{"title":"SyringocystadenomaPapilliferum Arising from Nevus Sebaceous: A Case Report","authors":"T. Eslammanesh","doi":"10.52547/ajcm.27.4.261","DOIUrl":null,"url":null,"abstract":"Background: Nevus sebaceous is a cutaneous hamartoma accompanied by secondary tumors, such as syringocystadenoma papilliferum. Syringocystadenoma papilliferum is a rare benign tumor with a controversial differentiation between eccrine and apocrine. Most syringocystadenoma papilliferum involving the scalp arises from a nevus sebaceous. Case Presentation: Herein, we report a 15-year-old adolescent female with a congenital skin lesion on the forehead undergoing surgical excision after changing in size and shape of the lesion. After surgical excision and histopathological examination, a diagnosis of syringocystadenoma papilliferum arising from a sebaceous mole was made. Conclusion: Syringocystadenoma papilliferum is a rare skin tumor. Histological confirmation was required for a definitive diagnosis. Furthermore, surgery and complete removal of the lesion are needed for treatment.","PeriodicalId":52678,"journal":{"name":"pzshkhy blyny bn syn","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"pzshkhy blyny bn syn","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52547/ajcm.27.4.261","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Nevus sebaceous is a cutaneous hamartoma accompanied by secondary tumors, such as syringocystadenoma papilliferum. Syringocystadenoma papilliferum is a rare benign tumor with a controversial differentiation between eccrine and apocrine. Most syringocystadenoma papilliferum involving the scalp arises from a nevus sebaceous. Case Presentation: Herein, we report a 15-year-old adolescent female with a congenital skin lesion on the forehead undergoing surgical excision after changing in size and shape of the lesion. After surgical excision and histopathological examination, a diagnosis of syringocystadenoma papilliferum arising from a sebaceous mole was made. Conclusion: Syringocystadenoma papilliferum is a rare skin tumor. Histological confirmation was required for a definitive diagnosis. Furthermore, surgery and complete removal of the lesion are needed for treatment.