
PMID:8263687
Abstract

Intestinal rotation and fixation abnormalities (IRFA) are known to coexist with heterotaxia (defined as an abnormal arrangement of body organs that is different from complete situs solitus or complete situs inversus), but little is known about the incidence of this association or its clinical management. We have reviewed the records of 34 patients diagnosed with heterotaxia during a 12-year period at Yale-New Haven Hospital in order to develop a plan for the early diagnosis of IRFA and to assess the value of preventive treatment in this complicated group of patients. Of the 34 patients with heterotaxia, all except one presented with complex congenital heart disease. The 34 patients were divided into two groups on the basis of their gastrointestinal workup for suspected IRFA. The 28 patients in group A had no upper gastrointestinal (GI) contrast study performed prior to symptoms suggestive of IRFA. Four of these 28 patients (14%) eventually developed complications of IRFA requiring emergency surgery. Group B consisted of six patients seen during the past 5 years with heterotaxia who had upper GI contrast studies while asymptomatic. All six (100%) were shown to have IRFA and subsequently underwent an uncomplicated elective Ladd procedure once their cardiac condition stabilized. This study confirms the high incidence of IRFA in patients with heterotaxia. We propose that evaluating patients with heterotaxia syndrome for IRFA while asymptomatic may prevent the need for emergency abdominal surgery in patients that have major cardiovascular anomalies.

摘要

已知肠道旋转和固定异常(IRFA)与内脏异位(定义为身体器官的异常排列,不同于完全正常位或完全反位)并存,但对于这种关联的发生率及其临床管理知之甚少。我们回顾了耶鲁-纽黑文医院12年间诊断为内脏异位的34例患者的记录,以便制定IRFA的早期诊断计划,并评估在这组复杂患者中进行预防性治疗的价值。在34例内脏异位患者中,除1例之外均患有复杂先天性心脏病。根据对疑似IRFA的胃肠道检查结果,将这34例患者分为两组。A组的28例患者在出现提示IRFA的症状之前未进行上消化道(GI)造影检查。这28例患者中有4例(14%)最终出现IRFA并发症,需要进行急诊手术。B组由过去5年中诊断为内脏异位的6例无症状患者组成,他们进行了上消化道造影检查。所有6例(100%)均显示有IRFA,随后在心脏状况稳定后接受了无并发症的择期Ladd手术。这项研究证实了内脏异位患者中IRFA的高发生率。我们建议,对内脏异位综合征患者在无症状时进行IRFA评估,可能会避免有严重心血管异常的患者进行急诊腹部手术。

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A study of associated congenital anomalies with biliary atresia.一项关于胆道闭锁相关先天性异常的研究。
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Early versus delayed surgical correction of malrotation in children with critical congenital heart disease.
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