Arredondo Montero Javier, Rico-Jiménez María
Pediatric Surgery Department, Complejo Asistencial Universitario de León, 24008 León, Castilla y León, Spain.
Pediatric Surgery Department, Hospital Universitario Niño Jesús, 28009 Madrid, Spain.
Children (Basel). 2025 Aug 25;12(9):1120. doi: 10.3390/children12091120.
Spigelian hernia (SH) is an infrequent aponeurotic defect in Spiegel's semilunar line. The literature on pediatric SH is scarce. A comprehensive review of the previous literature was conducted. Eligible studies were identified by searching primary medical bibliography databases, and a pooled analysis of published case-level data was performed. Medians and interquartile ranges were used to describe the quantitative variables and proportions for categorical variables. The Kruskal-Wallis, Mann-Whitney U, and Fisher's exact tests were used to compare group variables. Spearman's and Pearson's correlation analyses were used to assess the degree of correlation between variables, while Cramér's V was applied to evaluate the degree of association among the variables. A -value < 0.05 (two-tailed) was considered statistically significant. Our search identified 82 publications reporting on 123 patients (106 male, 86.2%), with an age range of 0-21 years. Forty-seven patients (38.2%) had a left-sided SH, fifty-six (45.5%) had a right-sided SH, and thirteen (10.6%) had a bilateral SH. Traumatic SH, mostly from bicycle injuries, accounted for 45 cases (36.6%), while 41 (33.3%) were associated with undescended testis (UDT). In this series of published cases, hernia incarceration/strangulation (I/S) was reported in 15 patients (12.2%), who were significantly younger ( = 0.02). Surgical correction was performed in 95 cases (77.2%), 14 of them laparoscopically, with a 35.7% conversion rate. Eight cases (6.5%) were managed conservatively. Overall, outcomes were favorable. SH is an infrequent pediatric condition that, based on the synthesized literature, predominantly affects males. The published cases suggest two main clinical phenotypes: a congenital form, often linked to ipsilateral UDT, and an acquired form, typically resulting from trauma. Analysis of the reported data indicates a higher risk of incarceration in early childhood. Surgical treatment is the most frequently reported approach with generally favorable outcomes, whereas the evidence for conservative management remains limited. This comprehensive review highlights the dual nature of pediatric SH and underscores the need for a high index of suspicion in relevant clinical scenarios.
半月线疝(SH)是半月线处一种罕见的腱膜缺损。关于小儿半月线疝的文献较少。我们对既往文献进行了全面综述。通过检索主要医学文献数据库确定符合条件的研究,并对已发表的病例级数据进行汇总分析。中位数和四分位数间距用于描述定量变量,分类变量则用比例表示。采用Kruskal-Wallis检验、Mann-Whitney U检验和Fisher精确检验比较组间变量。使用Spearman相关性分析和Pearson相关性分析评估变量之间的相关程度,同时应用Cramér's V评估变量之间的关联程度。P值<0.05(双侧)被认为具有统计学意义。我们的检索共识别出82篇报告123例患者的文献(106例男性,占86.2%),年龄范围为0至21岁。47例患者(38.2%)为左侧半月线疝,56例(45.5%)为右侧半月线疝,13例(10.6%)为双侧半月线疝。创伤性半月线疝大多由自行车损伤导致,共45例(36.6%),而41例(33.3%)与隐睾(UDT)相关。在这一系列已发表的病例中,15例患者(12.2%)报告有疝嵌顿/绞窄(I/S),这些患者明显更年幼(P = 0.02)。95例患者(77.2%)接受了手术矫正,其中14例采用腹腔镜手术,中转开腹率为35.7%。8例患者(6.5%)接受了保守治疗。总体而言,预后良好。半月线疝是一种罕见的小儿疾病,根据综合文献,主要影响男性。已发表的病例提示两种主要临床表型:一种是先天性形式,常与同侧隐睾相关;另一种是后天性形式,通常由创伤引起。对报告数据的分析表明幼儿期嵌顿风险较高。手术治疗是最常报道的治疗方法,总体预后良好,而保守治疗的证据仍然有限。这一全面综述突出了小儿半月线疝的双重性质,并强调在相关临床场景中需要高度怀疑。