{"title":"自发性颅内低血压表现为腰椎假性蛛网膜炎相关的奇亚里畸形和脑积水","authors":"Carter Lacey M, Gross Naina L","doi":"10.36959/595/420","DOIUrl":null,"url":null,"abstract":"Spontaneous intracranial hypotension (SIH) is a rare occurrence, especially in children. In the pediatric population, three cases of Chiari malformation in children and no cases of hydrocephalus due to SIH have been discussed in the literature. We present two patients under the age of five who presented with imaging concerning for the need for neurosurgical intervention later found to be due to SIH that resolved spontaneously.","PeriodicalId":432995,"journal":{"name":"Journal of Pediatric Neurology and Neuroscience","volume":"25 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spontaneous Intracranial Hypotension Presenting with Chiari Malformation and Hydrocephalus Associated With Lumbar Pseudoarachnoiditis\",\"authors\":\"Carter Lacey M, Gross Naina L\",\"doi\":\"10.36959/595/420\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Spontaneous intracranial hypotension (SIH) is a rare occurrence, especially in children. In the pediatric population, three cases of Chiari malformation in children and no cases of hydrocephalus due to SIH have been discussed in the literature. We present two patients under the age of five who presented with imaging concerning for the need for neurosurgical intervention later found to be due to SIH that resolved spontaneously.\",\"PeriodicalId\":432995,\"journal\":{\"name\":\"Journal of Pediatric Neurology and Neuroscience\",\"volume\":\"25 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pediatric Neurology and Neuroscience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36959/595/420\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Neurology and Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36959/595/420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Spontaneous Intracranial Hypotension Presenting with Chiari Malformation and Hydrocephalus Associated With Lumbar Pseudoarachnoiditis
Spontaneous intracranial hypotension (SIH) is a rare occurrence, especially in children. In the pediatric population, three cases of Chiari malformation in children and no cases of hydrocephalus due to SIH have been discussed in the literature. We present two patients under the age of five who presented with imaging concerning for the need for neurosurgical intervention later found to be due to SIH that resolved spontaneously.