{"title":"胎儿IV型肝内门静脉分流的产前超声诊断:1例罕见报告。","authors":"Zixian Wei, Wenle Zhang, Zhibin Tan, Sufen Zhou","doi":"10.1002/jcu.23994","DOIUrl":null,"url":null,"abstract":"<p><p>Fetal intrahepatic portosystemic shunt (IPSS) is a rare vascular anomaly that poses significant postnatal risks. Paul et al. classified congenital IPSS into four types: (I) a single large tube connecting the right portal vein to the inferior vena cava; (II) a localized peripheral shunt with communications in one hepatic segment; (III) an aneurysmal shunt; (IV) multiple diffuse communications in both lobes. We report a unique case of Type IV IPSS diagnosed at 29 weeks of gestation using prenatal ultrasound and Doppler imaging. The shunt was characterized by tortuous portal vein branches draining into hepatic veins, accompanied by fetal growth restriction and mild tricuspid regurgitation. This case highlights the value of detailed prenatal imaging for accurate diagnosis, classification, and perinatal planning. Early identification and close monitoring of fetal IPSS can optimize neonatal outcomes and guide postnatal interventions.</p>","PeriodicalId":15386,"journal":{"name":"Journal of Clinical Ultrasound","volume":" ","pages":""},"PeriodicalIF":1.2000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prenatal Ultrasound Diagnosis of Fetal Type IV Intrahepatic Portosystemic Shunt: A Rare Case Report.\",\"authors\":\"Zixian Wei, Wenle Zhang, Zhibin Tan, Sufen Zhou\",\"doi\":\"10.1002/jcu.23994\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fetal intrahepatic portosystemic shunt (IPSS) is a rare vascular anomaly that poses significant postnatal risks. Paul et al. classified congenital IPSS into four types: (I) a single large tube connecting the right portal vein to the inferior vena cava; (II) a localized peripheral shunt with communications in one hepatic segment; (III) an aneurysmal shunt; (IV) multiple diffuse communications in both lobes. We report a unique case of Type IV IPSS diagnosed at 29 weeks of gestation using prenatal ultrasound and Doppler imaging. The shunt was characterized by tortuous portal vein branches draining into hepatic veins, accompanied by fetal growth restriction and mild tricuspid regurgitation. This case highlights the value of detailed prenatal imaging for accurate diagnosis, classification, and perinatal planning. Early identification and close monitoring of fetal IPSS can optimize neonatal outcomes and guide postnatal interventions.</p>\",\"PeriodicalId\":15386,\"journal\":{\"name\":\"Journal of Clinical Ultrasound\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2025-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Ultrasound\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/jcu.23994\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ACOUSTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Ultrasound","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jcu.23994","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ACOUSTICS","Score":null,"Total":0}
Prenatal Ultrasound Diagnosis of Fetal Type IV Intrahepatic Portosystemic Shunt: A Rare Case Report.
Fetal intrahepatic portosystemic shunt (IPSS) is a rare vascular anomaly that poses significant postnatal risks. Paul et al. classified congenital IPSS into four types: (I) a single large tube connecting the right portal vein to the inferior vena cava; (II) a localized peripheral shunt with communications in one hepatic segment; (III) an aneurysmal shunt; (IV) multiple diffuse communications in both lobes. We report a unique case of Type IV IPSS diagnosed at 29 weeks of gestation using prenatal ultrasound and Doppler imaging. The shunt was characterized by tortuous portal vein branches draining into hepatic veins, accompanied by fetal growth restriction and mild tricuspid regurgitation. This case highlights the value of detailed prenatal imaging for accurate diagnosis, classification, and perinatal planning. Early identification and close monitoring of fetal IPSS can optimize neonatal outcomes and guide postnatal interventions.
期刊介绍:
The Journal of Clinical Ultrasound (JCU) is an international journal dedicated to the worldwide dissemination of scientific information on diagnostic and therapeutic applications of medical sonography.
The scope of the journal includes--but is not limited to--the following areas: sonography of the gastrointestinal tract, genitourinary tract, vascular system, nervous system, head and neck, chest, breast, musculoskeletal system, and other superficial structures; Doppler applications; obstetric and pediatric applications; and interventional sonography. Studies comparing sonography with other imaging modalities are encouraged, as are studies evaluating the economic impact of sonography. Also within the journal''s scope are innovations and improvements in instrumentation and examination techniques and the use of contrast agents.
JCU publishes original research articles, case reports, pictorial essays, technical notes, and letters to the editor. The journal is also dedicated to being an educational resource for its readers, through the publication of review articles and various scientific contributions from members of the editorial board and other world-renowned experts in sonography.