Supriya S Shinde, Jagadish Chinnappa, B. Shenoy, Tripti Kaur Sagar Bhattad
{"title":"跳出框框思考!儿童发病成人结节病在一个年幼的孩子表现为不明原因的发热","authors":"Supriya S Shinde, Jagadish Chinnappa, B. Shenoy, Tripti Kaur Sagar Bhattad","doi":"10.37532/1758-4272.2020.15(5).131-132","DOIUrl":null,"url":null,"abstract":"Sarcoidosis is a rare multi-systemic granulomatous disease that can have myriad of presentations in childhood. A five-year old female child presented with recurrent fever from two years of age and hepato-splenomegaly. She had no arthritis, rash or uveitis. She had been extensively investigated and yet, remained undiagnosed for a period of three years. Finally, a liver and lymph node biopsy yielded the diagnosis of sarcoidosis. In children presenting with pyrexia of unknown origin (PUO), when a thorough history, physical examination and initial investigations fail to provide direction, tissue biopsy must be considered. To the best of our knowledge, this is the first report of pediatric-onset adult sarcoidosis presenting at such a young age, from the Indian subcontinent. It aptly high-lights the need to consider sarcoidosis as a possibility in children presenting with PUO.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"33 1","pages":"131"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Think out of the box! Pediatric onset adult Sarcoidosis in a young child presenting as Pyrexia of unknown origin\",\"authors\":\"Supriya S Shinde, Jagadish Chinnappa, B. Shenoy, Tripti Kaur Sagar Bhattad\",\"doi\":\"10.37532/1758-4272.2020.15(5).131-132\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sarcoidosis is a rare multi-systemic granulomatous disease that can have myriad of presentations in childhood. A five-year old female child presented with recurrent fever from two years of age and hepato-splenomegaly. She had no arthritis, rash or uveitis. She had been extensively investigated and yet, remained undiagnosed for a period of three years. Finally, a liver and lymph node biopsy yielded the diagnosis of sarcoidosis. In children presenting with pyrexia of unknown origin (PUO), when a thorough history, physical examination and initial investigations fail to provide direction, tissue biopsy must be considered. To the best of our knowledge, this is the first report of pediatric-onset adult sarcoidosis presenting at such a young age, from the Indian subcontinent. It aptly high-lights the need to consider sarcoidosis as a possibility in children presenting with PUO.\",\"PeriodicalId\":13740,\"journal\":{\"name\":\"International Journal of Clinical Rheumatology\",\"volume\":\"33 1\",\"pages\":\"131\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Clinical Rheumatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37532/1758-4272.2020.15(5).131-132\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37532/1758-4272.2020.15(5).131-132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Think out of the box! Pediatric onset adult Sarcoidosis in a young child presenting as Pyrexia of unknown origin
Sarcoidosis is a rare multi-systemic granulomatous disease that can have myriad of presentations in childhood. A five-year old female child presented with recurrent fever from two years of age and hepato-splenomegaly. She had no arthritis, rash or uveitis. She had been extensively investigated and yet, remained undiagnosed for a period of three years. Finally, a liver and lymph node biopsy yielded the diagnosis of sarcoidosis. In children presenting with pyrexia of unknown origin (PUO), when a thorough history, physical examination and initial investigations fail to provide direction, tissue biopsy must be considered. To the best of our knowledge, this is the first report of pediatric-onset adult sarcoidosis presenting at such a young age, from the Indian subcontinent. It aptly high-lights the need to consider sarcoidosis as a possibility in children presenting with PUO.