Skip to main content

CASE REPORT article

Front. Surg., 06 November 2024
Sec. Pediatric Urology

Ureteroinguinal hernia: an added advantage for laparoscopy in the management of inguinal hernia—a case report

\r\nMostafa ZainMostafa ZainOssama KasemOssama KasemMohamed GamalMohamed GamalAhmed Tayel
Ahmed Tayel*Mohamed Abouheba\r\nMohamed Abouheba
  • Department of Pediatric Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt

Different abdominal organs can herniate into the inguinal canal, including the small bowel, colon, appendix, ovaries, and, less commonly, the urinary bladder and fallopian tubes. Herniation of the ureter within an inguinal hernia is a very rare occurrence. To the best of our knowledge, less than 150 cases have been reported in the literature, including only 15 pediatric cases. A 3-month-old boy presented to our clinic with a left inguinal swelling. Ultrasound of the abdomen and pelvis showed grade 4 left hydronephrosis with a dilated tortuous ureter passing through the left inguinal canal. Further investigation revealed that the patient had a left primary obstructing megaureter with a ureteroinguinal hernia. The case was managed with laparoscopic repair of the inguinal hernia and urethrostomy. The current case proves an additional advantage for laparoscopy as it allows proper visualization of the anatomy and identification of atypical hernias, such as ureteroinguinal hernia.

Background

Inguinal hernia remains the most common surgical problem encountered by pediatric surgeons. The incidence of inguinal hernia in children ranges from 0.8%to 4.4% (1). It represents more than 15% of the workload in contemporary pediatric surgical practice and is generally considered a well-tolerated procedure with a low risk of significant complications (2). Different abdominal organs can herniate into the inguinal canal, including the small bowel, colon, appendix, ovaries, and, less commonly, the urinary bladder and fallopian tubes. Herniation of the ureter within an inguinal hernia is a very rare occurrence. To the best of our knowledge, less than 150 cases have been reported in the literature, including only 15 pediatric cases (36).

Since the 1990s, laparoscopic repair of inguinal hernia has gained popularity and has become the standard of care in many centers; however, the traditional open surgical approach is still the most commonly used technique worldwide (7). The use of laparoscopy offers many benefits, such as better cosmetic results, less postoperative pain, faster recovery, shorter hospital stays, and visualization of the contralateral deep inguinal ring. However, due to its increased cost, prolonged learning curve, and longer operative time, it has not achieved the global acceptance seen with other procedures, such as appendectomy and cholecystectomy (7). In this report, we describe the laparoscopic treatment of a ureteroinguinal hernia in a 3-month-old infant, which can be considered another advantage of using laparoscopy for inguinal hernia repair. This manuscript was prepared following the CARE guidelines (https://www.care-statement.org).

Case presentation

Our patient was a 3-month-old boy who was brought to our clinic by his mother who complained that her child had inguinal swelling on the left side. The mother said that she had noticed this swelling for 2 days. The boy was delivered by cesarean section at full term with a birth weight of 3.2 kg. Antenatal ultrasound (US) examinations were unremarkable. The patient's medical, surgical, and family histories were unremarkable. On clinical examination, the boy looked healthy with an irreducible left inguinal swelling. However, there were no signs or symptoms of intestinal obstruction. The provisional diagnosis was thought to be an irreducible left inguinal hernia. US of the abdomen and pelvis revealed a grade 4 hydronephrosis on the left side with a dilated tortuous ureter passing through the left inguinal canal. For better anatomic visualization, magnetic resonance urography (MRU) was carried out. It showed the enlarged left kidney in a normal position, with marked hydroureteronephrosis, dilated scattered calyces, and multiple kinks in the ureter. The dilated ureter extended into a moderately sized, fat-containing inguinal hernia (Figure 1).

Figure 1
www.frontiersin.org

Figure 1. Preoperative magnetic resonance urography showing left severe hydroureteronephrosis with dilated scattered calyces and multiple kinks in the ureter. The dilated ureter extends into a moderately sized, fat-containing inguinal hernia.

To determine whether the ureteric dilatation was due to obstruction or reflux, we performed a voiding cystourethrogram (VCUG), which showed normal bladder filling and voiding without any reflux. Therefore, the diagnosis of left primary obstructing megaureter with ureteroinguinal hernia was made. An isotopic dimercaptosuccinic acid (DMSA) renal scan showed normal homogeneous radioactive uptake in the right kidney, while the left kidney was enlarged in size showing moderate radioactive accumulation. There was no evidence of infection or scarring on either side. The relative uptake was 74% for the right kidney and 26% for the left kidney. The treatment plan included diagnostic cystoscopy, laparoscopic repair of the inguinal hernia, and urethrostomy.

