{"title":"Lhermitte-Duclos病是考登综合征的一个组成部分:典型的MRI表现","authors":" . F, Z. K, Gakosso C, B. B, O. M, C. N","doi":"10.36349/easjrit.2021.v03i02.009","DOIUrl":null,"url":null,"abstract":"Quick Response Code Abstract: Lhermitte-Duclos disease or dysplastic cerebellar gangliocytoma is a rare entity characterized by a hamartomatous lesion in the posterior fossa. Cowden’s syndrome or hamartoma-neoplasia syndrome is a rare underdiagnosed autosomal dominant genodermatosis with high incidence of malignant tumors. Lhermitte-Duclos disease may be a component of Cowden’s syndrome.","PeriodicalId":429686,"journal":{"name":"EAS Journal of Radiology and Imaging Technology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lhermitte-Duclos Disease is a Component of Cowden Syndrome: Typical MRI Findings\",\"authors\":\" . F, Z. K, Gakosso C, B. B, O. M, C. N\",\"doi\":\"10.36349/easjrit.2021.v03i02.009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Quick Response Code Abstract: Lhermitte-Duclos disease or dysplastic cerebellar gangliocytoma is a rare entity characterized by a hamartomatous lesion in the posterior fossa. Cowden’s syndrome or hamartoma-neoplasia syndrome is a rare underdiagnosed autosomal dominant genodermatosis with high incidence of malignant tumors. Lhermitte-Duclos disease may be a component of Cowden’s syndrome.\",\"PeriodicalId\":429686,\"journal\":{\"name\":\"EAS Journal of Radiology and Imaging Technology\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EAS Journal of Radiology and Imaging Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36349/easjrit.2021.v03i02.009\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EAS Journal of Radiology and Imaging Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36349/easjrit.2021.v03i02.009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Lhermitte-Duclos Disease is a Component of Cowden Syndrome: Typical MRI Findings
Quick Response Code Abstract: Lhermitte-Duclos disease or dysplastic cerebellar gangliocytoma is a rare entity characterized by a hamartomatous lesion in the posterior fossa. Cowden’s syndrome or hamartoma-neoplasia syndrome is a rare underdiagnosed autosomal dominant genodermatosis with high incidence of malignant tumors. Lhermitte-Duclos disease may be a component of Cowden’s syndrome.
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