极低出生体重儿胃裂的处理:病例报告。

IF 0.7 Q4 SURGERY
Noboru Oyachi, Fuminori Numano, Tamao Shinohara, Yasushi Murakami, Atsushi Nemoto, Atsushi Naito
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引用次数: 0

摘要

背景:胃裂是一种罕见的先天性畸形,腹腔脏器通过腹壁缺损疝出。由于极低出生体重儿(ELBW)的生理机能尚未发育成熟,并发症的风险增加,因此治疗极低出生体重儿的胃螺裂是一项重大挑战:本报告讨论的病例是一名在妊娠 29 周时通过紧急剖腹产出生的 ELBW 女婴,体重 768 克,产前诊断为胃裂。产后管理包括立即进行外科干预,使用膨体聚四氟乙烯(ePTFE)板手工制造的筒仓,将其缝合在患者的腹壁上,以适应其狭小的腹腔并保护肠系膜血流。坏死性小肠结肠炎并发肠穿孔,因此需要切除一段 10 厘米长的回肠并进行回肠造口术。婴儿体重增加不足,肝功能也出现障碍。不过,她最终在出生后第 142 天出院,体重 2774 克,口服喂养,未出现明显并发症:本病例强调了早产对患者临床结果的重大影响,并突出了个体化管理策略的重要性。我们的经验表明,根据腹部缺损情况定制筒仓的大小是可行的,同时也强调了对患有胃裂孔的 ELBW 婴儿优先考虑产后肠道灌注的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of gastroschisis in an extremely low birth weight infant: report of a case.

Background: Gastroschisis is a rare congenital anomaly in which abdominal organs herniate through a defect in the abdominal wall. Managing gastroschisis in extremely low birth weight (ELBW) infants presents significant challenges because of their immature physiologies and increased risk of complications.

Case presentation: This report discusses the case of a female ELBW infant born via an emergency cesarean section at 29 weeks of gestation, weighing 768 g, who had a prenatal diagnosis of gastroschisis. Postnatal management included immediate surgical intervention using a hand-made silo manufactured from expanded polytetrafluoroethylene (ePTFE) sheets that were sutured to the patient's abdominal wall to accommodate her small abdominal cavity and preserve mesenteric blood flow. Necrotizing enterocolitis with bowel perforation emerged as a complication, which led to the excision of a 10 cm segment of the ileum and the creation of an ileostomy. The infant experienced insufficient weight gain and liver dysfunction. However, she was eventually discharged on day 142 of life, weighing 2774 g, on oral feeding, without significant complications.

Conclusions: This case emphasizes how prematurity significantly affected the patient's clinical outcomes, and highlights the importance of individualized management strategies. Our experience demonstrates that custom silo placement allows for the size to be adapted to the abdominal defect, and highlights the critical need to prioritize postnatal bowel perfusion in ELBW infants with gastroschisis.

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