{"title":"儿童脑白质病伴广泛脑钙化和实质囊肿","authors":"Sanaa El Mouhadi, Latifa Chat, Rachida Dafiri","doi":"10.1016/j.ejrex.2011.04.009","DOIUrl":null,"url":null,"abstract":"<div><p>Leukoencephalopathy<span> with cerebral calcifications and cysts (LCC) is a recently described and extremely rare entity of unknown origin characterized radiologically by white matter abnormalities, calcifications and cysts. The onset of this disorder occurs from early infancy to adolescence and there is no specific clinical feature suggestive of this disorder. We report a new case of this rare entity and emphasize CT and MRI findings that permit to assess diagnosis.</span></p></div>","PeriodicalId":100506,"journal":{"name":"European Journal of Radiology Extra","volume":"79 2","pages":"Pages e85-e88"},"PeriodicalIF":0.0000,"publicationDate":"2011-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ejrex.2011.04.009","citationCount":"3","resultStr":"{\"title\":\"Leukoencephalopathy with extensive brain calcifications and parenchymal cysts in a child\",\"authors\":\"Sanaa El Mouhadi, Latifa Chat, Rachida Dafiri\",\"doi\":\"10.1016/j.ejrex.2011.04.009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Leukoencephalopathy<span> with cerebral calcifications and cysts (LCC) is a recently described and extremely rare entity of unknown origin characterized radiologically by white matter abnormalities, calcifications and cysts. The onset of this disorder occurs from early infancy to adolescence and there is no specific clinical feature suggestive of this disorder. We report a new case of this rare entity and emphasize CT and MRI findings that permit to assess diagnosis.</span></p></div>\",\"PeriodicalId\":100506,\"journal\":{\"name\":\"European Journal of Radiology Extra\",\"volume\":\"79 2\",\"pages\":\"Pages e85-e88\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.ejrex.2011.04.009\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Radiology Extra\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1571467511000587\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Radiology Extra","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1571467511000587","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Leukoencephalopathy with extensive brain calcifications and parenchymal cysts in a child
Leukoencephalopathy with cerebral calcifications and cysts (LCC) is a recently described and extremely rare entity of unknown origin characterized radiologically by white matter abnormalities, calcifications and cysts. The onset of this disorder occurs from early infancy to adolescence and there is no specific clinical feature suggestive of this disorder. We report a new case of this rare entity and emphasize CT and MRI findings that permit to assess diagnosis.