Diagnosis approach, treatment, evaluation and fertility preservation in patient with Herlyn-Werner-Wunderlich syndrome: a case report

https://doi.org/10.19106/JMedSci005504202308

Lathifa Nadhya Indraswari(1), Nuring Pangastuti(2*), Akbar Novan Dwi Saputra(3), Anis Widyasari(4)

(1) Departement of Obstetry Ginekology Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta
(2) Departement of Obstetry Ginekology Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta
(3) Departement of Obstetry Ginekology Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta
(4) Departement of Obstetry Ginekology Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta
(*) Corresponding Author

Abstract


Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare female congenital anomaly of urogenital tract. The definite etiology of HWW syndrome is still unknown. It may be caused by the abnormal development of Mullerian and Wolffian ducts. The characteristic triad of this syndrome includes didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis, recently known as Obstructed Hemivagina and Ipsilateral Renal Anomaly (OHVIRA) syndrome.  A 17 y.o. presented with intermittent lower abdominal pain. Physical examination revealed in normal limit. From the ultrasonography examination, it was found uterus didelphys with left hemiuterus hematomethra, hematocolpos, with normal anatomy and function of the right kidney, but there was no left kidney. From pelvic magnetic resonance imaging (MRI) and laparoscopy showing a complete duplication of the uterus from the horn to the cervix with no connection between the two uterine cavities. Both ovaries were normal. The right fallopian tube was normal. The left tube was enlarged, attached to the uterus and the left ovary. No left kidney was found.  From the previous surgery, there was a misdiagnosed with brown cyst. Physical examination such as rectal toucher often missed, regardless it can be used to determine some differential diagnosis. MRI is most accurate for providing details regarding the altered anatomy and for identifying associated hematocolpos, hematosalping or hematometra for HWW syndrome cases. The laparoscopy guiding diagnostic and operative management of the vaginal septectomy procedure was performed. In conclusion,  misdiagnosis of HWW syndrome can be occurred on ultrasound examination. MRI is an examination that is considered appropriate to help confirm the diagnosis. Laparoscopy can be used with the aim of establishing a diagnosis or in surgical management, in this case, a septectomy is performed.


Keywords


Herlyn-Werner-Wunderlich syndrome; obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome; diagnosis; MRI; septectomi

Full Text:

PDF


References


1. David A, Gudi SN, Shankar R. Herlyn–Werner–Wunderlich syndrome: premenarche. J South Asian Feder Obstet Gynaecol 2017; 9(2):207-10.
https://doi.org/10.5005/jp-journals-10006-1496
2. Zhu L, Chen N, Tong JL, Wang W, Zhang L, Lang JH. New classification of Herlyn-Werner-Wunderlich syndrome. Chin Med J (Engl) 2015; 128(2):222-5.
https://doi.org/10.4103/0366-6999.149208
3. Anonym. Management of acute obstructive uterovaginal anomalies: ACOG Committee Opinion No. 779. Obstet Gynecol 2019; 133(6):e363-71.
https://doi.org/10.1097/AOG.0000000000003281
4. Liang HI, Fu SC, Yin CH, Chang CC. Herlyn–Werner–Wünderlich syndrome: an unusual case with presentation of menorrhagia. Taiwan J Obstet Gynecol 2020; 59(6):948-51.
https://doi.org/10.1016/j.tjog.2020.09.026
5. Del Vescovo R, Battisti S, Di Paola V, Piccolo CL, Cazzato RL, Sansoni I, et al. Herlyn-Werner-Wunderlich syndrome: MRI findings, radiological guide (two cases and literature review), and differential diagnosis. BMC Med Imaging 2012; 12:4.
https://doi.org/10.1186/1471-2342-12-4
6. Gholoum S, Puligandla PS, Hui T, Su W, Quiros E, Laberge JM. Management and outcome of patients with combined vaginal septum, bifid uterus, and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome). J Pediatr Surg 2006; 41(5):987-92.
https://doi.org/10.1016/j.jpedsurg.2006.01.021
7. Park NH, Park HJ, Park CS, Park SI. Herlyn-Werner-Wunderlich Syndrome with unilateral hemivaginal obstruction, ipsilateral renal agenesis, and contralateral renal thin GBM disease: a case report with radiological follow-up. J Korean Soc Radiol 2010; 62(4):383-8.
https://doi.org/10.3348/jksr.2010.62.4.383
8. Behr SC, Courtier JL, Qayyum A. Imaging of müllerian duct anomalies. Radiographics 2012; 32(6):E233-50.
https://doi.org/10.1148/rg.326125515
9. Pittokopitou S, Kathopoulis N, Protopapas A, Domali E. Herlyn–Werner–Wunderlich syndrome: report of a delayed diagnosed case with video presentation of the operative technique of vaginal septum resection. J Obstet Gynaecol Res 2021; 47(6):2242-5
https://doi.org/10.1111/jog.14743
10. Khaladkar SM, Kamal V, Kamal A, Kondapavulur SK. The Herlyn-Werner-Wunderlich syndrome – a case report with radiological review. Pol J Radiol 2016; 81:395-400
https://doi.org/10.12659/PJR.897228
11. Dias JL, Jogo R. Herlyn-Werner-Wunderlich syndrome: pre-and post-surgical MRI and US findings. Abdom Imaging 2015; 40(7):2667-82.
Httpa://doi.org/10.1007/s00261-015-0421-0
12. Ahmad Z, Goyal A, Das CJ, Deka D, Sharma R. Herlyn-Werner-Wunderlich syndrome presenting with infertility: role of MRI in diagnosis. Indian J Radiol Imaging 2013; 23(3):243-6.
https://doi.org/10.4103/0971-3026.120283
13. Wdowiarz K, Skrajna A, Reinholz-Jaskólska M. Diagnosis and treatment of Herlyn-Werner-Wunderlich syndrome: a case report. Prz Menopauzalny 2021; 20(1):52-56.
https://doi.org/10.5114/pm.2021.104034
14. Moruzzi MC, Bolomini G, Albanese M, Catena U, Romito I, Fagotti A, et al. Intraoperative endoscopic ultrasound guided surgical treatment of Herlyn-Werner-Wunderlich syndrome: case report and a systematic literature review. Obstet Gynecol Res 2020; 3:037-80.
https://doi.org/10.26502/ogr033
15. Candenas LB, Davo DA, de Medina MPR, Orlando JM, Diaz ACL. Diagnosis and gestational follow-up in a patient with Herlyn-Werner-Wünderlich syndrome: a case report. Taiwan J Obstet Gynecol 2019; 58(4):560-5.
https://doi.org/10.1016/j.tjog.2019.05.023



DOI: https://doi.org/10.19106/JMedSci005504202308

Article Metrics

Abstract views : 1117 | views : 673




Copyright (c) 2023 Lathifa Nadhya Indraswari, Nuring Pangastuti, Akbar Novan Dwi Saputra, Anis Widyasari

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

FUJI188