Anatomical variations, treatment and outcomes of Herlyn-Werner-Wunderlich syndrome: a literature review of 1673 cases

review OA: closed CC0
AI-generated summary by claude@2026-06+body, 2026-06-08

This systematic review of 1673 Herlyn-Werner-Wunderlich syndrome cases found dysmenorrhea and uterine didelphys were common, with vaginal septum excision being the primary effective treatment and a satisfactory pregnancy rate post-surgery.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-08 · read from full text

This paper is a systematic review of 1673 reported cases of Herlyn–Werner–Wunderlich syndrome (HWWS) using a structured search of PubMed, Scopus, Embase, and CNKI (2000 to April 19, 2022), extracting symptom prevalence, anatomical classifications/variants, treatment details, and short- and long-term outcomes. The most common symptoms were dysmenorrhea (53.8%), abnormal uterine bleeding (28.9%), and vaginal discharge (26.6%), while the principal anomalies included right obstructed hemivagina (57.3%), haematocolpos (81.7%), uterus didelphys (88.8%), and ipsilateral renal agenesis (93.1%); vaginal septum excision was the main treatment (91.8%) and only a small fraction required second surgery (2.2%). Endometriosis was reported in 9.6% of patients (with 52% having ipsilateral ovarian endometriosis cysts), and among those with endometriosis the reported pregnancy rate was 72.1% with 22.4% adverse pregnancy outcomes after surgery. A key limitation is that the work synthesizes published case data across many studies, which can affect consistency of reporting, and the authors note that further research is needed to clarify the relationship between pelvic endometriosis and HWWS. This paper is centrally about endometriosis and HWWS — it quantifies endometriosis prevalence in HWWS and highlights HWWS’s contribution to endometriosis, while calling for further investigation of their relationship.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

PURPOSE: This study aimed to perform a systematic review of patients with Herlyn-Werner-Wunderlich syndrome (HWWS) and present the prevalence of symptoms, anatomical variants, endometriosis, surgical interventions, and short- and long-term outcomes. METHODS: A structured search was performed in PubMed, Scopus, Embase, and China National Knowledge Infrastructure, and studies published between 1 January, 2000 and 19 April, 2022 were included. The following data on HWWS were recorded: symptoms, anatomical variations, surgical interventions and short- and long-term outcomes. RESULTS: A total of 1673 patients were included in our analysis. The main symptoms were dysmenorrhea (53.8%), abnormal uterine bleeding (28.9%), and vaginal discharge (26.6%). The principal anomalies were right-obstructed hemivagina (57.3%), haematocolpos (81.7%), uterus didelphys (88.8%), and ipsilateral renal agenesis (93.1%). A majority of patients belonged to classification 1.1 (46.7%), with a blind hemivagina, and classification 2.1 (39.2%), with a small communication between two vaginas. The mainstay of treatment was vaginal septum excision (91.8%). Minimally invasive surgery (48.5%) was performed only after vaginal surgery (61.9%), and only a few patients required a second surgery (2.2%). Endometriosis was found in 9.6% of the patients. Fifty-two percent of them had ipsilateral ovarian endometriosis cysts. Pregnancy rate of these patients was 72.1%. The rate of adverse pregnancy outcomes was 22.4%. The caesarean section rate was 61.2%. CONCLUSIONS: Patients with HWWS presented with nonspecific symptoms and demonstrated various combinations of anomalies. The most common anatomical variants are classifications 1.1 and 2.1. Vaginal septum excision is effective in relieving symptoms and preventing complications, with hysteroscopic surgery as an option where there is concern about protecting the hymen from minor injury. The pregnancy rate for these patients after surgery was satisfactory, and the rate of adverse pregnancy outcomes after surgery was acceptable. We advise females with urological anomalies to be screened for Müllerian anomalies because of the close association between these two types of anomalies. Thus, HWWS contributes to the occurrence of endometriosis; however, more research is required to investigate the relationship between pelvic endometriosis and HWWS.
Full text 13,035 characters · extracted from oa-doi-fallback · 6 sections · click to expand

Abstract

Purpose This study aimed to perform a systematic review of patients with Herlyn–Werner–Wunderlich syndrome (HWWS) and present the prevalence of symptoms, anatomical variants, endometriosis, surgical interventions, and short- and long-term outcomes.

Methods

A structured search was performed in PubMed, Scopus, Embase, and China National Knowledge Infrastructure, and studies published between 1 January, 2000 and 19 April, 2022 were included. The following data on HWWS were recorded: symptoms, anatomical variations, surgical interventions and short- and long-term outcomes.

