{"title":"色素性干皮病中的角棘瘤:一个超乎想象的实体","authors":"Radhika K Varma, P. Prathap","doi":"10.4172/2157-7412.1000318","DOIUrl":null,"url":null,"abstract":"Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder, characterized by photosensitivity, pigmentary changes, premature skin aging and increase in risk of developing malignant neoplasms of both skin and eyes. Keratoacanthoma (KA) is a rapidly growing benign skin tumor, occurring primarily in elderly light skinned individuals. Here, we report the occurrence of KA of the nose with an unusual morphology in a 12 year old boy with XP where, such an association of the disease in young age is exceedingly rare.","PeriodicalId":89584,"journal":{"name":"Journal of genetic syndromes & gene therapy","volume":"331 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Keratoacanthoma in Xeroderma Pigmentosum: An Entity Beyond Guess\",\"authors\":\"Radhika K Varma, P. Prathap\",\"doi\":\"10.4172/2157-7412.1000318\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder, characterized by photosensitivity, pigmentary changes, premature skin aging and increase in risk of developing malignant neoplasms of both skin and eyes. Keratoacanthoma (KA) is a rapidly growing benign skin tumor, occurring primarily in elderly light skinned individuals. Here, we report the occurrence of KA of the nose with an unusual morphology in a 12 year old boy with XP where, such an association of the disease in young age is exceedingly rare.\",\"PeriodicalId\":89584,\"journal\":{\"name\":\"Journal of genetic syndromes & gene therapy\",\"volume\":\"331 1\",\"pages\":\"1-2\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of genetic syndromes & gene therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2157-7412.1000318\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of genetic syndromes & gene therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2157-7412.1000318","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Keratoacanthoma in Xeroderma Pigmentosum: An Entity Beyond Guess
Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder, characterized by photosensitivity, pigmentary changes, premature skin aging and increase in risk of developing malignant neoplasms of both skin and eyes. Keratoacanthoma (KA) is a rapidly growing benign skin tumor, occurring primarily in elderly light skinned individuals. Here, we report the occurrence of KA of the nose with an unusual morphology in a 12 year old boy with XP where, such an association of the disease in young age is exceedingly rare.