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. 2020 Apr 1;13(4):600–604. doi: 10.1111/ases.12800

Primary anterior perineal hernia: A case report and review of the literature

Ikuo Watanobe 1,, Shozo Miyano 1, Michio Machida 1, Hiroyuki Sugo 1
PMCID: PMC7687169  PMID: 32239652

Abstract

Perineal hernia is a type of pelvic floor hernia and an extremely rare pathologic state. Perineal hernias can be classified into anterior and posterior types according to their positional relationship to the superficial transverse perineal muscle. A 49‐year‐old woman presented with bulging of the right labium major while standing. Standing external ultrasonography revealed a mass in the bulge, which could not be identified by transvaginal ultrasonography, CT, or MRI. Although hernia content could not be identified preoperatively, the patient was given a diagnosis of primary perineal hernia and underwent laparoscopic repair. Symptoms resolved postoperatively, and no sign of relapse has been noted for 8 months postoperatively. Here, we report the case details and review previous case reports.

Keywords: laparoscopic repair, primary anterior perineal hernia, primary perineal hernia

1. INTRODUCTION

Pelvic floor hernia is extremely rare, particularly obturator, perineal, and sciatic hernias.1 Primary perineal hernias occur most commonly in individuals aged 40 to 60 years and are five times more common in women than in men.1 Controversy remains regarding treatment, with various surgical approaches and hernia repair techniques reported in the literature. This appears to be due to varying sites and sizes of hernial orifices and the anatomical complexity of the pelvic floor. Therefore, it currently appears to be necessary to individualize treatment strategies for each case.

2. CASE PRESENTATION

For 5 months before presentation, a 49‐year‐old woman (BMI, 18.7 kg/m2) noticed pudendal discomfort and swelling that occurred after prolonged standing. She consulted our hospital because the discomfort had recently progressed to pain while standing. On presentation, a thumb tip‐sized mass was seen in the right labium major on standing and disappeared on lying down. There was no tenderness, but she had mild pain at the site when increased intra‐abdominal pressure occurred such as during defecation. She had never been pregnant. Her medical history included an 8‐cm uterine myoma diagnosed at age 45 years for which she was being observed.

When the patient was in a standing position, bulging of the right labium major was noted with a palpable mass (Figure 1). Standing external ultrasonography revealed a 3‐cm oval, partially hypoechoic mass. Serial ultrasonography showed no intestinal peristalsis. Transvaginal ultrasonography revealed no corresponding mass in the pelvic floor region. CT and MRI showed no findings suggestive of a hernia, atrophy, a pelvic floor musculature defect, or a mass shadow in the perineal region. Barium enema showed no intestine reaching the pelvic floor, and no intestinal prolapse was observed on images taken with the patient in the standing position with abdominal pressure (Figure 2).

Figure 1.

Figure 1

Perineal region of the patient in the standing position. A bulging mass (arrow) noted in the right labium major in the standing position. A mobile, relatively soft mass was palpable directly under the skin

Figure 2.

Figure 2

Barium enema image (taken while the patient was standing). The mass observed in the perineal region is indicated by the tip of the forceps. The possibility of the hernia content being rectum or colon was excluded

Although the hernia content could not be identified, the mass was diagnosed as a primary acquired anterior perineal hernia, and laparoscopic repair was performed. A 2‐cm hernial orifice was found in the pouch of Douglas; the lumen extended toward the perineal region as confirmed by insertion of forceps into the orifice (Figure 3). The hernial orifice was closed by using nonabsorbable sutures, with additional closure of the uterosacral ligament with nonabsorbable sutures. The patient was discharged from the hospital 3 days postoperatively and has been symptom‐free for 8 months as of this writing.

Figure 3.

Figure 3

Hernial orifice found intraoperatively. A 2‐cm hernial orifice was found in the pouch of Douglas; the lumen extended up to the perineal region

3. DISCUSSION

Pelvic floor hernia is rare, and perineal hernia is an extremely rare pathologic state that surgeons might encounter once in their career,2 if ever. Stamatiou et al reported that Garangeot was the first to publish a case of primary perineal hernia in 1743.3 To our knowledge, Thomas first classified vaginal hernias into five groups in 1885.4 Furthermore, in 1940, Wilensky and Kaufman classified pelvic floor hernias as extravaginal, peritoneal vaginal, perineal, hedrocele, pudendal, and pelvic quasi hernias.5

Perineal hernia mainly occurs secondary. Many secondary perineal hernias occur after perineal gland operation within 1 year of the antecedent surgery.

