{"title":"涉及免疫球蛋白g4相关硬化疾病患者皮肤的异时性多重临床表现","authors":"Wei-Feng Huang, Yi-Ping Chen, Wei Liu","doi":"10.51941/amcr.2022.2107","DOIUrl":null,"url":null,"abstract":"years after resection without recognition of IgG4-RD. As the primary skin lesion prior to the systemic symptoms was rare and mostly appeared in head and neck (Charrow et al ., 2016). Once again at this recurrence, cutaneous dermatofibroma wasn’t initially identified as the primary symptom of IgG4 -RD. Therefore, IgG4-RD should be fully considered and evaluated in clinical practices to avoid unnecessary and potentially harmful operations.","PeriodicalId":310782,"journal":{"name":"Archives of Medical and Clinical Research","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metachronous Multiple Clinical Presentations Involving the Skin in a Patient with Immunoglobulin G4–Related Sclerosing Disease\",\"authors\":\"Wei-Feng Huang, Yi-Ping Chen, Wei Liu\",\"doi\":\"10.51941/amcr.2022.2107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"years after resection without recognition of IgG4-RD. As the primary skin lesion prior to the systemic symptoms was rare and mostly appeared in head and neck (Charrow et al ., 2016). Once again at this recurrence, cutaneous dermatofibroma wasn’t initially identified as the primary symptom of IgG4 -RD. Therefore, IgG4-RD should be fully considered and evaluated in clinical practices to avoid unnecessary and potentially harmful operations.\",\"PeriodicalId\":310782,\"journal\":{\"name\":\"Archives of Medical and Clinical Research\",\"volume\":\"23 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Medical and Clinical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.51941/amcr.2022.2107\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Medical and Clinical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51941/amcr.2022.2107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
术后数年未发现IgG4-RD。由于全身性症状出现之前的原发性皮肤病变很少，且多出现在头颈部(Charrow et al .， 2016)。同样，在复发时，皮肤皮肤纤维瘤最初并未被确定为IgG4 -RD的主要症状。因此，在临床实践中应充分考虑和评估IgG4-RD，以避免不必要和潜在有害的手术。
Metachronous Multiple Clinical Presentations Involving the Skin in a Patient with Immunoglobulin G4–Related Sclerosing Disease
years after resection without recognition of IgG4-RD. As the primary skin lesion prior to the systemic symptoms was rare and mostly appeared in head and neck (Charrow et al ., 2016). Once again at this recurrence, cutaneous dermatofibroma wasn’t initially identified as the primary symptom of IgG4 -RD. Therefore, IgG4-RD should be fully considered and evaluated in clinical practices to avoid unnecessary and potentially harmful operations.
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