Results

A total of 1673 patients were included in our analysis. The main symptoms were dysmenorrhea (53.8%), abnormal uterine bleeding (28.9%), and vaginal discharge (26.6%). The principal anomalies were right-obstructed hemivagina (57.3%), haematocolpos (81.7%), uterus didelphys (88.8%), and ipsilateral renal agenesis (93.1%). A majority of patients belonged to classification 1.1 (46.7%), with a blind hemivagina, and classification 2.1 (39.2%), with a small communication between two vaginas. The mainstay of treatment was vaginal septum excision (91.8%). Minimally invasive surgery (48.5%) was performed only after vaginal surgery (61.9%), and only a few patients required a second surgery (2.2%). Endometriosis was found in 9.6% of the patients. Fifty-two percent of them had ipsilateral ovarian endometriosis cysts. Pregnancy rate of these patients was 72.1%. The rate of adverse pregnancy outcomes was 22.4%. The caesarean section rate was 61.2%.

Conclusions

Patients with HWWS presented with nonspecific symptoms and demonstrated various combinations of anomalies. The most common anatomical variants are classifications 1.1 and 2.1. Vaginal septum excision is effective in relieving symptoms and preventing complications, with hysteroscopic surgery as an option where there is concern about protecting the hymen from minor injury. The pregnancy rate for these patients after surgery was satisfactory, and the rate of adverse pregnancy outcomes after surgery was acceptable. We advise females with urological anomalies to be screened for Müllerian anomalies because of the close association between these two types of anomalies. Thus, HWWS contributes to the occurrence of endometriosis; however, more research is required to investigate the relationship between pelvic endometriosis and HWWS. Similar content being viewed by others Data availability Data sharing is not applicable—All data in this paper were public.

