罕见的回肠闭锁1例

Aniket Agrawal
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引用次数: 0

摘要

背景:先天性心血管异常是儿童发病和死亡的重要原因。胃肠道系统问题在先天性心血管异常患者中并不罕见。这些胃肠道问题既与先天性缺陷有关,也可能由于使用体外循环治疗这些问题而发生,这可能导致再分配,从而导致血流减少,导致缺血。1例:男婴,出生25天,产前诊断为先天性心脏缺陷,产后超声诊断为混合性不规则TAPVC伴前肌室间隔缺损(VSD)。TAPVC改道矫正完成后,在术后第3天,患儿出现腹胀,并进行了儿科外科转诊。经检查,孩子有发烧、心动过速和肠音迟缓。影像学提示肠梗阻,予以保守处理。病人后来开始口服感觉,但不能很好地耐受因此计划进行探查性剖腹手术发现远端回肠闭锁。该畸形在同一手术中得到纠正,术后过程平稳。结论:综上所述,即使有排便史的新生儿,回肠闭锁仍应被视为鉴别之一,特别是在排除了常见的情况后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Unusual Case Of Ileal Atresia: A Case Report
Background: Congenital cardiovascular abnormalities are an important cause of morbidity and mortality in the pediatric age group. GI system problems are not uncommon in patients with congenital cardiovascular abnormalities. These GI problems include both that are associated with the congenital defect, or they may occur due to cardiopulmonary bypass use to treat these problems, which can cause a redistribution and thus a decrease in blood flow leading to ischemia. Case: Male child, 25 days of life, was antenatally diagnosed to have a congenital heart defect, which on post-natal ECHO was diagnosed as Mixed Anamolous TAPVC with an Anterior Muscular Ventricular Septal Defect (VSD). After the TAPVC re-routing correction was done, on post-op day 3, the child developed abdominal distension and a pediatric surgical referral was taken. On examination, the child had fever, tachycardia and sluggish bowel sounds. Imaging suggested ileus which was managed conservatively. Patient was later started on oral feels which were not tolerated well so an exploratory laparotomy was planned which revealed distal ileal atresia. The anomaly was corrected in the same surgery and post-op course was uneventful. Conclusion: To summarize everything that has been stated so far, in neonates even with the history of stool passage, ileal atresia should still be considered as one of the differentials, particularly after the common ones have been ruled out.
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