A case of isolated malrotation without midgut volvulus diagnosed prenatally and treated by laparoscopic surgery.

IF 0.7 Q4 SURGERY
Kosuke Endo, Hiroaki Fukuzawa, Yumi Mizoue, Atsushi Higashio, Mari Sonoda, Tamaki Iwade, Masahito Sato
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Abstract

Background: Malrotation is a congenital condition that predisposes individuals to midgut volvulus, which can result in significant bowel resection. While most cases of malrotation are diagnosed by the age of 1 year, typically presenting with symptoms related to volvulus or bowel obstruction, some cases remain asymptomatic. In children with visceral malposition, gastroschisis, omphalocele, or diaphragmatic hernia, malrotation may be suspected before symptoms manifest. However, isolated malrotation without midgut volvulus diagnosed prenatally is rare. We herein present a case of isolated malrotation without midgut volvulus that was prenatally diagnosed and successfully treated with laparoscopic surgery.

Case presentation: A 30-year-old woman (gravida 3, para 1) underwent routine obstetric ultrasound, which revealed increased blood flow in the lower uterine segment and abnormal placental attachment. To rule out placenta percreta, magnetic resonance imaging was performed at 34 weeks of gestation. Incidentally, abnormal fetal intestinal arrangement was noted, with the colon localized in the left hemi-abdomen and the small intestine distributed in the right hemi-abdomen, raising suspicion of malrotation. Postnatal contrast studies confirmed the diagnosis of malrotation without midgut volvulus. Given the risk of midgut volvulus, a laparoscopic Ladd's procedure was performed on day 6 of life. The postoperative course was uneventful, and the patient was still symptom-free 1 year postoperatively.

Conclusions: This case illustrates that malrotation can be prenatally diagnosed using fetal magnetic resonance imaging. Considering the risk of midgut volvulus, prophylactic Ladd's procedure should be performed in neonatal period. In cases where malrotation is not complicated by midgut volvulus, a laparoscopic Ladd procedure can be safely performed in neonates.

一例产前确诊的孤立性肠道旋转不良,但无中肠翻卷,经腹腔镜手术治疗。
背景:肠旋转不良是一种先天性疾病,易导致中肠翻卷,从而导致大肠切除。虽然大多数肠旋转不良病例在 1 岁前就能确诊,通常会出现与肠旋转或肠梗阻相关的症状,但有些病例仍无症状。对于内脏位置不正、胃裂、脐疝或膈疝的患儿,在出现症状之前就可能怀疑有旋转不良。然而,产前确诊的孤立性肠管旋转不良而无中肠翻卷的病例并不多见。我们在此介绍一例产前诊断为孤立性肠管旋转不良但无中肠翻卷的病例,并通过腹腔镜手术成功治疗了该病:病例介绍:一名 30 岁的妇女(孕 3,1 段)接受了常规产科超声波检查,结果显示子宫下段血流增加,胎盘附着异常。为排除胎盘早剥的可能,在妊娠 34 周时进行了磁共振成像检查。偶然发现胎儿肠道排列异常,结肠位于左半腹,小肠分布在右半腹,因此怀疑是肠旋转不良。出生后的造影检查证实了肠旋转不良的诊断,但没有中肠翻卷。考虑到中肠翻卷的风险,在婴儿出生后第 6 天为其实施了腹腔镜拉德氏手术。术后过程顺利,患者术后一年仍无症状:本病例说明,胎儿磁共振成像可以在产前诊断出肠管旋转不良。考虑到中肠旋转的风险,应在新生儿期进行预防性拉德氏手术。如果旋转不良没有并发中肠翻卷,则可以在新生儿中安全地进行腹腔镜拉德氏手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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13 weeks
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