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Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
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Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
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Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review

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Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review
Journal Article

Pediatric Spigelian Hernia and Spigelian–Cryptorchidism Syndrome: An Integrative Review

2025
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Overview
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 p-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 (p = 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.