{"title":"青少年颞动脉炎伴嗜酸性粒细胞增多综合征,伪装成头皮表皮包皮囊肿","authors":"Maheshri Deshpande, Geet Bhuyan","doi":"10.4103/ijves.ijves_51_22","DOIUrl":null,"url":null,"abstract":"A 34-year-old man came to the outpatient department with subcutaneous nodules in the temporal area. He did not complain of any other symptoms. Computed tomography scan revealed a nodule of 40.5 HU in the temporal region of the scalp. A possibility of an epidermal inclusion cyst was given. The lesion was excised and the biopsy revealed vasculitis with eosinophilia without giant cell formation. A final diagnosis of juvenile temporal arteritis with hypereosinophilic syndrome was given based on the clinical, radiological, and histopathological findings.","PeriodicalId":13375,"journal":{"name":"Indian Journal of Vascular and Endovascular Surgery","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Juvenile temporal arteritis with hypereosinophilic syndrome masquerading as an epidermal inclusion cyst of the scalp\",\"authors\":\"Maheshri Deshpande, Geet Bhuyan\",\"doi\":\"10.4103/ijves.ijves_51_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A 34-year-old man came to the outpatient department with subcutaneous nodules in the temporal area. He did not complain of any other symptoms. Computed tomography scan revealed a nodule of 40.5 HU in the temporal region of the scalp. A possibility of an epidermal inclusion cyst was given. The lesion was excised and the biopsy revealed vasculitis with eosinophilia without giant cell formation. A final diagnosis of juvenile temporal arteritis with hypereosinophilic syndrome was given based on the clinical, radiological, and histopathological findings.\",\"PeriodicalId\":13375,\"journal\":{\"name\":\"Indian Journal of Vascular and Endovascular Surgery\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2023-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Vascular and Endovascular Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ijves.ijves_51_22\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Vascular and Endovascular Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijves.ijves_51_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
Juvenile temporal arteritis with hypereosinophilic syndrome masquerading as an epidermal inclusion cyst of the scalp
A 34-year-old man came to the outpatient department with subcutaneous nodules in the temporal area. He did not complain of any other symptoms. Computed tomography scan revealed a nodule of 40.5 HU in the temporal region of the scalp. A possibility of an epidermal inclusion cyst was given. The lesion was excised and the biopsy revealed vasculitis with eosinophilia without giant cell formation. A final diagnosis of juvenile temporal arteritis with hypereosinophilic syndrome was given based on the clinical, radiological, and histopathological findings.