Congenital Mullerian duct malformations are a challenging group of conditions for surgeons and need surgical experience and skill. Accordingly, the aim of this study is to present the diagnosis, surgical management, and clinical implications of congenital uterovaginal abnormalities.
Between 1980 and 2015, 8 patients with congenital uterovaginal abnormalities were diagnosed. In one patient a unique case of an unusual horseshoe shaped double uterus communicating via a transverse canal along with agenesis of the cervix and vagina was noted, and utero-vaginal agenesis was diagnosed in 6 patients. Complete androgen insensitivity syndrome with its female phenotype associated with bilateral testicular tissue in the inguinal canal with an accompanying absence of the ovaries, uterus, uterine tubes, vagina, and an imperforate hymen, was diagnosed in one patient. Clinical examination of all the patients revealed well-developed secondary sexual characteristics. A modified McIndoe vaginoplasty procedure was the surgical treatment common to all patients to treat vaginal agenesis. The surgery was performed by a consultant (Dr. K.G. Paul) using the standardized surgical technique.
An unusual Mullerian duct anomaly, uterus bicornisacollis, was successfully corrected by uteroplasty and a new cervix was constructed. Complete vaginal agenesis was corrected by a modified McIndoe vaginoplasty technique. None of the patients had any significant post-operative complications.
Knowledge of congenital uterovaginal abnormalities diagnosed in this study is essential for surgeons, clinical anatomists, radiologists, and morphologists who may increase the success of their diagnostic evaluations and surgical approaches to the region.
The reproductive system or genital system is a system of sex organs within an organism involved in producing offspring. In men, the genital system includes the prostate, testes, and penis. In women, it includes the ovaries, fallopian tubes, uterus, and vagina. A basic understanding of the embryology of the reproductive tract is essential to restore reproductive and sexual functioning and normalize genital anatomy whenever possible.
The vagina is the elastic, muscular part of the female genital tract, which extends from the vulva to the cervix. In humans, the vagina receives sperms during sexual intercourse, is the channel for the birth canal during the birth process, and also functions as an excretory channel for menstrual flow. Congenital vaginal agenesis is a rare malformation estimated to occur among 1 in 4,000–5,000 female births. The McIndoe technique was first described in 1938 by Bainster and McIndoe as a surgical procedure that improves quality of life and sexual satisfaction and provides a functional vagina with minimal complications for most patients with vaginal agenesis. Congenital and acquired genital anomalies in the adolescent population may lead to difficulties in carrying a pregnancy to term, infertility, and recurrent pregnancy loss, which lead to a great amount of social inhibition and psychological distress for the affected individuals. Such abnormalities are a challenging group of conditions for the reproductive surgeon and need surgical experience and skill. They also require a basic knowledge of the embryology of the reproductive tract to increase the success of diagnostic evaluations and surgical approaches to the region. Accordingly, the aim of this study was to evaluate congenital uterovaginal abnormalities, and their embryogenesis, surgical management, and clinical implications.
Between 1980 and 2015, 8 patients with congenital uterovaginal malformation were diagnosed in our clinics.
A 20-year-old unmarried woman presenting with primary amenorrhea was admitted to the Gynaecology Clinic of Princess Marine Hospital, Gaborone, Botswana. A diagnostic laparoscopy procedure revealed a double uterus, with communication via a transverse canal, along with agenesis of the cervix, vagina, and external vaginal opening (hymen). The urethral orifice was normal and the patient had well-developed secondary sexual characteristics.
Surgical correction (uteroplasty) of a uterine malformation (
Six unmarried woman (age 19–23 years) presented with primary amenorrhea. Diagnostic laparoscopy procedures revealed the presence of well-developed ovaries with an absence of a vagina, hymen, uterus, and uterine tubes. The urethral orifice was normal with well-developed secondary sexual characteristics. In all 3 patients, McIndoe vaginoplasty was performed to treat vaginal agenesis. Out of 6 patients, one was operated at INHS Asvini, Mumbai between 1980 and 1983, 3 patients were operated at 166 Military Hospital, Jammu between 1993 and 1995, and 2 patients were operated at Command Hospital, Calcutta during between 2000 and 2003(
A 20-year-old unmarried woman presenting with primary amenorrhea was admitted to the Gynaecology Department at the 166 Military Hospital, Jammu. A diagnostic laparoscopy procedure revealed the presence of bilateral testicular tissue (testicular feminization with its female phenotype) in the inguinal canal with an absence of ovaries, uterus, uterine tubes, and vagina, and an imperforate hymen. The urethral orifice and the external genitalia were normal. With the help of a geneticist, the karyotype was mapped and revealed a female phenotype, 46, XY. The testes were removed in order to avoid a risk of malignancy (
To treat vaginal agenesis, 7 patients (caseI and caseII) aged between 19 to 23 years underwent McIndoe vaginoplasty. The patients were operated on under general anaesthesia and placed in a lithotomic position with urinary catheterization (
An unusual Mullerian duct anomaly, uterus bicornis (double uterus) acollis (absence of cervix), was successfully corrected by uteroplasty and a new cervix was constructed. Complete vaginal agenesis in 7 patients was corrected by a modified McIndoe vaginoplasty technique. Clinical examination performed postoperatively revealed a neovagina of adequate length and caliber. None of the 7 patients had any significant post-operative complications.
