Background. The Herlyn-Werner-Wunderlich syndrome (HWWS) is an un-common congenital anomaly, characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. We report a unique case of association of HWWS and central placenta previa (CPP) in a COVID-19-positive pregnant woman. Case presentation. A 39-year-old pregnant woman was admitted to our hospital for preterm labour risk at 32 gestational weeks. She referred a previous caesarean section (CS) and three miscarriages. Speculum examination allowed visualization of the left cervix, whereas the contralateral one was hidden under the obliterated vaginal septum. Ultrasound examination showed poste-ro-lateral CPP, double uterus, and right renal agenesis. Subsequent Magnetic Resonance Imaging confirmed the condition of uterus didelphys and right renal agenesis, associated with CPP. The patient was treated with tocolytics and progesterone and was discharged in good physical condition. At 35 gestation-al weeks, the patient became COVID-19-positive with few symptoms. Elective CS was performed at 36 gestational weeks, and she delivered a small-for-ges-tational-age newborn in good health conditions. The left womb was partic-ularly bleeding on the lower uterine segment and ligation of the left uterine artery was necessary. The postoperative course was uneventful. Conclusions. We describe a unique association of HWWS and CPP in a COVID-19-positive pregnant woman solved by means of elective CS and uterine artery ligation. Pregnancy in women with HWWS is possible, although obstetric complications may arise. When HWWS is associated with CPP, the risk of haemorrhage is the rule. A correct management determined positive both maternal and foetal outcomes

Herlyn-Werner-Wunderlich syndrome and central placenta previa in a COVID-19 positive pregnant woman: a case report

Vito Leanza;Marianna Gulisano;Sonia Graziella Correnti;Marco Palumbo
2023-01-01

Abstract

Background. The Herlyn-Werner-Wunderlich syndrome (HWWS) is an un-common congenital anomaly, characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. We report a unique case of association of HWWS and central placenta previa (CPP) in a COVID-19-positive pregnant woman. Case presentation. A 39-year-old pregnant woman was admitted to our hospital for preterm labour risk at 32 gestational weeks. She referred a previous caesarean section (CS) and three miscarriages. Speculum examination allowed visualization of the left cervix, whereas the contralateral one was hidden under the obliterated vaginal septum. Ultrasound examination showed poste-ro-lateral CPP, double uterus, and right renal agenesis. Subsequent Magnetic Resonance Imaging confirmed the condition of uterus didelphys and right renal agenesis, associated with CPP. The patient was treated with tocolytics and progesterone and was discharged in good physical condition. At 35 gestation-al weeks, the patient became COVID-19-positive with few symptoms. Elective CS was performed at 36 gestational weeks, and she delivered a small-for-ges-tational-age newborn in good health conditions. The left womb was partic-ularly bleeding on the lower uterine segment and ligation of the left uterine artery was necessary. The postoperative course was uneventful. Conclusions. We describe a unique association of HWWS and CPP in a COVID-19-positive pregnant woman solved by means of elective CS and uterine artery ligation. Pregnancy in women with HWWS is possible, although obstetric complications may arise. When HWWS is associated with CPP, the risk of haemorrhage is the rule. A correct management determined positive both maternal and foetal outcomes
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/647384
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