Helena C. Bartels, Greg Ryan, Edgar Jaeggi, Homero Flores-Mendoza
{"title":"Maternal-fetal complications of non-immune fetal hydrops – mirror syndrome and hypereactio luteinalis with ovarian torsion: A case report","authors":"Helena C. Bartels, Greg Ryan, Edgar Jaeggi, Homero Flores-Mendoza","doi":"10.1016/j.crwh.2025.e00775","DOIUrl":null,"url":null,"abstract":"<div><div>Mirror syndrome, previously referred to as Ballantyne's syndrome, is a rare obstetric disorder characterized by maternal edema in association with fetal hydrops and placental edema. This report concerns the case of a 35-year-old multiparous woman who developed mirror syndrome secondary to fetal supraventricular tachycardia complicated by hydrops and intrauterine fetal demise. Her pregnancy was further complicated by hypereactio luteinalis with ovarian torsion requiring surgical detorsion. The case highlights the challenges of managing maternal and fetal hydrps, and its rare association with hypereactio luteinalis.</div></div>","PeriodicalId":9657,"journal":{"name":"Case Reports in Women's Health","volume":"49 ","pages":"Article e00775"},"PeriodicalIF":0.6000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Women's Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214911225000967","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/12 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mirror syndrome, previously referred to as Ballantyne's syndrome, is a rare obstetric disorder characterized by maternal edema in association with fetal hydrops and placental edema. This report concerns the case of a 35-year-old multiparous woman who developed mirror syndrome secondary to fetal supraventricular tachycardia complicated by hydrops and intrauterine fetal demise. Her pregnancy was further complicated by hypereactio luteinalis with ovarian torsion requiring surgical detorsion. The case highlights the challenges of managing maternal and fetal hydrps, and its rare association with hypereactio luteinalis.