The basic preoperative evaluation, including routine laboratory investigations and cardiac and anesthesia reviews. was normal. Diagnostic cystoscopy showed that the right ureteric orifice was normal and orthotopic, while the left ureteric orifice could not be visualized. After inserting a 5 mm umbilical trocar and introducing a 30° endoscope through the umbilicus, two 3-mm instruments were inserted directly (without trocars) at the right and left mid-clavicular lines, aligned at the level of the umbilicus, to maintain a triangular orientation. Laparoscopic exploration revealed a massively dilated and tortuous left ureter forming a loop sliding into the left inguinal canal with a small hernial sac (Figure 2).

Figure 2
www.frontiersin.org

Figure 2. Intraoperative laparoscopic photograph showing a massively dilated and tortuous left ureter (yellow arrow) forming a loop sliding into the left inguinal canal with a small hernial sac (blue dashed circle).

After disconnection of the hernial sac from the abdominal peritoneum, the ureter was reduced, and the internal inguinal ring was tightened with a single 4/0 prolene suture. The ureter was dissected down to its entrance into the urinary bladder, where it was separated. It was then exteriorized through a small incision in the left iliac region (Figure 3). A ureterostomy was performed after the excision of the excess dilated ureter. The postoperative course was uneventful. The boy resumed oral feeding on the first postoperative day and was discharged on the second day. The plan was to perform extravesical ureteric reimplantation when he reached the age of 1 year.

Figure 3
www.frontiersin.org

Figure 3. Intraoperative photograph after exteriorization of the ureter through a small incision in the left iliac region.

Discussion

Inguinal hernia is one of the most common surgical problems in children (8). It is estimated that more than 20 million hernia repairs are performed every year worldwide (9). The major complication of inguinal hernia, if left untreated, is incarceration, which can lead to intestinal gangrene and gonadal atrophy (10). The risk of incarceration in children ranges from 3% to–16% in different studies; however, in premature infants, it is estimated to be as high as 30% (11).

The usual contents of the inguinal hernia include the small intestine, colon, omentum, and ovaries. Less commonly, the appendix (Amyand's hernia) or Meckel's diverticulum (Littre hernia) may be present. In addition, the urinary bladder may herniate into a direct sac or form part of the wall in a sliding hernia (12). These uncommon findings pose a technical challenge, increasing the risk of inadvertent injury to these organs.

Herniation of the ureter into the inguinal canal is a very rare finding (4, 13). It was first reported in 1880 by Leroux as an autopsy finding (14). In 1892, Reichel reported the first case of ureteral hernia discovered during hernia repair (15). In 1937, Dourmashkin made the first preoperative diagnosis of a ureteral hernia using intravenous pyelography (16). A recent review of the literature by Laurie revealed that less than 150 cases were reported in the English literature (3). Cianci et al. reviewed pediatric cases and found 12 cases in addition to their own case (4). Later, two more pediatric cases were reported by Delgado-Miguel et al. and Wishahi (5, 7).

Ureteroinguinal hernia is classified based on the presence or absence of a hernial sac, classifying it as paraperitoneal or extraperitoneal, respectively (17). The extraperitoneal type is less common, accounting for only 20% of cases. The ureter develops from an outgrowth (ureteric bud) that originates from the mesonephric duct and also gives rise to the epididymis, vas deferens, seminal vesicles, and the ejaculatory duct. The extraperitoneal type results from an embryological abnormality in which the ureteric bud separates late from the Wolffian duct as it descends to form the epididymis. The ureter, with a significant amount of retroperitoneal fat, herniates into the inguinal canal in the absence of a hernial sac (18, 19).

On the other hand, the paraperitoneal type accounts for 80% of cases. It can be considered a sliding hernia, as the ureter, being a retroperitoneal structure, is part of the wall of the hernia sac rather than an internal component of the hernia. This type is more commonly associated with a dilated ureter, as seen in cases of vesicoureteral reflux, posterior urethral valve, and obstructing megaureter. It has been suggested that this type may develop due to traction on the ureter caused by abnormally adherent posterior parietal peritoneum (1820). This was the case with our patient.

