{"title":"三方视网膜母细胞瘤","authors":"","doi":"10.32388/dpeidi","DOIUrl":null,"url":null,"abstract":"INTRODUCTION Trilateral retinoblastoma (TR) is characterised by an intracranial neuroblastic tumour arising in the pineal region, associated with hereditary retinoblastomas which are usually bilateral but may also be unilateral. TR is rare, occurring in 3% of cases and is usually fatal . From August 2001 till December 2009, a total of 141 cases of retinoblastoma were seen at our institution. During this time, two children progressed to trilateral disease (1.4%).","PeriodicalId":77200,"journal":{"name":"Journal of clinical neuro-ophthalmology","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Trilateral Retinoblastoma\",\"authors\":\"\",\"doi\":\"10.32388/dpeidi\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"INTRODUCTION Trilateral retinoblastoma (TR) is characterised by an intracranial neuroblastic tumour arising in the pineal region, associated with hereditary retinoblastomas which are usually bilateral but may also be unilateral. TR is rare, occurring in 3% of cases and is usually fatal . From August 2001 till December 2009, a total of 141 cases of retinoblastoma were seen at our institution. During this time, two children progressed to trilateral disease (1.4%).\",\"PeriodicalId\":77200,\"journal\":{\"name\":\"Journal of clinical neuro-ophthalmology\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical neuro-ophthalmology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/dpeidi\",\"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 clinical neuro-ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/dpeidi","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
INTRODUCTION Trilateral retinoblastoma (TR) is characterised by an intracranial neuroblastic tumour arising in the pineal region, associated with hereditary retinoblastomas which are usually bilateral but may also be unilateral. TR is rare, occurring in 3% of cases and is usually fatal . From August 2001 till December 2009, a total of 141 cases of retinoblastoma were seen at our institution. During this time, two children progressed to trilateral disease (1.4%).
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