{"title":"作为嗜酸性筋膜炎线索的凹槽征象","authors":"Niharikaa J, Yogindher Singh R","doi":"10.52403/ijhsr.20240723","DOIUrl":null,"url":null,"abstract":"Eosinophilic fasciitis is a rare variant of scleroderma with an unknown etiology, predominantly affecting middle age group. Clinically it presents with local oedema, erythema, woody induration with an “orange peel” appearance, progressing rapidly to fibrosis associated with hematological changes mainly eosinophilia. A deep fascial biopsy and imaging studies aid the diagnosis. Classical skin findings help in early diagnosis thereby preserving the mobility and preventing the joint contractures. This report presents a case of 59-year-old male with features suggestive of eosinophilic fasciitis and its importance in diagnosis.\n\nKey words: Groove sign, peau d’ orange appearance, dermascopy, Eosinophilic fasciitis, Shulman syndrome.","PeriodicalId":14119,"journal":{"name":"International Journal of Health Sciences and Research","volume":"78 18","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Groove Sign as an Eosinophilic Fasciitis Clue\",\"authors\":\"Niharikaa J, Yogindher Singh R\",\"doi\":\"10.52403/ijhsr.20240723\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Eosinophilic fasciitis is a rare variant of scleroderma with an unknown etiology, predominantly affecting middle age group. Clinically it presents with local oedema, erythema, woody induration with an “orange peel” appearance, progressing rapidly to fibrosis associated with hematological changes mainly eosinophilia. A deep fascial biopsy and imaging studies aid the diagnosis. Classical skin findings help in early diagnosis thereby preserving the mobility and preventing the joint contractures. This report presents a case of 59-year-old male with features suggestive of eosinophilic fasciitis and its importance in diagnosis.\\n\\nKey words: Groove sign, peau d’ orange appearance, dermascopy, Eosinophilic fasciitis, Shulman syndrome.\",\"PeriodicalId\":14119,\"journal\":{\"name\":\"International Journal of Health Sciences and Research\",\"volume\":\"78 18\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Health Sciences and Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.52403/ijhsr.20240723\",\"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 Health Sciences and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52403/ijhsr.20240723","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Eosinophilic fasciitis is a rare variant of scleroderma with an unknown etiology, predominantly affecting middle age group. Clinically it presents with local oedema, erythema, woody induration with an “orange peel” appearance, progressing rapidly to fibrosis associated with hematological changes mainly eosinophilia. A deep fascial biopsy and imaging studies aid the diagnosis. Classical skin findings help in early diagnosis thereby preserving the mobility and preventing the joint contractures. This report presents a case of 59-year-old male with features suggestive of eosinophilic fasciitis and its importance in diagnosis.
Key words: Groove sign, peau d’ orange appearance, dermascopy, Eosinophilic fasciitis, Shulman syndrome.