一名足月新生儿术后超短肠综合征:一年随访

Q4 Medicine
Kaushaki Shankar, Bhavya Kukreja, Harsh Wardhan, Vipul Saneja, Vishnu Dutta Agrawal
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引用次数: 0

摘要

超短肠综合征是指小肠长度低于 10-25 厘米,或低于同龄人预期长度的 10%。超短肠综合症在新生儿中很少发生,但一旦发生,就会导致很高的发病率和死亡率。由于营养吸收不良,存活下来的新生儿在生长发育方面会受到严重影响。多学科方法和积极的肠外营养是治疗的主要手段。我们的病例在出生 20 天时出现肠旋转不良和中肠倒流,导致术后超短肠综合征。尽管婴儿只剩下 20 厘米长的短肠,但经过保守治疗后仍存活了下来,并且生长发育良好;婴儿从 11 个月大开始就完全脱离了肠外营养。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-operative Ultrashort Bowel Syndrome in a Term Neonate: One-year Follow-up
Ultrashort bowel syndrome occurs when the length of the small bowel is below 10–25 cm, or 10% of that expected for age. It is a rare occurrence in neonates; however, when it occurs, it results in high morbidity and mortality. Surviving newborns face a significant detriment in growth and development due to malabsorption of nutrients. A multidisciplinary approach with aggressive parenteral nutrition is the mainstay of management. Our case presented at 20 days of life, with malrotation and midgut volvulus resulting in post-surgical ultrashort bowel syndrome. In spite of being left with only 20 cm of short bowel, the infant survived on conservative management and is thriving well; the infant has been off parenteral nutrition completely since 11 months of age.
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来源期刊
Journal of Neonatology
Journal of Neonatology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
55
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