先天性胃肠道及肾脏合并畸形1例

S. V. Aborin, D. V. Pechkurov, A. V. Varlamov, A. V. Maznova, N. V. Sviridova
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引用次数: 0

摘要

目前,儿童先天性畸形的矫治是现代医学的重要任务之一。如果及时根治缺陷,孩子将健康成长。先天性畸形的组合给临床医生带来了严重的困难,需要多学科团队的参与,结合各种途径和方法。本文报告一新生儿回肠闭锁、主动脉弓发育不全及双侧肾脏发育不全的临床病例。自出生以来,孩子的病情因休克和随后的氮质血症、水合过度而变得复杂。由于闭锁的矫正不能拖太久,所以决定手术中在肠上植入腹膜导尿管,以防急性肾损伤反复发作。本临床病例证明了在腹腔手术后患者进行肾脏替代治疗的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination of congenital malformation of the gastrointestinal tract and kidneys: a clinical case
Currently, the correction of congenital malformations in children is one of the important tasks of modern medicine. If a radical correction of the defect is performed timely, the child will grow up healthy. Combinations of congenital malformations create serious difficulties for clinicians and require the participation of a multidisciplinary team, combining various approaches and methods. The article presents a clinical case of a newborn child with atresia of the ileum, hypoplasia of the aortic arch and bilateral hypoplasia of the kidneys. Since birth, the child’s condition was complicated by the development of shock and subsequent azotemia, hyperhydration. Since the correction of atresia could not be postponed for a long time, it was decided to perform implantation of a peritoneal catheter during surgery on the intestine in case of a repeat episode of acute kidney injury. The presented clinical case demonstrates the possibility of renal replacement therapy in patients after surgery in the abdominal cavity.
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