References

Purslow CE (1922) A case of unilateral hæmatokolpos, hæmatometra and hæmatosalpinx, BJOG. Int J Obstet Gynaecol 29:643. https://doi.org/10.1111/j.1471-0528.1922.tb16100.x Herlyn U, Werner H (1971) Simultaneous occurrence of an open Gartner-duct cyst, a homolateral aplasia of the kidney and a double uterus as a typical syndrome of abnormalities. Geburtshilfe Frauenheilkd 31:340–347 Wunderlich M (1976) Unusual form of genital malformation with aplasia of the right kidney. Zentralbl Gynakol 98:559–562 Karag”ozov I (1983) Herlyn-Werner-Wunderlich syndrome. Akush Ginekol (Sofiia) 22:70–76 Kudela G, Wiernik A, Drosdzol-Cop A, Machnikowska-Sokołowska M, Gawlik A, Hyla-Klekot L, Gruszczyńska K, Koszutski T (2021) Multiple variants of obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome—one clinical center case series and the systematic review of 734 cases. J Pediatr Urol 17:653.e651-653.e659. https://doi.org/10.1016/j.jpurol.2021.06.023 Burgis J (2001) Obstructive Mullerian anomalies: case report, diagnosis, and management. Am J Obstet Gynecol 185:338–344. https://doi.org/10.1067/mob.2001.116738 Sanchez-Ferrer ML, Acien MI, Sanchez del Campo F, Mayol-Belda MJ, Acien P (2006) Experimental contributions to the study of the embryology of the vagina. Hum Reprod 21:1623–1628. https://doi.org/10.1093/humrep/del031 Vercellini P, Daguati R, Somigliana E, Vigano P, Lanzani A, Fedele L (2007) Asymmetric lateral distribution of obstructed hemivagina and renal agenesis in women with uterus didelphys: institutional case series and a systematic literature review. Fertil Steril 87:719–724. https://doi.org/10.1016/j.fertnstert.2007.01.173 Fascilla FD, Olivieri C, Cannone R et al (2020) In-office hysteroscopic treatment of Herlyn-Werner-Wunderlich syndrome: a case series. J Minim Invasive Gynecol 27:1640–1645. https://doi.org/10.1016/j.jmig.2020.04.013 Gungor Ugurlucan F, Dural O, Yasa C, Kirpinar G, Akhan SE (2020) Diagnosis, management, and outcome of obstructed hemivagina and ipsilateral renal agenesis (OHVIRA syndrome): is there a correlation between MRI findings and outcome? Clin Imaging 59:172–178. https://doi.org/10.1016/j.clinimag.2019.11.013 Yang M, Wen S, Liu X et al (2021) Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA): early diagnosis, treatment and outcomes. Eur J Obstet Gynecol Reprod Biol 261:12–16. https://doi.org/10.1016/j.ejogrb.2021.03.018 Albulescu DM, Ceauşescu AE, Sas LM, Comănescu MC, Constantin C, Tudorache Ş (2018) The Herlyn-Werner-Wunderlich triad (OHVIRA syndrome) with good pregnancy outcome—two cases and literature review. Rom J Morphol Embryol 59:1253–1262 Tuna T, Estevão-Costa J, Ramalho C, Fragoso AC (2019) Herlyn-Werner-Wunderlich syndrome: report of a prenatally recognised case and review of the literature. Urology 125:205–209. https://doi.org/10.1016/j.urology.2018.12.022 Zhu L, Chen N, Tong JL, Wang W, Zhang L, Lang JH (2015) New classification of Herlyn-Werner-Wunderlich syndrome. Chin Med J (Engl) 128:222–225. https://doi.org/10.4103/0366-6999.149208 Han JH, Lee YS, Im YJ, Kim SW, Lee MJ, Han SW (2016) Clinical implications of obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome in the prepubertal age group. PLoS ONE. https://doi.org/10.1371/journal.pone.0166776 Kim YN, Han JH, Lee YS, Lee I, Han SW, Seo SK, Yun BH (2021) Comparison between prepubertal and postpubertal patients with obstructed hemivagina and ipsilateral renal anomaly syndrome. J Pediatr Urol 17:652.e651-652.e657. https://doi.org/10.1016/j.jpurol.2021.06.008 Noviello C, Romano M, Nino F, Martino A, Cobellis G (2018) Clinical and radiological findings for early diagnosis of Herlyn-Werner-Wunderlich syndrome in pediatric age: experience of a single center. Gynecol Endocrinol 34:56–58. https://doi.org/10.1080/09513590.2017.1332178 Tan YG, Laksmi NK, Yap TL, Sadhana N, Ong CCP (2020) Preventing the O in OHVIRA (obstructed hemivagina ipsilateral renal agenesis): early diagnosis and management of asymptomatic Herlyn-Werner-Wunderlich syndrome. J Pediatr Surg 55:1377–1380. https://doi.org/10.1016/j.jpedsurg.2019.06.006 Song ZN, Tang DX, Wu DH, Huang Y, Tao C, Chen GJ, Wang XH, Yang RL (2019) Clinical characteristics of children with Herlyn-Werner-Wunderlich syndrome. Chin J Pediatr Surg 40:456–459. https://doi.org/10.3760/cma.j.issn.0253-3006.2019.05.015 Li L, Chu C, Li S et al (2021) Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome. Fertil Steril 116:1360–1369. https://doi.org/10.1016/j.fertnstert.2021.06.033 Zhang J, Zhang M, Zhang Y, Liu H, Yuan P, Peng X, Cao Z, Wang L (2020) Proposal of the 3O (obstruction, ureteric orifice, and outcome) subclassification system associated with obstructed hemivagina and ipsilateral renal anomaly (OHVIRA). J Pediatr Adolesc Gynecol 33:307–313. https://doi.org/10.1016/j.jpag.2020.01.001 Zhang J, Xu S, Yang L, Songhong Y (2020) MRI image features and differential diagnoses of Herlyn–Werner–Wunderlich syndrome. Gynecol Endocrinol 36:484–488. https://doi.org/10.1080/09513590.2019.1680623 Smith NA, Laufer MR (2007) Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome: management and follow-up. Fertil Steril 87:918–922. https://doi.org/10.1016/j.fertnstert.2006.11.015 