Perforated meckel's diverticulum misdiagnosed as a urinary tract infection in an 11-year-old adolescent: case report of a rare differential diagnosis.

IF 2.6 Q1 SURGERY
Mohamed Ali, Hisham Hazem Warda, Ahmed Elghrieb
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Abstract

Background: Meckel's diverticulum, a congenital anomaly of the gastrointestinal tract, is often asymptomatic but can present with complications such as inflammation, perforation, or obstruction. Misdiagnosis is common owing to its varied presentations, particularly when symptoms mimic other conditions such as urinary tract infections (UTI).

Case presentation: An 11-year-old boy presented with persistent suprapubic pain and dysuria for one week. Initial urine analysis revealed turbid urine with high numbers of red blood cells, leading to a diagnosis of urinary tract infection (UTI), and antibiotic treatment was initiated. However, the patient's symptoms persisted, with worsening clinical signs. A complete blood count revealed leukocytosis with neutrophilia, suggesting the need for further evaluation. A non contrast computed tomography (CT) scan revealed a thickened, blind-ended structure in the midline lower abdomen with gas, extensive fat stranding, and associated mesenteric lymphadenopathy, suggestive of perforated Meckel's diverticulum. The patient underwent laparoscopic exploration, which revealed an abscess caused by perforated Meckel's diverticulum adherent to the urinary bladder. Diverticulectomy and incidental appendectomy were performed via a stapling device. Pathology confirmed a perforation of Meckel's diverticulum with serofibrinous peritonitis and follicular appendicitis. The postoperative course was uneventful, with the patient resuming full oral intake by the fifth day and being discharged in stable condition.

Conclusion: This case emphasizes how Meckel's diverticulum can mimic a urinary tract infection, especially in pediatric patients with overlapping symptoms like suprapubic pain and dysuria. The delayed diagnosis highlights the importance of reconsidering rare causes when symptoms persist. Timely imaging was crucial in guiding effective treatment.

11岁青少年穿孔梅克尔憩室误诊为尿路感染:罕见鉴别诊断病例报告。
背景:梅克尔憩室是一种先天性胃肠道异常,通常无症状,但可出现炎症、穿孔或梗阻等并发症。误诊是常见的,由于其不同的表现,特别是当症状模仿其他条件,如尿路感染(UTI)。病例介绍:一名11岁男孩表现为持续耻骨上疼痛和排尿困难一周。最初的尿液分析显示尿液浑浊,红细胞数量多,导致尿路感染(UTI)的诊断,并开始抗生素治疗。然而,患者的症状持续存在,临床体征恶化。全血细胞计数显示白细胞增多伴中性粒细胞增多,提示需要进一步检查。非对比CT扫描显示下腹部中线处增厚、盲端结构,伴气体、广泛脂肪搁浅及相关肠系膜淋巴结病变,提示梅克尔憩室穿孔。患者行腹腔镜探查,发现一脓肿,由附着于膀胱的梅克尔憩室穿孔引起。憩室切除术和意外阑尾切除术通过吻合器进行。病理证实梅克尔憩室穿孔伴浆液性腹膜炎和滤泡性阑尾炎。术后过程平稳,患者于第五天恢复完全口服,出院时病情稳定。结论:本病例强调了Meckel憩室如何模拟尿路感染,特别是在耻骨上疼痛和排尿困难等重叠症状的儿科患者中。延迟的诊断强调了当症状持续时重新考虑罕见病因的重要性。及时成像对指导有效治疗至关重要。
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
CiteScore
6.80
自引率
8.10%
发文量
37
审稿时长
9 weeks
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