特发性阴囊钙质沉着症的发病与表皮囊肿有关吗?一例印度农村病例报告及文献综述

IF 0.3 Q4 DERMATOLOGY
M. Krishna, S. Dayal
{"title":"特发性阴囊钙质沉着症的发病与表皮囊肿有关吗?一例印度农村病例报告及文献综述","authors":"M. Krishna, S. Dayal","doi":"10.4103/jewd.jewd_32_21","DOIUrl":null,"url":null,"abstract":"Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.","PeriodicalId":17298,"journal":{"name":"Journal of the Egyptian Women's Dermatologic Society","volume":"18 1","pages":"219 - 221"},"PeriodicalIF":0.3000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Idiopathic Scrotal calcinosis cutis – does its pathogenesis link with epidermal cyst? A case report with review of literature from rural India\",\"authors\":\"M. Krishna, S. Dayal\",\"doi\":\"10.4103/jewd.jewd_32_21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.\",\"PeriodicalId\":17298,\"journal\":{\"name\":\"Journal of the Egyptian Women's Dermatologic Society\",\"volume\":\"18 1\",\"pages\":\"219 - 221\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2021-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Egyptian Women's Dermatologic Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jewd.jewd_32_21\",\"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 the Egyptian Women's Dermatologic Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jewd.jewd_32_21","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: 1

摘要

特发性皮肤钙质沉着症的特征是阴囊皮肤上存在多个结节。它们通常见于年轻人,表现为无痛、无症状、圆形和坚固的结节。一名30岁男性表现为无痛性多发阴囊结节。血清钙、磷、降钙素、甲状旁腺激素均在正常范围内。也没有外伤史。临床诊断为皮脂腺囊肿。细针穿刺细胞学检查提示表皮包涵性囊肿。组织病理学检查证实了特发性阴囊钙质病的诊断,提示表皮包涵体的营养不良钙化可能是特发性阴囊钙质病发病的一个起始事件。关于特发性皮肤钙质沉着症与表皮囊肿的关系的文献还不够。因此,本病例报告可以丰富现有数据的不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic Scrotal calcinosis cutis – does its pathogenesis link with epidermal cyst? A case report with review of literature from rural India
Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.
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
CiteScore
0.50
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊介绍: The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信