Herlyn-Werner-Wunderlich Syndrome: A Case of Report and Literature Review

Background: Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare type of female reproduction tract malformation, often accompanied by abnormal development of the ipsilateral urinary system, which shows mostly double uterus and the absence of the kidney on the oblique side. Case Report: An 11-year-old patient presented with lower abdominal distension and pain for 2 days and was suspected of vaginal haematoma. Conclusion: Ipsilateral renal agenesis was confirmed by ultrasound during hospitalization, and the diagnoses of obstructed hemivagina and ipsilateral renal anomaly syndrome were established. The aim of this study was to present the diagnostic and therapeutic approaches in HWWS, and to draw attention to the challenges in its diagnosis, which can coexist with multiple complications.


Introduction
Herlyn-Werner-Wunderlich syndrome (HWWS; also known as Oblique vaginal septum syndrome, OVSS) is a kind of asymmetric genitourinary congenital malformations, including didelphys uterus, unilateral blind hemivagina, and ipsilateral renal agenesis, such as absence of one side of the kidney, which is more common in HWWS, heterotopic single kidney malformation, horseshoe kidney, etc. [1] [2]. Due to non-specific clinical manifestations, the rate of missed diagnosis and misdiagnosis is extremely high [3]. A case of HWWS patient admitted to the First Affiliated Hospital of Yangtze University, the First People's Hospital of Jingzhou is reported, combined with literature review, in order to strengthen clinicians' understanding of this syndrome, improve the diagnosis rate of HWWS, and improve the prognosis of patients.

Case Presentation
The patient was a 11-year-old unmarried woman with no history of sexual activity, and had menstrual cramps in January 2021. The first three menstrual cycles after menstruation are regular, but menstrual volume in the recent 2 months is less, and there is no dysmenorrhea. She experienced lower abdominal distension and paroxysmal pain, aggravated when cold and occasionally aggravated sensation during defecation since two days ago. Her pain did not radiate and was not associated with chills, fever, nausea, vomiting, abdominal pain, diarrhea and other discomforts. The symptoms of lower abdomen distension are significantly relieved than before, and she has not complained of any special discomfort, she came to our hospital for treatment. Gynecological examination showed that the vulva development was normal, and a purple-blue spherical mass of about 2 × 3 cm in size was visible at the vaginal opening. The tension was slightly high, and internal consultation was not performed. Transabdominal sonography showed that the uterine morphology is abnormal, and two uterine echoes can be seen in   prevention, fluid rehydration, and symptomatic treatment are given. Oblique incision through the vagina, the symptoms of the patient disappeared quickly, and the prognosis was good. She has recovered well and has been discharged from hospital.

Pathogenesis
The incidence of HWWS is 0.1% -3.8%, and currently the pathogenesis is unclear [4]. The vagina is formed by the development and connection of the end of the accessory mesonephric duct and the urogenital sinus. On the embryonic side, the mesonephric duct and the accessory mesonephric duct are underdeveloped. They are not in contact with the urogenital sinus and cannot form an unobstructed vagina. The accessory mesonephros fusion fails, and the twin uterus, twin cervix and vaginal septum malformations develop respectively [5] [6]. The oblique vaginal septum is a membranous tissue that grows down from between the two cervixes, forming a blind cavity on one side obliquely to cover the cervix on this side. Current research shows that the mechanism of the asymmetric deformity of the oblique vaginal septum is still unclear, which may be related to the downward extension of the accessory mesonephric duct without contacting the urogenital sinus and the formation of a blind end [7] [8]. The urinary system and the reproductive system have a common origin. The development of the accessory mesonephric duct depends on the development of the mesoneph-ric duct. The dysplasia of the mesonephric duct often coexists with the dysplasia of the accessory mesonephric duct. Therefore, the malformation of the reproductive system is often accompanied by There are malformations of the urinary system. This disease is characterized by double uterus, double cervix, double vagina, complete or incomplete atresia of one side of the vagina, and often accompanied by absence of kidney and ureter on the oblique side. There are reports that the right kidney is absent, while this case is on the left side [9] [10].

