Robert J. Purgert, Jose J. Echegaray, S. Lauer, Arun D. Singh
{"title":"后天性脉络膜骨瘤","authors":"Robert J. Purgert, Jose J. Echegaray, S. Lauer, Arun D. Singh","doi":"10.25259/LAJO-3-2019","DOIUrl":null,"url":null,"abstract":"Choroidal osteoma is a choristomatous lesion postulated to be congenital in nature. Described herein is the case of a 16-year- old female presenting with a peripapillary lesion diagnosed as choroidal osteoma on multimodal imaging. Routine fundus photography 18 months before presentation demonstrated a normal retina and choroid without evidence of the lesion. Overall, this report provides evidence that choroidal osteoma may be acquired and not always congenital in origin.","PeriodicalId":437914,"journal":{"name":"Latin American Journal of Ophthalmology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Acquired choroidal osteoma\",\"authors\":\"Robert J. Purgert, Jose J. Echegaray, S. Lauer, Arun D. Singh\",\"doi\":\"10.25259/LAJO-3-2019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Choroidal osteoma is a choristomatous lesion postulated to be congenital in nature. Described herein is the case of a 16-year- old female presenting with a peripapillary lesion diagnosed as choroidal osteoma on multimodal imaging. Routine fundus photography 18 months before presentation demonstrated a normal retina and choroid without evidence of the lesion. Overall, this report provides evidence that choroidal osteoma may be acquired and not always congenital in origin.\",\"PeriodicalId\":437914,\"journal\":{\"name\":\"Latin American Journal of Ophthalmology\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Latin American Journal of Ophthalmology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25259/LAJO-3-2019\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Latin American Journal of Ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/LAJO-3-2019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Choroidal osteoma is a choristomatous lesion postulated to be congenital in nature. Described herein is the case of a 16-year- old female presenting with a peripapillary lesion diagnosed as choroidal osteoma on multimodal imaging. Routine fundus photography 18 months before presentation demonstrated a normal retina and choroid without evidence of the lesion. Overall, this report provides evidence that choroidal osteoma may be acquired and not always congenital in origin.
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