Risk factors for ureteroinguinal hernia in adults include obesity, anterior displacement of the ureter from the psoas muscle, scarring from previous hernia repair, and renal transplantation (12). However, the risk factors in the pediatric population are still uncertain. In their review, Cianci et al. suggested congenital pathogenesis in children, noting that the majority of cases had an almost constant association with other congenital anomalies of the urogenital system. They stated that it is difficult to determine whether the dilated ureter found in the majority of cases results from the ureteroinguinal hernia or whether it serves as a predisposing factor, causing ureteric displacement toward the inguinal canal due to its convoluted course (4). In this context, our case involved a left primary obstructing megaureter with a massively dilated tortuous ureter, which may have contributed to the ureteric herniation into the inguinal canal.

Preoperative diagnosis of ureteric herniation is essential for appropriate surgical decisions and to minimize the risk of ureteric injury during operation; however, the majority of cases are identified intraoperatively (18). In the 15 reported pediatric cases, the ureteric injury occurred in 4 out of 7 cases without preoperative diagnosis during inguinal herniotomy, whereas in the other 8 cases with a preoperative diagnosis, no other operative complications were reported.

Ureteroinguinal hernia may be suspected in the presence of urinary symptoms such as dysuria, urinary frequency, or flank pain; however, most patients are asymptomatic (17). The routine preoperative workup for inguinal hernia does not require any specific imaging, as it is considered a straightforward clinical diagnosis and unusual findings are rare. Some authors advise increasing the index of suspicion for a ureteroinguinal hernia when an inguinal hernia presents in a patient with unexplained hydronephrosis or recurrent urinary tract infections, especially in male patients. In addition, if the traction of the testis on clinical examination of the external genitalia is associated with the appearance of an ipsilateral bulge, further evaluation may be warranted. In such cases, an algorithm proposed by Yahya et al. for adult patients suggests considering additional urological evaluation, including US, VCUG, and renal scintigraphy, while cystoscopy remains optional (12). A computed tomography (CT) scan or MRU may be considered in the pediatric population if US does not lead to a preoperative diagnosis (17). In our case, the diagnosis was suspected by US and confirmed by MRU.

During open surgery for an inguinal hernia, the possible presence of the ureter should be suspected if unusual structures are encountered in the operative field, especially if they are found outside the hernial sac. Consideration should be given to the probability of herniating retroperitoneal structures, especially the ureter if the hernia contains fat that does not fit the criteria of a cord lipoma. In such cases, cautious fat reduction should be carried out. If complete reduction of the fat is not possible, careful dissection to the level of the deep ring is necessary to prevent ureteric damage (12, 20). In this context, the laparoscopic approach is ideal, as it allows for a thorough inspection of the inguinal and pelvic regions (4).

Failure to achieve a preoperative diagnosis and recognize ureteric involvement intraoperatively may result in high morbidity and even mortality. The ureter, buried beneath a thick layer of fat, may be mistaken for extraperitoneal fat or a cord lipoma, resulting in injury from blind clamping and division (21). Given the number of hernia surgeries performed worldwide, routine CT scans, or MRU, are not justified; however, they are recommended for patients with abnormal renal function tests or urinary symptoms. Therefore, the laparoscopic approach offers a great advantage by providing proper visualization of the anatomy before division (21).

Laparoscopic repair of inguinal hernias has gained popularity worldwide over the past three decades; however, it is still less common than the open approach due to its high cost, longer operative time, conversion from an extraperitoneal procedure to an intraperitoneal one, and longer learning curve (22, 23). However, laparoscopy offers many advantages over the open approach, such as detection and repair of contralateral hernias during the same session, magnification, reduced manipulation of the vas deferens and testicular vessels in male patients, less postoperative pain, and a better cosmetic outcome. It is also considered to be the best option for managing recurrent inguinal hernias (22, 24). In addition, it allows for the identification of atypical hernias, such as ureteroinguinal hernias, even in cases without preoperative diagnosis (4, 21).

The management of ureteroinguinal hernias in adults is debatable as the majority of authors recommend hernia repair with retroperitoneal relocation of the ureter, while others propose conservative management (25). On the contrary, surgical repair is essential for pediatric ureteroinguinal hernias, as they are usually paraperitoneal and involve a hernial sac that requires independent repair from the associated ureteral herniation. In addition, it is difficult to discriminate between the paraperitoneal and extraperitoneal types preoperatively (4).

