Successful Gestation of a Herlyn-Werner-Wunderlich Syndrome Carrier And Patient, After a Hysteroscopic Septoplasty

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This case report describes a successful pregnancy and delivery in an 18-year-old woman with Herlyn-Werner-Wunderlich Syndrome who previously underwent hysteroscopic septoplasty.

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⚙ AI-generated deep summary by claude@2026-07, 2026-07-16 · read from full text ⓘ

This case report describes an 18-year-old with Herlyn-Werner-Wunderlich syndrome (a congenital malformation associated with genital tract and urinary abnormalities) who previously underwent hysteroscopic vaginal septoplasty after diagnosis, and later achieved a successful gestation. The pregnancy was complicated by prelabor rupture of ovular membranes and progressed to abdominal delivery after 5 days due to severe preeclampsia, but the delivery and neonatal condition were reported as uncomplicated. The authors discuss that HWWS carriers typically have a didelphys uterus with low obstruction and unilateral renal agenesis, with retained menstrual flow that can lead to infection and a higher risk of endometriosis and infertility, and they state the major limitation is that this is a single case report. The paper explicitly mentions severe endometriosis as a potential consequence of HWWS and infertility, placing it within the endometriosis-relevant corpus context.

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Abstract

Introduction: Herlyn-Werner-Wunderlich Syndrome (HWWS) is an embryological malformation that damages the urinary and genital systems. It may have clinical repercussions as progressive dysmenorrhea and compromise the patient’s obstetric future, with occurrence of severe endometriosis and infertility. Case Report: A patient, 18 years old, admitted for an amniotic fluid loss complaint. She demonstrated a previous diagnosis of HWWS during anamnesis, which was previously discovered and surgically adjusted 4 years earlier, through a hysteroscopic vaginal septoplasty. The patient needed an obstetric admission due to a clinical diagnosis of Prelabor Rupture of Ovular Membranes (PROM), with abdominal delivery after 5 days due to the development of severe preeclampsia. The procedure had no intercurrence, alongside the birth of the conceptus in good clinical conditions. Discussion: The patients who carry that rare syndrome have didelphys uterus, low genital obstruction and unilateral renal agenesis. When the genital obstruction is complete, the symptoms are often more glaring, producing palpable and painful abdominal mass because of the hematocolpos. Regardless of the anatomic space, the retained flow is susceptible to infections and may cause abdominal sepsis. Furthermore, the patient can acquire infertility for the higher risk of endometriosis or for the anatomic distortions. The cirurgical adjustment is associated with good pregnancy rates and should always be suggested to those patients. Conclusion: Considering the serious repercussions to the life quality of those patients, the Herlyn-Werner-Wunderlich Syndrome (HWWS) should always be present in differential diagnosis of a specialist doctor’s routine. The premature diagnosis leads to a necessary adjustment and contributes to positive and favorable results in the reproductive life of such patients.
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Introduction

Herlyn-Werner-Wunderlich Syndrome (HWWS) is an embryological malformation that damages the urinary and genital systems. It may have clinical repercussions as progressive dysmenorrhea and compromise the patient’s obstetric future, with occurrence of severe endometriosis and infertility. Case Report: A patient, 18 years old, admitted for an amniotic fluid loss complaint. She demonstrated a previous diagnosis of HWWS during anamnesis, which was previously discovered and surgically adjusted 4 years earlier, through a hysteroscopic vaginal septoplasty. The patient needed an obstetric admission due to a clinical diagnosis of Prelabor Rupture of Ovular Membranes (PROM), with abdominal delivery after 5 days due to the development of severe preeclampsia. The procedure had no intercurrence, alongside the birth of the conceptus in good clinical conditions.

Discussion

The patients who carry that rare syndrome have didelphys uterus, low genital obstruction and unilateral renal agenesis. When the genital obstruction is complete, the symptoms are often more glaring, producing palpable and painful abdominal mass because of the hematocolpos. Regardless of the anatomic space, the retained flow is susceptible to infections and may cause abdominal sepsis. Furthermore, the patient can acquire infertility for the higher risk of endometriosis or for the anatomic distortions. The cirurgical adjustment is associated with good pregnancy rates and should always be suggested to those patients.

Conclusion

Considering the serious repercussions to the life quality of those patients, the Herlyn-Werner-Wunderlich Syndrome (HWWS) should always be present in differential diagnosis of a specialist doctor’s routine. The premature diagnosis leads to a necessary adjustment and contributes to positive and favorable results in the reproductive life of such patients. Files 2126-Article Text-5609-1-10-20250218.pdf Files (624.3 kB) | Name | Size | Download all | |---|---|---| | md5:36768553f42cc7ea55e6f6b3f64c1c8f | 624.3 kB | Preview Download |

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endometriosisdysmenorrheainfertility

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