{"title":"乳头状淋巴管囊腺瘤与乳突、皮脂腺及鳞状细胞癌有关","authors":"Rubal Jain, Sandeep S. Ojha, Abhishek Sharma","doi":"10.4103/ijdpdd.ijdpdd_32_17","DOIUrl":null,"url":null,"abstract":"Syringocystadenoma papilliferum (SCAP) is a rare skin adnexal neoplasm of apocrine gland. One-third of SCAP cases are associated with nevus of Jadassohn. Its transition to squamous cell carcinoma is a rare entity. A strong clinical acumen, prompt excision, and confirmation by histopathology underline treatment of this cutaneous tumor. We report a case of this rare association in the deltoid region of a 55-year-old female.","PeriodicalId":423971,"journal":{"name":"Indian Journal of Dermatopathology and Diagnostic Dermatology","volume":"443 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Syringocystadenoma papilliferum associated with naves sebaceous of jadassohn and squamous cell carcinoma\",\"authors\":\"Rubal Jain, Sandeep S. Ojha, Abhishek Sharma\",\"doi\":\"10.4103/ijdpdd.ijdpdd_32_17\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Syringocystadenoma papilliferum (SCAP) is a rare skin adnexal neoplasm of apocrine gland. One-third of SCAP cases are associated with nevus of Jadassohn. Its transition to squamous cell carcinoma is a rare entity. A strong clinical acumen, prompt excision, and confirmation by histopathology underline treatment of this cutaneous tumor. We report a case of this rare association in the deltoid region of a 55-year-old female.\",\"PeriodicalId\":423971,\"journal\":{\"name\":\"Indian Journal of Dermatopathology and Diagnostic Dermatology\",\"volume\":\"443 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Dermatopathology and Diagnostic Dermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ijdpdd.ijdpdd_32_17\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Dermatopathology and Diagnostic Dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijdpdd.ijdpdd_32_17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Syringocystadenoma papilliferum associated with naves sebaceous of jadassohn and squamous cell carcinoma
Syringocystadenoma papilliferum (SCAP) is a rare skin adnexal neoplasm of apocrine gland. One-third of SCAP cases are associated with nevus of Jadassohn. Its transition to squamous cell carcinoma is a rare entity. A strong clinical acumen, prompt excision, and confirmation by histopathology underline treatment of this cutaneous tumor. We report a case of this rare association in the deltoid region of a 55-year-old female.
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