Department of Obstetrics and Gynecology, Alkindi Specialized Hospital, Zinj, Kingdom of Bahrain
Received date: December 04, 2017; Accepted date: February 06, 2018; Published date: February 09, 2018
Citation: Al-Hubaishi F, Al-Najjar F, Al-Medfa AS (2018) A Case Report on an Asymptomatic Labial Fusion in a Woman of Reproductive Age. Gynecol Obstet Case Rep Vol.4:No.1:60. doi: 10.21767/2471-8165.1000060
Labial adhesions are extremely rare in reproductive age groups. Only a few cases were described in the literature. We report a female patient with an incidental finding of labial adhesions. The patient was a 24-year-old woman, not a known case of any medical illnesses, presented with asymptomatic labial adhesions, incidentally found on shaving. Clinical examination revealed normally developed Labia majora, adhered at the lower part just above the vaginal opening. Labia minora were partially but extensively fused, covering the clitoral hood. Intraoperatively, labial fusion was dissected with lectrocautery under general anesthesia. Postoperatively, on follow up, the adhesions were completely separated, and the area healed. No recurrence.
Labial fusion; Labial adhesion
Labial adhesion (also called labial agglutination and synechia vulvae) is a common vaginal condition estimated to occur in 0.6%-5% of prepubertal girls , with a peak incidence of up to 3 percent of girls in the second year of life  However, this condition is a rare clinical entity in adults ; only a few cases have been reported in the literature; predominantly occurring in postmenopausal women rather than in reproductive ages . Labial adhesions may be partial, involving only the upper or lower labia, or complete .
The majority of the reported cases are asymptomatic. Rarely, they may present with urinary incontinence, urinary tract infections, vaginitis, hematuria, dysuria or dyspareunia . The etiological factors reported to contribute to Labial adhesions are chronic vaginal inflammation, hypoestrogenism, lack of sexual activity, local trauma, circumcision, vaginal lacerations in childbirth, recurrent urinary tract infections and lichen sclerosus. Furthermore, labial adhesions can rarely occur idiopathically, without any evidence of the above [5,6]. In this article, we describe a case of extensive labial fusion as an incidental finding in an asymptomatic reproductive age woman, it’s management and literature review.
A 24-year-old, female presented to the outpatient Gynaecology department complaining of fused labia, that she incidentally found while shaving. The patient is asymptomatic; and is sexually inactive.
Gynecological examination revealed Extensive adhesion of the labia minora, covering the clitoral hood completely. The labia majora was normal in shape but fused at the lower border just above the vaginal opening. The urethral orifice and the vaginal opening were visualized and normal (Figure 1).
Urinalysis and urine culture were negative for infection. The patient was not investigated for any sexually transmitted diseases. Hormonal analysis revealed normal estrogen and gonadotropin levels as seen in Table 1.
Table 1: Results of the patient’s hormone assay.
Pelvic ultrasonography and MRI were not done. Under general anesthesia, in the lithotomy position, inspection of the external genitalia revealed fused labia minora, clitoral hood could not be retracted, and the surrounding vulva appeared white and atrophic. The degree of adhesion was such that the clitoral hood could not be seen.
The labia majora was partially fused at the lower border just above the vaginal opening. The Vaginal opening and the urethral orifice were visualized and normal. Labial adhesions were released by electrocautery and the released edges were sutured (Figure 2). A pack containing fusidic acid was applied for 24 hours.
Postoperatively, the patient was discharged with daily topical Fucidin ointment, to be applied for four weeks. Labia Minora over the clitoral hood was not released as it was extensively fused and atrophied. Reconstructive surgery is needed for such release (Figure 3).
On her postoperative follow up at the end of six weeks, labial tissues were found to be completely healed (Figure 4).
Labial fusion, a common vaginal condition in children, is a rare clinical entity in adults, occurring more rarely in reproductive age women. The relative hypoestrogenic environment and sexual abuse/genital trauma are suggested as the main predisposing factors of this disorder in prepubertal girls. As for adults, Labial fusion is associated with recurrent urinary tract infections, vulvovaginitis, genital trauma, hypoestrogenism and lack of sexual activity, with a few cases which were diagnosed as lichen sclerosis after punch biopsy [5,7].
We can exclude hypoestrogenemia as the cause of labial fusion in our patient with a history of regular menses. She did not state any history of sexual abuse or genital trauma either; both of which have been reported as possible causes of Labial fusion in reproductive age females. Despite the extensive adhesions, our patient was symptomatic. The general initial therapy for superficial labial adhesions is estrogen cream. Particularly, in prepubertal and postmenopausal women as it might reduce the irritation of the vaginal mucosa and hence aid in subsequent repair [8,9]. In patients with complete, thick adhesions and a long history of Labial fusion. Our patient’s age, status and her wish of expeditious treatment made us choose surgery instead of topical therapy. Complete healing was achieved in 6 weeks with no further complaints. As per the adhesions, our patient would have had sexual dysfunction/ dyspareunia if she was sexually active.
Labial fusion is a rare event in reproductive women. However, it should be considered in the differential diagnoses of the patients presenting with sexual dysfunction.
The woman whose story is told in this case report has provided signed permission for its publication.
All Published work is licensed under a Creative Commons Attribution 4.0 International License
Copyright © 2018 All rights reserved. iMedPub LTD Last revised : May 23, 2018