{"title":"melkersson–Rosenthal综合征伴双侧颞视盘苍白的完整临床谱——一例报告","authors":"Henal Javeri, Dipankar Das, Shahinur Tayab, Gayatri Bharali, H. Bhattacharjee, Suklengmung Buragohain","doi":"10.4103/tjosr.tjosr_134_20","DOIUrl":null,"url":null,"abstract":"Melkersson Rosenthal syndrome (MRS) is a very rare neuro-mucocutaneous disease, the aetiology of which is not well defined. It is classically characterised by recurring facial paralysis, swelling of face, lips and presence of a furrowed tongue. The presentation is usually oligosymtomatic, with only about one-fourth of cases showing the classical triad. Here, we present a 32-year-old female with MRS, showing the complete clinical triad of symptoms. We report for the first time, an association of MRS with bilateral optic nerve involvement. A standard criterion for diagnosis and management is lacking. It is important to increase awareness of such a rare syndrome with various associated manifestations, so that it can be accurately identified and treated.","PeriodicalId":34180,"journal":{"name":"TNOA Journal of Ophthalmic Science and Research","volume":"61 1","pages":"123 - 125"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Complete clinical spectrum of melkersson–Rosenthal syndrome with bilateral temporal optic disc pallor – A case report\",\"authors\":\"Henal Javeri, Dipankar Das, Shahinur Tayab, Gayatri Bharali, H. Bhattacharjee, Suklengmung Buragohain\",\"doi\":\"10.4103/tjosr.tjosr_134_20\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Melkersson Rosenthal syndrome (MRS) is a very rare neuro-mucocutaneous disease, the aetiology of which is not well defined. It is classically characterised by recurring facial paralysis, swelling of face, lips and presence of a furrowed tongue. The presentation is usually oligosymtomatic, with only about one-fourth of cases showing the classical triad. Here, we present a 32-year-old female with MRS, showing the complete clinical triad of symptoms. We report for the first time, an association of MRS with bilateral optic nerve involvement. A standard criterion for diagnosis and management is lacking. It is important to increase awareness of such a rare syndrome with various associated manifestations, so that it can be accurately identified and treated.\",\"PeriodicalId\":34180,\"journal\":{\"name\":\"TNOA Journal of Ophthalmic Science and Research\",\"volume\":\"61 1\",\"pages\":\"123 - 125\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"TNOA Journal of Ophthalmic Science and Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/tjosr.tjosr_134_20\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"TNOA Journal of Ophthalmic Science and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/tjosr.tjosr_134_20","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Complete clinical spectrum of melkersson–Rosenthal syndrome with bilateral temporal optic disc pallor – A case report
Melkersson Rosenthal syndrome (MRS) is a very rare neuro-mucocutaneous disease, the aetiology of which is not well defined. It is classically characterised by recurring facial paralysis, swelling of face, lips and presence of a furrowed tongue. The presentation is usually oligosymtomatic, with only about one-fourth of cases showing the classical triad. Here, we present a 32-year-old female with MRS, showing the complete clinical triad of symptoms. We report for the first time, an association of MRS with bilateral optic nerve involvement. A standard criterion for diagnosis and management is lacking. It is important to increase awareness of such a rare syndrome with various associated manifestations, so that it can be accurately identified and treated.