If there is no associated megaureter or other anomalies, the patient will require only hernial repair with the relocation of the ureter to the retroperitoneum (25, 26). Alternatively, in cases involving a severely dilated ureter, management will depend on the primary pathology. Various procedures have been described in the reported pediatric cases, including partial resection, ureterostomy, ureteric reimplantation, and transureteroureterostomy (2730). In our patient, we performed a temporary ureterostomy and planned for future ureteric reimplantation as a result of the patient’s young age and the significant degree of ureteric dilatation. Reimplantation of a grossly dilated ureter into a small infant urinary bladder could be a challenging operation in young infants, as the discrepancy between the dilated ureter and the small bladder raises concerns about potential iatrogenic bladder dysfunction (31, 32). For infants under 1 year of age with a primary obstructing megaureter that requires intervention, the British Association of Paediatric Urologists’ consensus statement supports temporizing measures such as stenting, balloon dilatation, temporary refluxing reimplantation, or cutaneous ureterostomy. It recommends delaying definitive reimplantation surgery until the child is 1 year old (33).

Conclusion and recommendations

The current case demonstrates the importance of preoperative evaluation and diagnosis of ureteroinguinal hernia. It also emphasizes how this rare condition may go unnoticed during the standard preoperative evaluation for elective day-case inguinal hernia repair. We recommend performing an US evaluation in cases of irreducible inguinal hernia that do not present with signs of intestinal obstruction.

It also highlights an additional advantage of laparoscopy, as it allows for proper visualization of the anatomy and identification of atypical hernias, such as ureteroinguinal hernias, even in cases without a preoperative diagnosis, as well as the other reported advantages of the laparoscopic approach.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving humans were approved by the Ethical Committee of the Alexandria Faculty of Medicine. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin. Written informed consent was obtained from the minor(s)' legal guardian/next of kin for the publication of any potentially identifiable images or data included in this article.

Author contributions

MZ: Writing – original draft. OK: Data curation, Investigation, Writing – original draft. MG: Data curation, Writing – original draft. AT: Investigation, Methodology, Writing – original draft. MA: Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

MRU, magnetic resonance urography; US, ultrasound; VCUG, voiding cystourethrogram.

References

1. Morini F, Dreuning KMA, Janssen Lok MJH, Wester T, Derikx JPM, Friedmacher F, et al. Surgical management of pediatric inguinal hernia: a systematic review and guideline from the European pediatric Surgeons’ association evidence and guideline committee. Eur J Pediatr Surg. (2022) 32(3):219–32. doi: 10.1055/s-0040-1721420

PubMed Abstract | Crossref Full Text | Google Scholar

2. Ein SH, Njere I, Ein A. Six thousand three hundred sixty-one pediatric inguinal hernias: a 35-year review. J Pediatr Surg. (2006) 41(5):980–6. doi: 10.1016/j.jpedsurg.2006.01.020

PubMed Abstract | Crossref Full Text | Google Scholar

3. Laurie BD. Unexpected ureter within an inguinal hernia. Cureus. (2023) 15(3):e36691. doi: 10.7759/cureus.36691

PubMed Abstract | Crossref Full Text | Google Scholar

4. Cianci MC, Tocchioni F, Mantovani A, Ghionzoli M, Morini F. Unexpected pediatric uretero-inguinal hernia: case-report and literature review. Urology. (2023) 176:178–82. doi: 10.1016/j.urology.2023.02.015

PubMed Abstract | Crossref Full Text | Google Scholar

5. Delgado-Miguel C, Muñoz-Serrano AJ, Aguado P, Fuentes E, Díez R. Ureteroinguinal herniation with consecutive ureteral stricture in a 2-month-old infant: case report. European J Pediatr Surg Rep. (2024) 12(01):e16–9. doi: 10.1055/s-0044-1779253

PubMed Abstract | Crossref Full Text | Google Scholar

6. Goneidy A, Verhoef C, Lansdale N, Peters RT, Wilkinson DJ. Laparoscopic hernia repair in children: does recreating the open operation improve outcomes? A systematic review. Hernia. (2023) 27(5):1037–46. doi: 10.1007/s10029-023-02772-5

PubMed Abstract | Crossref Full Text | Google Scholar

7. Wishahi M. Congenital primary obstructed megaureter presenting as inguinal hernia in an infant. Clin Case Rep. (2022) 10(4):e05677. doi: 10.1002/ccr3.5677

