Femoral hernias: A paediatric surgical enigma.


Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 04 03 2021
accepted: 12 03 2021
pubmed: 19 4 2021
medline: 29 6 2021
entrez: 18 4 2021
Statut: ppublish

Résumé

In the paediatric population, femoral hernia (FH) represents an uncommon and often misdiagnosed pathology. This study aimed to review our experience with the management of FH in children. Medical records were retrospectively reviewed for all patients presenting to the paediatric surgical service in Ireland over a 15-year period (2004-2019), who were operated on for FH. Collected data included demographics, preoperative diagnosis, operative details, complications and follow-up. During the study period, n = 26 patients (n = 18 males) underwent FH repair, with a median age at surgery 6.9 years (range 3-16 years). During the same period n = 5693 patients underwent inguinal herniotomy, resulting in a FH to inguinal hernia (IH) ratio of 1:219 and a FH incidence of 0.45% of all groin hernias. The right side was affected in n = 18 (69.2%) cases and all cases were unilateral. A correct preoperative diagnosis was established in n = 16 (61.5%) cases, n = 8 (30.8%) cases were misdiagnosed as IH and the diagnosis was equivocal in 2 cases (7.7%). All operations were performed on an elective basis. In 3 patients from the misdiagnosed group, FH was found at first operation following negative groin exploration for IH. The remaining 5 patients underwent previous groin exploration for suspected IH and represented with clinical picture of groin hernia recurrence. All patients with a correct preoperative diagnosis underwent a FH repair via an inguinal or infra-inguinal approach. The content of the hernia sac was preperitoneal fat in n = 18 cases, lymph nodes in n = 2 cases, omentum in n = 1 and an empty sac in n = 1. There were no postoperative complications or recurrences. Median follow-up time was 6 weeks (range 0-2.5 years). In the paediatric population, FH is a rare pathology and can be a challenging diagnosis. FH is commonly misdiagnosed as IH and may require more than one operation to correctly identify and treat. A high index of suspicion of FH should be maintained in patients who have a negative groin exploration for IH in the setting of a clear pre-operative diagnosis of a groin hernia. FH should also be considered in the differential diagnosis when an IH appears to recur.

Identifiants

pubmed: 33865603
pii: S0022-3468(21)00266-9
doi: 10.1016/j.jpedsurg.2021.03.032
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1132-1135

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflict of interest.

Auteurs

Ancuta Muntean (A)

Children's Health Ireland at Crumlin, Cooley Rd, Crumlin D12 N512, Dublin, Ireland. Electronic address: ancutza_muntean@yahoo.com.

Ionica Stoica (I)

Children's Health Ireland at Tallaght, Tallaght University Hospital, Tallaght D24 NR0A, Dublin, Ireland.

Danielle McLaughlin (D)

Children's Health Ireland at Temple Street, Temple Street, D01 XD99, Dublin, Ireland.

John Gillick (J)

Children's Health Ireland at Crumlin, Cooley Rd, Crumlin D12 N512, Dublin, Ireland; Children's Health Ireland at Temple Street, Temple Street, D01 XD99, Dublin, Ireland.

Farhan Khaliq Tareen (FK)

Children's Health Ireland at Crumlin, Cooley Rd, Crumlin D12 N512, Dublin, Ireland; Children's Health Ireland at Tallaght, Tallaght University Hospital, Tallaght D24 NR0A, Dublin, Ireland.

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Classifications MeSH