Anterior perineal hernia occurs in the triangle‐shaped urogenital diaphragm surrounded by the ischiocavernosus, bulbocavernosus, and superficial transverse perineal muscles, and it affects only women.2 Because the anterior hernia is located in the urogenital diaphragm, the typical clinical symptom is prolapse around the labia. Critical cases advance to incontinence. For posterior perineal hernia, the typical symptom is a unilateral bulging in the gluteal or perineal region. In the present case, the patient had bulging of the labium major and was diagnosed with primary acquired anterior perineal hernia.

Clinical diagnosis of perineal hernia can be made using sonography, CT, MRI, and herniography6; an upright position during examination enables identification and anatomic association of the protruded bowel segment. Sometimes, perineal hernia may be mistaken for lipoma, fibroma, Bartholin cyst, rectocele, cystocele, or rectal prolapse. In our case, imaging showed no atrophy or pelvic floor muscular defect, and local external ultrasonography could visualize but not identify the hernia content.

Various approaches using mesh for closure of the pelvic defect have been reported for perineal hernia surgical repair, but the ideal approach has yet to be established. Sorelli et al recently reported THE advantages of the laparoscopic approach in perineal hernia repair.7 Ghellai et al and Franklin et al reported a laparoscopic approach using such mesh for pelvic defect closure.8, 9 For repair, direct suturing is considered an effective option, but it should be used with care because of its associations with relapse.10 Cali et al reported a recurrence‐free case using nonabsorbable mesh repair for a large pelvic floor defect.1 Simple approximation of the defect may be feasible in some cases, but in long‐standing cases, the pelvic floor is deficient and requires autologous or prosthetic materials. In our case, we chose laparoscopic surgery. We identified a hernial sac extending up to the labium from the pouch of Douglas. Because the hernial orifice was small and the patient was young and could possibly undergo surgery for uterine myoma or other pelvic surgery in the future, we opted to use a double suture closure method consisting of direct suturing plus uterosacral ligament suturing, instead of mesh. No sign of relapse has been noted for 8 months postoperatively.

Table 1 summarizes 29 retrievable case reports of primary perineal hernia with detailed descriptions, including our case. There were 4 congenital and 25 acquired cases. All six cases of anterior perineal hernia were in women; our case is the latest report of the anterior type. There were 23 cases of posterior perineal hernia. All the congenital cases were of posterior type. Most cases initially manifested with bulging. Hernia content comprised intestine in most cases. Prolapse of the urinary bladder or greater omentum was noted in rare cases. Surgical approaches included transabdominal in 13 cases, transperineal in 2 cases, abdominoperineal in 2 cases, and laparoscopic in 5 cases; an additional two cases were managed by follow‐up observation without surgery. Hernia relapse was reported in one case of anterior perineal hernia treated via a transabdominal approach using suture closure.10 The relapse occurred 18 months postoperatively and was treated with repeat surgery via a perineal approach. Mesh was used in 10 cases and placed via an abdominal approach in most cases, except for one case in which a perineal approach was used.

Table 1.

Reported perineal hernia (n = 29)

