{"title":"弥散性大疱和不适","authors":"A. Bohne, T. Schwarz, U. Wehkamp","doi":"10.1111/ddg.13938","DOIUrl":null,"url":null,"abstract":"A 52-year-old female patient presented with a history of increasing erythematous and centrally bullous plaques over six days. The patient reported a general feeling of malaise and light-headedness and denied taking any medication during the past eight weeks. She described the lesions as slightly itchy and tender, and did not report a previous infection. A few years ago, the patient experienced a transitory ischemic attack but was otherwise healthy.","PeriodicalId":14702,"journal":{"name":"JDDG: Journal der Deutschen Dermatologischen Gesellschaft","volume":"36 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Disseminated bullae and malaise\",\"authors\":\"A. Bohne, T. Schwarz, U. Wehkamp\",\"doi\":\"10.1111/ddg.13938\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A 52-year-old female patient presented with a history of increasing erythematous and centrally bullous plaques over six days. The patient reported a general feeling of malaise and light-headedness and denied taking any medication during the past eight weeks. She described the lesions as slightly itchy and tender, and did not report a previous infection. A few years ago, the patient experienced a transitory ischemic attack but was otherwise healthy.\",\"PeriodicalId\":14702,\"journal\":{\"name\":\"JDDG: Journal der Deutschen Dermatologischen Gesellschaft\",\"volume\":\"36 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JDDG: Journal der Deutschen Dermatologischen Gesellschaft\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1111/ddg.13938\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JDDG: Journal der Deutschen Dermatologischen Gesellschaft","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/ddg.13938","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A 52-year-old female patient presented with a history of increasing erythematous and centrally bullous plaques over six days. The patient reported a general feeling of malaise and light-headedness and denied taking any medication during the past eight weeks. She described the lesions as slightly itchy and tender, and did not report a previous infection. A few years ago, the patient experienced a transitory ischemic attack but was otherwise healthy.