{"title":"嗜血细胞淋巴组织细胞增多症中的塌陷性肾小球病变","authors":"Figer Ishika R, Shinde Sweety V","doi":"10.36106/gjra/1405345","DOIUrl":null,"url":null,"abstract":"Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinammatory syndrome due to abnormal immune process and multiorgan inltration by phagocytic histiocytes. Renal presentation is very rare. Collapsing glomerulopathy with underlying autoimmune disease leading to HLH is documented in the present case.","PeriodicalId":12664,"journal":{"name":"Global journal for research analysis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"COLLAPSING GLOMERULOPATHY IN HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS\",\"authors\":\"Figer Ishika R, Shinde Sweety V\",\"doi\":\"10.36106/gjra/1405345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinammatory syndrome due to abnormal immune process and multiorgan inltration by phagocytic histiocytes. Renal presentation is very rare. Collapsing glomerulopathy with underlying autoimmune disease leading to HLH is documented in the present case.\",\"PeriodicalId\":12664,\"journal\":{\"name\":\"Global journal for research analysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Global journal for research analysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36106/gjra/1405345\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global journal for research analysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/gjra/1405345","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
COLLAPSING GLOMERULOPATHY IN HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinammatory syndrome due to abnormal immune process and multiorgan inltration by phagocytic histiocytes. Renal presentation is very rare. Collapsing glomerulopathy with underlying autoimmune disease leading to HLH is documented in the present case.
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