PubMed Abstract | Crossref Full Text | Google Scholar

8. Lao OB, Fitzgibbons RJ Jr, Cusick RA. Pediatric inguinal hernias, hydroceles, and undescended testicles. Surg Clin North Am. (2012) 92(3):487–504. doi: 10.1016/j.suc.2012.03.017

PubMed Abstract | Crossref Full Text | Google Scholar

9. Puri P, Guiney EJ, O’Donnell B. Inguinal hernia in infants: the fate of the testis following incarceration. J Pediatr Surg. (1984) 19(1):44–6. doi: 10.1016/S0022-3468(84)80013-5

PubMed Abstract | Crossref Full Text | Google Scholar

10. van Heurn LW, Pakarinen MP, Wester T. Contemporary management of abdominal surgical emergencies in infants and children. Br J Surg. (2014) 101(1):e24–33. doi: 10.1002/bjs.9335

PubMed Abstract | Crossref Full Text | Google Scholar

11. Rescorla FJ, Grosfeld JL. Inguinal hernia repair in the perinatal period and early infancy: clinical considerations. J Pediatr Surg. (1984) 19(6):832–7. doi: 10.1016/S0022-3468(84)80379-6

PubMed Abstract | Crossref Full Text | Google Scholar

12. Yahya Z, Al-Habbal Y, Hassen S. Ureteral inguinal hernia: an uncommon trap for general surgeons. Case Reports. (2017) 2017:bcr2017219288.

Google Scholar

13. Pirvu C, Pantea S, Popescu A, Grigoras ML, Bratosin F, Valceanu A, et al. Difficulties in diagnosing extraperitoneal ureteroinguinal hernias: a review of the literature and clinical experience of a rare encounter in acute surgical care settings. Diagnostics. (2022) 12(2):353. doi: 10.3390/diagnostics12020353

PubMed Abstract | Crossref Full Text | Google Scholar

14. Carli C. L’ernia dell’uretere. Ann Ital Chir. (1932) 11:2078–104.

Google Scholar

15. Reichel P. Ueber hernienart vorfall eines ureters durch den leisten kanal. Arch Klin Chir. (1892) 44:430–7.

Google Scholar

16. Dourmashkin RL. Scrotal hernia of ureter, associated with a unilateral fused kidney: a case report. J Urol. (1937) 38(5):455–67. doi: 10.1016/S0022-5347(17)71975-1

Crossref Full Text | Google Scholar

17. McKay JP, Organ M, Bagnell S, Gallant C, French C. Inguinoscrotal hernias involving urologic organs: a case series. Can Urol Assoc J. (2014) 8(5-6):429. doi: 10.5489/cuaj.225

PubMed Abstract | Crossref Full Text | Google Scholar

18. Turner A, Subramanian P. Ureteroinguinal hernia: a rare general surgery phenomenon. Cureus. (2021) 13:12. doi: 10.7759/cureus.20586

PubMed Abstract | Crossref Full Text | Google Scholar

19. Sidiqi MM, Menezes G. Asymptomatic herniation of ureter in the routine inguinal hernia: a dangerous trap for general surgeons. Int J Surg Case Rep. (2018) 49:244–6. doi: 10.1016/j.ijscr.2018.07.013

PubMed Abstract | Crossref Full Text | Google Scholar

20. Eilber KS, Freedland SJ, Rajfer J. Obstructive uropathy secondary to ureteroinguinal herniation. Rev Urol. (2001) 3(4):207.16985719

PubMed Abstract | Google Scholar

21. Narayanan PL, Narayanan CD, Sekar V, Vadyala AR. Laparoscopic approach to ureteroinguinal hernia. Int J Surg Case Rep. (2020) 77:161–4. doi: 10.1016/j.ijscr.2020.10.127

PubMed Abstract | Crossref Full Text | Google Scholar

22. Davies DA, Rideout DA, Clarke SA. The international pediatric endosurgery group evidence-based guideline on minimal access approaches to the operative management of inguinal hernia in children. J Laparoendosc Adv Surg Tech. (2020) 30(2):221–7. doi: 10.1089/lap.2016.0453

PubMed Abstract | Crossref Full Text | Google Scholar

23. Schmedding A, Alsweed A, Muensterer O, Leonhardt J. The status of laparoscopic inguinal hernia surgery in children: a nationwide assessment. Children. (2022) 9(3):348. doi: 10.3390/children9030348