The genital system is concerned with the maintenance and propagation of the species. In women, the internal genitalia include ovaries, fallopian tubes, the uterus, and the vagina; the external genitalia include mons pubis, labia majora and minora, the clitoris, the vestibule, and the perineum. Gonads initially develop in females (ovaries) and males (testes) from the undifferentiated genital ridge at approximately the 5th week of development, and gonadal differentiation becomes apparent at approximately the 7th week of embryonic life. In embryos of both sexes, the primitive sex ducts are indifferent and consist of 2 paired ducts—mesonephric (Wolffian) and paramesonephric (Mullerian). With the development of the testis from the genital ridge, the mesonephric duct is retained in males as the duct system of the testis and the paramesonephric duct mostly degenerates. In females, however, the paramesonephric duct plays an important role in the development of reproductive organs and the mesonephric duct and its tubules mostly regress.
At first, these paired bilateral Mullerian ducts pass caudally (through the cranial vertical part), lateral to the mesonephric duct. In the pelvis, they cross (through the intermediate horizontal part) ventral to the mesonephric duct and grow medially. During the 8th week, they reach the caudal end of the mesonephric duct and to contact and fuse with their counterparts (caudal vertical part) to form a Y shaped uterovaginal bulb or tubercle that bulges into the dorsal of the urogenital sinus. Caudal vertical parts of both Mullerian ducts fuse in the caudo-cranial direction, which normally occurs between the 6th and 11th weeks of gestation. The partition between them completely disappears and forms a single duct uterovaginal canal by the end of 3rd month. The cranial part of the utero-vaginal canal forms the entire uterus, and points of fusion of the 2 ducts represent the site of the future fundus. The cranial vertical parts and most of the intermediate horizontal parts of each Mullerian duct form the respective fallopian tubes. Any disruption of Mullerian duct development and fusion during embryogenesis can result in a broad and complex spectrum of congenital abnormalities, termed Mullerian duct anomalies. A uterus is absent in 2% to 7% of patients with vaginal agenesis [
The upper four-fifth of the vagina above the hymen develops from the lower part of the utero-vaginal canal and the lower one fifth develops below the hymen from the ectoderm of the genital folds. The vagina opens into the exterior through the vestibule, which is derived from the ectoderm of genital folds after the rupture of the urogenital membrane. Vaginal agenesis (absence of the vagina) is one of the most significant congenital anomalies of the female reproductive tract from a physical and psychological perspective. Vaginal agenesis is estimated to occur in 1 in 4,000–5,000 live female births. The purpose of vaginal agenesis treatment and appropriate management is not only to create an adequate passageway for penetration but also to facilitate satisfactory sexual intercourse and normalize genital anatomy where possible, and to alleviate her psychological concerns. To treat vaginal agenesis, the McIndoe technique is the preferred method for vaginal reconstruction, and several authors have documented satisfactory sexual relationships using the McIndoe method in over 75% of patients [
The sex-determining region Y (SRY) gene is located on the short arm of the Y chromosome. During the 6th week of male fetal development, the SRY gene provides instructions for making a protein called the SRY protein (testis determining factor) that influences the development of male phenotypes, such as testes from the genital ridges at the medial posterior abdominal cavity. Complete androgen insensitivity syndrome (testicular feminization) is a syndrome when a male, genetically XY, because of various abnormalities of the X chromosome, is resistant to the actions of androgen hormones, which in turn stops the forming of the male genitalia and gives a female phenotype. This syndrome occurs in one out of 20,000 live births and can be incomplete (various sexual ambiguities) or complete (the person appears to be a woman).Testicular feminization, or androgen insensitivity, is a rare syndrome that is characterized by primary amenorrhea, a 46, XY karyotype, a female phenotype, and the presence of testes rather than ovaries [
In conclusion, the findings suggested that a modified McIndoe vaginoplasty technique is a simple, effective procedure for the treatment of vaginal agenesis. We believe that the present study has provided some important data that will contribute to the scientific literature, providing the data of embryogenesis, surgical management, and clinical implications of uterovaginal congenital abnormalities. Awareness of the rare congenital abnormalities noted in our study is essential for surgeons, clinical anatomists, radiologists, and morphologists to increase the success of reproductive diagnostic evaluation and surgical approaches to the region.
No potential conflict of interest relevant to this article was reported.
This study was reviewed and approved by the appropriate institutional human research ethics committee (reference number: HREC10AUG19).
Each patient's informed consent for the purpose of this study (i.e. publication without disclosure of personal identity) was obtained.
Supplementary Figures associated with this article can be found online at
Intraoperative photograph showing uterine malformation and uteroplasty; 1 and 2, double uterus; 3, transverse canal; 4, ovaries; 5, fallopian tubes; A, uteroplasty.
Photographs showing congenital absence of the vagina; 1, vagina.
Photographs of patients (A, B) with complete androgen insensitivity syndrome with well-developed secondary sexual characteristics. The patient has a 46, XY karyotype and bilateral testicular tissue in the inguinal canal with an absence of ovaries, uterus, uterine tubes, vagina, and an imperforate hymen.
Intraoperative photographs showing McIndoe vaginoplasty. (A) Urinary catheterization under anaesthesia; 1, congenital absence of the vagina. (B) Mould lined by the full-thickness skin graft. (C) Mould lined by the full-thickness skin graft inserted into the newly constructed vaginal space.
Intraoperative photograph showing harvesting full-thickness skin grafts. (A, B) Bilateral harvesting of full-thickness skin grafts, (C) wound was closed and sutured (after harvesting the full-thickness skin graft) using a synthetic absorbable suture.