皮肤黑色素细胞增多症的研究进展

IF 0.2 Q4 DERMATOLOGY Indian Journal of Paediatric Dermatology Pub Date : 2023-01-01 DOI:10.4103/ijpd.ijpd_66_22
Manjyot Gautam, Kajomi Shingala
{"title":"皮肤黑色素细胞增多症的研究进展","authors":"Manjyot Gautam, Kajomi Shingala","doi":"10.4103/ijpd.ijpd_66_22","DOIUrl":null,"url":null,"abstract":"Abstract Dermal melanocytosis is a histological term used to describe a clinical spectrum of cutaneous diseases which present as bluish-gray pigmentation of the skin. The most common forms include the Mongolian spot (MS), nevus of Ota, nevus of Ito, and dermal melanocyte hamartoma sharing similar etiologies and histologic findings but different associations and prognosis. Although these lesions usually resolve by 1 to 2 years of age, widespread aberrant MSs, nevus of Ota, and nevus of Ito can persist into adulthood and can become a great concern for the patients regarding the pigmentation and health risk associated with the same. An extensive literature search was done; all clinical trials, randomized double-blind or single-blind controlled trials, open-label studies, retrospective studies, reviews, case series, and case reports concerned with dermal melanocytosis were screened. The selected articles were retrieved; the final manuscript was prepared, analyzed, and presented in a narrative fashion.","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"17 1","pages":"0"},"PeriodicalIF":0.2000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Review of Dermal Melanocytosis\",\"authors\":\"Manjyot Gautam, Kajomi Shingala\",\"doi\":\"10.4103/ijpd.ijpd_66_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Dermal melanocytosis is a histological term used to describe a clinical spectrum of cutaneous diseases which present as bluish-gray pigmentation of the skin. The most common forms include the Mongolian spot (MS), nevus of Ota, nevus of Ito, and dermal melanocyte hamartoma sharing similar etiologies and histologic findings but different associations and prognosis. Although these lesions usually resolve by 1 to 2 years of age, widespread aberrant MSs, nevus of Ota, and nevus of Ito can persist into adulthood and can become a great concern for the patients regarding the pigmentation and health risk associated with the same. An extensive literature search was done; all clinical trials, randomized double-blind or single-blind controlled trials, open-label studies, retrospective studies, reviews, case series, and case reports concerned with dermal melanocytosis were screened. The selected articles were retrieved; the final manuscript was prepared, analyzed, and presented in a narrative fashion.\",\"PeriodicalId\":13275,\"journal\":{\"name\":\"Indian Journal of Paediatric Dermatology\",\"volume\":\"17 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Paediatric Dermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ijpd.ijpd_66_22\",\"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":"Indian Journal of Paediatric Dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijpd.ijpd_66_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

皮肤黑色素细胞增多症是一个组织学术语,用于描述皮肤疾病的临床谱,其表现为皮肤的蓝灰色色素沉着。最常见的形式包括蒙古斑(MS)、太田痣、伊藤痣和皮肤黑素细胞错构瘤,它们具有相似的病因和组织学表现,但不同的关联和预后。虽然这些病变通常在1至2岁时消退,但广泛的异常MSs、太田痣和伊藤痣可持续到成年,并可能成为患者对色素沉着和相关健康风险的极大关注。进行了广泛的文献检索;筛选了所有与皮肤黑色素细胞增多症有关的临床试验、随机双盲或单盲对照试验、开放标签研究、回顾性研究、综述、病例系列和病例报告。检索选定的文章;最后的手稿被准备、分析,并以叙述的方式呈现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A Review of Dermal Melanocytosis
Abstract Dermal melanocytosis is a histological term used to describe a clinical spectrum of cutaneous diseases which present as bluish-gray pigmentation of the skin. The most common forms include the Mongolian spot (MS), nevus of Ota, nevus of Ito, and dermal melanocyte hamartoma sharing similar etiologies and histologic findings but different associations and prognosis. Although these lesions usually resolve by 1 to 2 years of age, widespread aberrant MSs, nevus of Ota, and nevus of Ito can persist into adulthood and can become a great concern for the patients regarding the pigmentation and health risk associated with the same. An extensive literature search was done; all clinical trials, randomized double-blind or single-blind controlled trials, open-label studies, retrospective studies, reviews, case series, and case reports concerned with dermal melanocytosis were screened. The selected articles were retrieved; the final manuscript was prepared, analyzed, and presented in a narrative fashion.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
27
审稿时长
25 weeks
期刊最新文献
Isolated nail lichen planus in an indian boy A rare case of bilateral xanthelasma palpebrarum in a 12-year-old girl Onychomycosis involving multiple nails in healthy infants - Uncommon but emerging fungal infection Trichotillomania in Children − How can a Dermatologist Deal with it? Sturge–Weber syndrome in childhood lupus complicated by macrophage activation syndrome
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1