Amr Abduljabbar , Mohammad Kamrul Ahsan , Mohammed A. Buraik , Khalid Al Attas , Amr Gamal , Sanjay Kumar
{"title":"幼年黄色肉芽肿:晚期表现为巨大形态，以萎缩性后遗症结束:1例报告","authors":"Amr Abduljabbar , Mohammad Kamrul Ahsan , Mohammed A. Buraik , Khalid Al Attas , Amr Gamal , Sanjay Kumar","doi":"10.1016/j.jdds.2014.06.001","DOIUrl":null,"url":null,"abstract":"<div><p>Juvenile xanthogranuloma (JXG) is a histiocytic disorder that is usually benign and limited to the skin. Usually it regresses spontaneously, more often without or with limited skin changes. The systemic form of JXG is rare and may be associated with severe morbidity and mortality due to CNS involvement. Here, we describe a 15<!--> <!-->year old boy with puzzling skin lesions evolving since last 6<!--> <!-->months on the neck. A skin biopsy and immunohistochemistry confirmed the diagnosis of JXG.</p></div>","PeriodicalId":43409,"journal":{"name":"Journal of Dermatology & Dermatologic Surgery-JDDS","volume":"19 1","pages":"Pages 47-50"},"PeriodicalIF":0.2000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jdds.2014.06.001","citationCount":"0","resultStr":"{\"title\":\"Juvenile xanthogranuloma: Late presentation of giant form ends with atrophic sequelae: Case report\",\"authors\":\"Amr Abduljabbar , Mohammad Kamrul Ahsan , Mohammed A. Buraik , Khalid Al Attas , Amr Gamal , Sanjay Kumar\",\"doi\":\"10.1016/j.jdds.2014.06.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Juvenile xanthogranuloma (JXG) is a histiocytic disorder that is usually benign and limited to the skin. Usually it regresses spontaneously, more often without or with limited skin changes. The systemic form of JXG is rare and may be associated with severe morbidity and mortality due to CNS involvement. Here, we describe a 15<!--> <!-->year old boy with puzzling skin lesions evolving since last 6<!--> <!-->months on the neck. A skin biopsy and immunohistochemistry confirmed the diagnosis of JXG.</p></div>\",\"PeriodicalId\":43409,\"journal\":{\"name\":\"Journal of Dermatology & Dermatologic Surgery-JDDS\",\"volume\":\"19 1\",\"pages\":\"Pages 47-50\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.jdds.2014.06.001\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Dermatology & Dermatologic Surgery-JDDS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352241014000139\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Dermatology & Dermatologic Surgery-JDDS","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352241014000139","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DERMATOLOGY","Score":null,"Total":0}
Juvenile xanthogranuloma: Late presentation of giant form ends with atrophic sequelae: Case report
Juvenile xanthogranuloma (JXG) is a histiocytic disorder that is usually benign and limited to the skin. Usually it regresses spontaneously, more often without or with limited skin changes. The systemic form of JXG is rare and may be associated with severe morbidity and mortality due to CNS involvement. Here, we describe a 15 year old boy with puzzling skin lesions evolving since last 6 months on the neck. A skin biopsy and immunohistochemistry confirmed the diagnosis of JXG.
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