Author Reported year Age (y) Gender Congenital or acquired Position Symptom Hernia content Surgical approach Procedure
Case 1 Kondo 1936 26 Female Ac P Bulging Bowel Abdominal Suture
Case 2 Hirata 1947 40 Female Ac P Bulging Bowel None Conservative
Case 3 Amos 1951 40 Female Ac P Bulging Small bowel Abdominal Suture
Case 4 Richard and Ruben 1968 53 Male Ac P Bulging Sigmoid colon Abdominal Suture
Case 5 Thomford and Sherman 1969 66 Male Ac P Rectal pain Small bowel None Conservative
Case 6 Coussement et al 1978 0 (day 0) Female C P Bulging Rectum N/A N/A
Case 7 Coussement et al 1978 0 (day 2) N/A C P Bulging N/A N/A N/A
Case 8 Sato et al 1979 44 Female Ac A Bulging + pain N/A Abdominal Suture (recurrence)
Case 9 Vincent et al 1984 70 Female Ac P Painful mass Rectum Abdominal Suture + muscle flap
Case 10 Hubbard and Egelhoff 1989 0 (day 1) Female C P Bulging Colon N/A N/A
Case 11 Edward et al 1990 68 Male Ac P Bulging Sigmoid colon + small bowel N/A N/A
Case 12 Rebecca et al 1992 64 Female Ac P Constipation Sigmoid colon Abdominal Mesh
Case 13 Ito et al 1994 67 Female Ac P Bulging N/A Abdominal Suture + broad ligament of uterus patch
Case 14 Padilla et al 1999 35 Female Ac A Bulging N/A Perineal Mesh
Case 15 Yagi et al 2000 47 Female Ac A Bulging N/A Laparoscopy Mesh
Case 16 Kuroki 2001 72 Female Ac A Bulging N/A Abdominal Suture + mesh
Case 17 Amano 2002 68 Female Ac P Discomfort Sigmoid colon Abdominal Suture
Case 18 Mara et al 2005 68 Female Ac P Discomfort Sigmoid colon Abdominoperineal Mesh
Case 19 Preiss et al 2006 75 Female Ac P Back pain Small bowel + omentum Abdominal Suture
Case 20 Dirk et al 2006 67 Female Ac P Protrusion Small bowel Abdominal Suture + mesh
Case 21 Jessica et al 2009 57 Female Ac P Fullness+ pain Small bowel Laparoscopy Suture
Case 22 Washiro et al 2010 81 Female Ac P Discomfort Small bowel Abdominal Uterus patch
Case 23 Sorelli et al 2011 45 Female Ac A Discomfort N/A Laparoscopy Mesh
Case 24 Dragan et al 2012 0 (day 0) Female C P Bulging Rectum Perineal Suture
Case 25 Raghunath and Rajgopal 2013 42 Female Ac P Bulging Small bowel + colon + urinary bladder Abdominoperineal Suture + mesh
Case 26 Kurumboor and Palanisami 2013 63 Female Ac P Bulging Urinary bladder Laparoscopy Mesh
Case 27 Jorge and Juan 2017 71 Male Ac P Bulging Sigmoid colon + rectum Abdominal Mesh
Case 28 Mistry et al 2018 87 Female Ac P None (incidental) Small bowel + omentum N/A N/A
Case 29 Our case 49 Female Ac A Bulging Unknown Laparoscopy Suture

Abbreviations: A, anterior; Ac, acquired; C, congenital; N/A, not available; P, posterior.

We reported this very rare case of primary acquired anterior perineal hernia as we believe it was a valuable clinical experience worth sharing.

DISCLOSURE OF INTERESTS

The authors have no conflicts of interest to disclose and received no funding for this report.

ETHICS STATEMENT

This study received institutional review board approval, and it conforms to the provisions of the Declaration of Helsinki. The subject gave informed consent, and patient anonymity was preserved.

Supporting information

Watanobe I, Miyano S, Machida M, Sugo H. Primary anterior perineal hernia: A case report and review of the literature. Asian J Endosc Surg. 2020;13:600–604. 10.1111/ases.12800

REFERENCES

  • 1. Cali RL, Pitsch RM, Blatchford GJ, Thorson A, Christensen MA. Rare pelvic floor hernias. Report of a case and review of the literature. Dis Colon Rectum. 1992;35(6):604‐612. [DOI] [PubMed] [Google Scholar]
  • 2. Pearl RK, Nyhus LM, Condon RE, eds. Perineal hernia Hernia. 3rd ed. Philadelphia, PA: Lippincott; 1989:442‐446. [Google Scholar]
  • 3. Stamatiou D, Skandalakis JE, Skandalakis LJ, Mirilas P. Perineal hernia. Surgical anatomy, embryology, and technique of repair. Am Surg. 2010;76:474‐479. [PubMed] [Google Scholar]
  • 4. Thomas TG. Vulvar and vaginal enterocele. NY Med J. 1885;42:705‐711. [Google Scholar]
  • 5. Wilensky AO, Kaufman PA. Vaginal hernia. Am J Surg. 1940;49:31‐41. [Google Scholar]
  • 6. Ekberg O, Nordblom I, Fork FT, Gullmo A. Herniography of femoral, obturator and perineal hernias. Röfo. 1985;143:193‐199. [DOI] [PubMed] [Google Scholar]
  • 7. Sorelli PG, Clark SK, Jenkins JT. Laparoscopic repair of primary perineal hernias: the approach of choice in the 21st century. Colorectal Dis. 2011;14:72‐73. [DOI] [PubMed] [Google Scholar]
  • 8. Ghellai AM, Islam S, Stoker ME. Laparoscopic repair of postoperative perineal hernia. Surg Laparosc Endosc Percutan Tech. 2002;12:119‐121. [DOI] [PubMed] [Google Scholar]
  • 9. Franklin ME Jr, Abrego D, Parra E. Laparoscopic repair of postoperative perineal hernia. Hernia. 2002;6:42‐44. [DOI] [PubMed] [Google Scholar]
  • 10. Taichiro S, Shigehiko N, Seiji M, et al. Surgical technique of perineal hernia. Operation. 1979;38:115‐119. [Google Scholar]

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