PubMed Abstract | Crossref Full Text | Google Scholar

24. Bada-Bosch I, Escolino M, De Agustín JC, Esposito C. Pediatric inguinal hernia repair, laparoscopic versus open approach: a systematic review and meta-analysis of the last 10-year evidence. J Laparoendosc Adv Surg Tech. (2022) 32(5):583–94. doi: 10.1089/lap.2021.0690

PubMed Abstract | Crossref Full Text | Google Scholar

25. Burgu B, Reşorlu B, Süer E, Soygür T. Scrotal hernia of the ureter in association with posterior urethral valves. J Pediatr Urol. (2010) 6(1):87–8. doi: 10.1016/j.jpurol.2009.05.008

PubMed Abstract | Crossref Full Text | Google Scholar

26. Giglio M, Medica M, Germinale F, Raggio M, Campodonico F, Stubinski R, et al. Scrotal extraperitoneal hernia of the ureter: case report and literature review. Urol Int. (2001) 66(3):166–8. doi: 10.1159/000056601

PubMed Abstract | Crossref Full Text | Google Scholar

27. Cao K, Turner M, Mishrah P, Cuckow P. The rare case of an extraperitoneal ureteral herniation into the inguinal canal of a 12-year-old boy. Ann R Coll Surg Engl. (2019) 101:e32–4. doi: 10.1308/rcsann.2018.0176

PubMed Abstract | Crossref Full Text | Google Scholar

28. Powell MC, Kapila L. Bilateral megaureters presenting as an inguinal hernia. J Pediatr Surg. (1985) 20:175–6. doi: 10.1016/S0022-3468(85)80296-7

PubMed Abstract | Crossref Full Text | Google Scholar

29. Bosschieter J, van Roij K, Ahmadi N, Bokenkamp A, van der Horst HJR. Kidney blow out due to inguinal herniation of the ureter in an infant. Urol Int. (2018) 100:488–90. doi: 10.1159/000449015

PubMed Abstract | Crossref Full Text | Google Scholar

30. Handu AT, Garge S, Peters NJ, Kanojia RP, Rao KL. Undiagnosed ureteroinguinal hernia with solitary kidney in a child with ureteric injury during herniotomy. J Pediatr Surg. (2012) 47:799–802. doi: 10.1016/j.jpedsurg.2012.01.006

PubMed Abstract | Crossref Full Text | Google Scholar

31. Tröbs RB, Heinecke K, Elouahidi T, Nounla J, Kluge R. Renal function and urine drainage after conservative or operative treatment of primary (obstructive) megaureter in infants and children. Int Urol Nephrol. (2006) 38:141–7. doi: 10.1007/s11255-005-3615-5

PubMed Abstract | Crossref Full Text | Google Scholar

32. de Kort LM, Klijn AJ, Uiterwaal CS, de Jong TP. Ureteral reimplantation in infants and children: effect on bladder function. J Urol. (2002) 167(1):285–7. doi: 10.1016/S0022-5347(05)65451-1

PubMed Abstract | Crossref Full Text | Google Scholar

33. Farrugia MK, Hitchcock R, Radford A, Burki T, Robb A, Murphy F. British Association of Paediatric Urologists consensus statement on the management of the primary obstructive megaureter. J Pediatr Urol. (2014) 10(1):26–33. doi: 10.1016/j.jpurol.2013.09.018

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: ureteroinguinal hernia, laparoscopy, hernia (inguinal), hydroureter, extraperitoneal hernia

Citation: Zain M, Kasem O, Gamal M, Tayel A and Abouheba M (2024) Ureteroinguinal hernia: an added advantage for laparoscopy in the management of inguinal hernia—a case report. Front. Surg. 11:1415875. doi: 10.3389/fsurg.2024.1415875

Received: 11 April 2024; Accepted: 7 October 2024;
Published: 6 November 2024.

Edited by:

Lisandro Ariel Piaggio, Universidad Nacional del Sur, Argentina

Reviewed by:

Carlos Delgado-Miguel, Hospital Infantil La Paz, Spain
Miguel Alfedo Castellan, University of Miami, United States
Alexandros Chamzin, National and Kapodistrian University of Athens, Greece

Copyright: © 2024 Zain, Kasem, Gamal, Tayel and Abouheba. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ahmed Tayel, YWhtZWRhYmRlbGxhdGVmYW1pbkBnbWFpbC5jb20=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.