Candiani GB, Fedele L, Candiani M (1997) Double uterus, blind hemivagina, and ipsilateral renal agenesis: 36 cases and long-term follow-up. Obstet Gynecol 90:26–32. https://doi.org/10.1016/S0029-7844(97)83836-7 Heinonen PK (2000) Clinical implications of the didelphic uterus: long-term follow-up of 49 cases. Eur J Obstet Gynecol Reprod Biol 91:183–190. https://doi.org/10.1016/s0301-2115(99)00259-6 Hamidi H, Haidary N (2018) Late presentation, MR imaging features and surgical treatment of Herlyn-Werner-Wunderlich syndrome (classification 2.2); a case report. BMC Womens Health 18:161. https://doi.org/10.1186/s12905-018-0655-4 Piriyev E, Romer T (2020) Coincidence of uterine malformations and endometriosis: a clinically relevant problem? Arch Gynecol Obstet 302:1237–1241. https://doi.org/10.1007/s00404-020-05750-9 Giudice LC, Kao LC (2004) Endometriosis. Lancet 364:1789–1799. https://doi.org/10.1016/S0140-6736(04)17403-5 Bulletti C, Coccia ME, Battistoni S, Borini A (2010) Endometriosis and infertility. J Assist Reprod Genet 27:441–447. https://doi.org/10.1007/s10815-010-9436-1 Fedele L, Bianchi S, Di Nola G, Franchi D, Candiani GB (1992) Endometriosis and nonobstructive mullerian anomalies. Obstet Gynecol 79:515–517 Fedele L, Motta F, Frontino G, Restelli E, Bianchi S (2013) Double uterus with obstructed hemivagina and ipsilateral renal agenesis: pelvic anatomic variants in 87 cases. Hum Reprod 28:1580–1583. https://doi.org/10.1093/humrep/det081 Tong J, Zhu L, Chen N, Lang J (2014) Endometriosis in association with Herlyn-Werner-Wunderlich syndrome. Fertil Steril 102:790–794. https://doi.org/10.1016/j.fertnstert.2014.05.025 Tong J, Zhu L, Lang J (2013) Clinical characteristics of 70 patients with Herlyn-Werner-Wunderlich syndrome. Int J Gynaecol Obstet 121:173–175. https://doi.org/10.1016/j.ijgo.2012.11.023 Ugur M, Turan C, Mungan T, Kuscu E, Senoz S, Agis HT, Gokmen O (1995) Endometriosis in association with mullerian anomalies. Gynecol Obstet Invest 40:261–264. https://doi.org/10.1159/000292349 Del Vescovo R, Battisti S, Di Paola V, Piccolo CL, Cazzato RL, Sansoni I, Grasso RF, Zobel BB (2012) Herlyn-werner-wunderlich syndrome: MRI findings, radiological guide (two cases and literature review), and differential diagnosis. BMC Med Imaging. https://doi.org/10.1186/1471-2342-12-4 The American Fertility Society classifications of adnexal adhesions (1988) distal tubal occlusion, tubal occlusion secondary to tubal ligation, tubal pregnancies, mullerian anomalies and intrauterine adhesions. Fertil Steril 49:944–955. https://doi.org/10.1016/s0015-0282(16)59942-7 Grimbizis GF, Gordts S, Di Spiezio SA et al (2013) The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies. Hum Reprod 28:2032–2044. https://doi.org/10.1093/humrep/det098 Jayasinghe Y, Rane A, Stalewski H, Grover S (2005) The presentation and early diagnosis of the rudimentary uterine horn. Obstet Gynecol 105:1456–1467. https://doi.org/10.1097/01.AOG.0000161321.94364.56 Zhang H, Pan H (2021) Hysteroscopic management of an oblique vaginal septum with diverticulum in Herlyn-Werner-Wunderlich syndrome. J Minim Invasive Gynecol 28:1553–1554. https://doi.org/10.1016/j.jmig.2021.03.009 Chen C, Lei P, Zhang Y et al (2020) Value of contrast-enhanced mr imaging for evaluation of diagnosis and classification in oblique vaginal septum syndrome. J Clin Radiol. 39:2037–2041. https://doi.org/10.13437/j.cnki.jcr.2020.10.029 Long Q, Zhang Y, Zhang J, Tang X, Kingdon C (2022) Changes in caesarean section rates in China during the period of transition from the one-child to two-child policy era: cross-sectional national household health services surveys. BMJ Open 12:e059208. https://doi.org/10.1136/bmjopen-2021-059208

Acknowledgements

We appreciated the encouragements from Wei Chen. Funding This research did not receive any grants or funds. Author information Authors and Affiliations Contributions Conceptualization: YDL. Literature search and Data analysis: YL, ZL. Writing—original draft preparation: YL, ZL and JW. Writing—review & editing. YL, YD and YDL. All authors have read and agreed to the published version of the manuscript. Corresponding author Ethics declarations Conflict of interest The authors declare that they have no conflict of interest. Ethical approval IRB approval was not required. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Liu, Y., Li, Z., Dou, Y. et al. Anatomical variations, treatment and outcomes of Herlyn-Werner-Wunderlich syndrome: a literature review of 1673 cases. Arch Gynecol Obstet 308, 1409–1417 (2023). https://doi.org/10.1007/s00404-022-06856-y Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s00404-022-06856-y

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosis

MeSH descriptors

Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple Abnormalities, Multiple

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (41)

Source provenance

europepmc
last seen: 2026-06-11T06:19:48.454388+00:00
openalex
last seen: 2026-06-04T00:00:01.174412+00:00
pubmed
last seen: 2026-06-11T06:18:57.514842+00:00
unpaywall
last seen: 2026-06-04T02:00:05.705006+00:00
License: CC0 · commercial use OK