{"title":"创伤引起的偶然胎膜积水:跨学科连续性护理","authors":"Jonathan W. Meadows, S. F. Brown","doi":"10.15761/CCSR.1000161","DOIUrl":null,"url":null,"abstract":"Background: Non-immune hydrops fetalis due to Turner syndrome is characterized by hydrops fetalis, cystic hygroma, ascites and eventual fetal demise in most cases. Case: We report on a patient with incidental non-immune hydrops fetalis due to Turner syndrome presenting with hydrops fetalis and ascites on ultrasound, a rare en-caul vaginal delivery, and cystic hygroma, confirmed by cell-free DNA chromosomal analysis. Conclusion: This rare case illustrates the adaptive patient management and interdisplinary coordination of care.","PeriodicalId":10345,"journal":{"name":"Clinical Case Studies and Reports","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Incidental en-caul hydrops fetalis due to trauma: Interdisciplinary continuity of care\",\"authors\":\"Jonathan W. Meadows, S. F. Brown\",\"doi\":\"10.15761/CCSR.1000161\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Non-immune hydrops fetalis due to Turner syndrome is characterized by hydrops fetalis, cystic hygroma, ascites and eventual fetal demise in most cases. Case: We report on a patient with incidental non-immune hydrops fetalis due to Turner syndrome presenting with hydrops fetalis and ascites on ultrasound, a rare en-caul vaginal delivery, and cystic hygroma, confirmed by cell-free DNA chromosomal analysis. Conclusion: This rare case illustrates the adaptive patient management and interdisplinary coordination of care.\",\"PeriodicalId\":10345,\"journal\":{\"name\":\"Clinical Case Studies and Reports\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Case Studies and Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/CCSR.1000161\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Case Studies and Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/CCSR.1000161","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Incidental en-caul hydrops fetalis due to trauma: Interdisciplinary continuity of care
Background: Non-immune hydrops fetalis due to Turner syndrome is characterized by hydrops fetalis, cystic hygroma, ascites and eventual fetal demise in most cases. Case: We report on a patient with incidental non-immune hydrops fetalis due to Turner syndrome presenting with hydrops fetalis and ascites on ultrasound, a rare en-caul vaginal delivery, and cystic hygroma, confirmed by cell-free DNA chromosomal analysis. Conclusion: This rare case illustrates the adaptive patient management and interdisplinary coordination of care.