Sandhya Chauhan, Anchana Gulati, G. Tegta, M. Gupta
{"title":"全身性爆发性组织细胞增多症诊断的临床病理相关性","authors":"Sandhya Chauhan, Anchana Gulati, G. Tegta, M. Gupta","doi":"10.4103/ijdpdd.ijdpdd_44_18","DOIUrl":null,"url":null,"abstract":"Sir, Histiocytoses are a rare group of disorders resulting from reactive or malignant proliferation of mononuclear phagocyte and immunoregulatory effector system. Generalized eruptive histiocytosis (GEH) is a rare variant of histiocytosis first described by Winkelmann and Muller.[1] There are only approximately 43 case reports of GEH till date.[2] We are reporting a 41-year-old male who was suspected as Hansen’s disease, but clinicopathological correlation confirmed GEH.","PeriodicalId":423971,"journal":{"name":"Indian Journal of Dermatopathology and Diagnostic Dermatology","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinicopathological correlation in diagnosis of generalized eruptive histiocytosis\",\"authors\":\"Sandhya Chauhan, Anchana Gulati, G. Tegta, M. Gupta\",\"doi\":\"10.4103/ijdpdd.ijdpdd_44_18\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sir, Histiocytoses are a rare group of disorders resulting from reactive or malignant proliferation of mononuclear phagocyte and immunoregulatory effector system. Generalized eruptive histiocytosis (GEH) is a rare variant of histiocytosis first described by Winkelmann and Muller.[1] There are only approximately 43 case reports of GEH till date.[2] We are reporting a 41-year-old male who was suspected as Hansen’s disease, but clinicopathological correlation confirmed GEH.\",\"PeriodicalId\":423971,\"journal\":{\"name\":\"Indian Journal of Dermatopathology and Diagnostic Dermatology\",\"volume\":\"45 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Dermatopathology and Diagnostic Dermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ijdpdd.ijdpdd_44_18\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Dermatopathology and Diagnostic Dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijdpdd.ijdpdd_44_18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Clinicopathological correlation in diagnosis of generalized eruptive histiocytosis
Sir, Histiocytoses are a rare group of disorders resulting from reactive or malignant proliferation of mononuclear phagocyte and immunoregulatory effector system. Generalized eruptive histiocytosis (GEH) is a rare variant of histiocytosis first described by Winkelmann and Muller.[1] There are only approximately 43 case reports of GEH till date.[2] We are reporting a 41-year-old male who was suspected as Hansen’s disease, but clinicopathological correlation confirmed GEH.