Clinical Classification
At present, the classification of Peking Union Medical College Hospital is mostly used in China [11]. The deformity is divided into 3 types: type I (no Oblique endometriosis: rarely occurs, and may be related to long-term menstrual reflux [13]. This patient was 11 years old and had menarche. Because of her young age, the uterus, cervix, and vagina were not fully developed, so she could not perform transvaginal diagnosis. Gynecological examination was limited, and it was not easy to find positive signs in the vagina. The patient complained of pain in the lower abdomen, accompanied by ultrasound prompting a large amount of blood in the vagina, which is clinically very similar to hymen atresia. If only the obstruction of the lower genital tract is considered, the uterine development abnormality is missed and misdiagnosis is easy to occur. Clinically, patients with genital tract dysplasia with no menarche during adolescence and emergency treatment should be fully considered and fully evaluated before surgery. In particular, MRI can clearly diagnose vaginal oblique septum syndrome and assist in the evaluation of its clinical classification [12] [14] [15]. When a patient has one side of the kidney, especially in adolescent women, combined with genital malformations, pelvic masses, and primary dysmenorrhea, HWWS should be considered first.

Differential Diagnosis
Due to the diversity of clinical manifestations of HWWS, it is easy to be misdiagnosed. Clinically, it is easy to be confused with the following common diseases: 1) Functional uterine bleeding: In type II and III oblique septum syndrome, there is repeated irregular vaginal bleeding. 2) Pelvic inflammatory disease: When the oblique vaginal septum syndrome is repeatedly bleeding with infection, symptoms of pelvic inflammatory disease such as purulent vaginal discharge, fever, and abdominal pain may appear. 3) Pelvic mass: hemorrhage or empyema on the affected side, ectopic cyst, pelvic examination and color Doppler ultrasound can be mistaken for pelvic tumor or abscess. 4) Endometriosis: Patients with oblique vaginal septum syndrome have progressively aggravated dysmenorrhea due to poor menstrual blood drainage or menstrual blood reflux.
Color Doppler ultrasound suggests that there are dot-like dense echoes in the cyst, which is often confused with endometriotic cysts. 5) Others such as ectopic pregnancy, infertility, appendicitis, residual horn uterine bleeding (or pregnancy), vaginal wall cysts, etc., should sometimes be differentiated from HWWS [19]. HWWS I patients mainly present with dysmenorrhea, which is easily misdiagnosed as primary dysmenorrhea, vaginal wall cysts, and pelvic masses. Type II and Type III patients mainly manifested as vaginal bloody or purulent discharge, which is easily misdiagnosed as vaginitis, pelvic inflammatory disease, adolescent dysfunctional uterine bleeding, etc. [20].

Treatment
HWWS patients are mostly adolescents and women of childbearing age. The principle of treatment is to repair and reconstruct functions based on the type of genital tract malformations, try to protect the function and integrity of the organs, and relieve the obstruction of the outflow tract. Therefore, the minimally invasive hysteroscopy combined with vaginal oblique diaphragm resection has advantages. There are three kinds of surgical methods: oblique vaginal septum resection, oblique vaginal septum resection combined with hysteroscopy and hysterectomy in the posterior cavity. Oblique vaginal septum resection is the most fundamental surgical method for the treatment of HWWS. In type III patients, the cervical fistula should be repaired at the same time during the operation [4]. After the operation, the vagina was filled with iodophor gauze for 24 to 48 hours, and antibiotics were used to prevent infection. Potassium permanganate powder was bathed for 7 to 10 days [21].

Conclusion
All in all, the diagnosis of HWWS may currently be a challenge for gynecologists. Gynecologists, pediatricians, and radiologists should consider the differential diagnosis of HWWS in genital tract abnormalities to improve the diagnosis rate of HWWS. The uterus on the oblique side of the vagina may still be pregnant, and resection should be avoided as much as possible to improve the pa-tient's ability to conceive. Whether to remove the uterus on the oblique side of the vagina is still controversial. There are few follow-up cases of postoperative pregnancy in HWWS patients, and further samples need to be accumulated for analysis and summary. At present, the mechanism of the asymmetric deformity of the oblique vaginal septum is not fully understood, and further research is needed.

Ethical Approval and Consent to Participate
This work follows the guidelines for human studies and was conducted ethically in accordance with the World Medical Association Declaration of Helsinki. Written informed consent was obtained from the patient for reporting and publication of this case report and any accompanying images and the relevant approval was obtained from the ethical committee of the First Affiliated Hospital of Yangtze University.

Consent for Publication
The consent for publication was obtained from both the patient and the First Affiliated Hospital of Yangtze University.

Availability of Supporting Data
The data is stored in the electronic database of the First Affiliated Hospital of Yangtze University under the confidentiality act.

Author Contributions
H.J.L. developed the concept, collected the data, and wrote the manuscript. C.J.Y. participated in writing the manuscript. C.J.Y. analysed the data and coordinated efforts. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript.