Intussusception in Neonates: Uncommon Causes and Diagnostic Dilemmas in Two Case Reports.

IF 0.7 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastroenterology Pub Date : 2026-04-30 eCollection Date: 2026-01-01 DOI:10.1159/000552199
Salma Mani, Lamiri Rachida, Amine Ksia, Lassaad Sahnoun, Amani N Alansari
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引用次数: 0

Abstract

Introduction: Neonatal intussusception (NI), although a rare cause of bowel obstruction, presents significant diagnostic challenges due to its clinical heterogeneity. This report describes two cases of NI, both presenting with vomiting and hematochezia. In both instances, the initial radiological evaluations led to a misdiagnosis, delaying timely treatment. Surgical intervention ultimately confirmed the diagnosis in both cases, highlighting the limitations of imaging modalities in neonates.

Case presentations: In the first case, a full-term female neonate presented with bilious vomiting and rectal bleeding on day one of life. Despite suspicion of an intestinal duplication on ultrasonography, the definitive diagnosis was made intraoperatively, where ileocecal intussusception and colonic duplication were identified. In the second case, a full-term male neonate exhibited similar symptoms but with signs suggestive of volvulus on imaging. Surgical exploration revealed an ileocolonic intussusception, which was reduced manually without ischemia or necrosis.

Conclusion: These cases emphasize the rarity of NI and the importance of considering it in differential diagnoses of neonates presenting with acute gastrointestinal symptoms, particularly when radiological findings are inconclusive. Timely surgical intervention remains critical for definitive diagnosis and optimal outcomes. Pediatric surgeons and clinicians must maintain a high index of suspicion for this rare condition to ensure timely diagnosis and minimize associated morbidity and mortality.

新生儿肠套叠:两例罕见病因和诊断困境报告。
新生儿肠套叠(NI)虽然是一种罕见的肠梗阻原因,但由于其临床异质性,其诊断面临重大挑战。本报告描述两例NI病例,均表现为呕吐和便血。在这两个病例中,最初的放射学评估导致了误诊,延误了及时治疗。手术干预最终证实了这两例的诊断,强调了新生儿影像学的局限性。病例介绍:在第一个病例中,一个足月的女性新生儿在出生的第一天出现胆汁性呕吐和直肠出血。尽管超声检查怀疑有肠重复,但术中明确诊断为回盲肠套叠和结肠重复。在第二个病例中,一个足月男性新生儿表现出类似的症状,但影像学显示有扭转的迹象。手术探查发现回肠肠套叠,手工复位,无缺血坏死。结论:这些病例强调了NI的罕见性和在新生儿急性胃肠道症状的鉴别诊断中考虑它的重要性,特别是当影像学检查结果不确定时。及时的手术干预仍然是明确诊断和最佳结果的关键。儿科外科医生和临床医生必须对这种罕见的疾病保持高度的怀疑,以确保及时诊断并尽量减少相关的发病率和死亡率。
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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来源期刊
Case Reports in Gastroenterology
Case Reports in Gastroenterology Medicine-Gastroenterology
CiteScore
1.10
自引率
0.00%
发文量
99
审稿时长
7 weeks
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