特发性息肉样阴囊钙质增多症导致睾丸肿瘤诊断延误

A. Bhatnagar, V. Verma, Vishal Purohit
{"title":"特发性息肉样阴囊钙质增多症导致睾丸肿瘤诊断延误","authors":"A. Bhatnagar, V. Verma, Vishal Purohit","doi":"10.4103/1116-5898.134536","DOIUrl":null,"url":null,"abstract":"Idiopathic polypoidal scrotal calcinosis (IPSC) is a rare and benign condition with disputed etiology and it is characterized by multiple calcific nodular deposits in scrotal skin. Here we report a case of a 45-year-old male patient with testicular tumor and 7 years history of scrotal calcinosis is reported. Discussed is the delay in diagnosis of testicular tumor due to IPSC and difficulty in performing fine-needle aspiration cytology in such cases. In our case, no evidence of cystic structure was found around calcified materials. It was indicated that IPSC might be idiopathic. In addition, highlighted the importance of meticulous clinical examination to accurately diagnose the clinical entity and avoid delay in treatment. They are slow growing asymptomatic tumors. Complete excision of the lesion along with the involved scrotal skin with scrotoplasty of the residual scrotal skin is the treatment of choice. Reports of such rare calcified scrotal nodular lesions especially when associated with other malignant conditions need publication and the treatment protocol shared among the surgeons.","PeriodicalId":90935,"journal":{"name":"Nigerian journal of surgical sciences : official journal of the Nigerian Section of International College of Surgeons","volume":"24 1","pages":"23 - 27"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Idiopathic polypoidal scrotal calcinosis leading to delay in diagnosis of testicular tumor\",\"authors\":\"A. Bhatnagar, V. Verma, Vishal Purohit\",\"doi\":\"10.4103/1116-5898.134536\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Idiopathic polypoidal scrotal calcinosis (IPSC) is a rare and benign condition with disputed etiology and it is characterized by multiple calcific nodular deposits in scrotal skin. Here we report a case of a 45-year-old male patient with testicular tumor and 7 years history of scrotal calcinosis is reported. Discussed is the delay in diagnosis of testicular tumor due to IPSC and difficulty in performing fine-needle aspiration cytology in such cases. In our case, no evidence of cystic structure was found around calcified materials. It was indicated that IPSC might be idiopathic. In addition, highlighted the importance of meticulous clinical examination to accurately diagnose the clinical entity and avoid delay in treatment. They are slow growing asymptomatic tumors. Complete excision of the lesion along with the involved scrotal skin with scrotoplasty of the residual scrotal skin is the treatment of choice. Reports of such rare calcified scrotal nodular lesions especially when associated with other malignant conditions need publication and the treatment protocol shared among the surgeons.\",\"PeriodicalId\":90935,\"journal\":{\"name\":\"Nigerian journal of surgical sciences : official journal of the Nigerian Section of International College of Surgeons\",\"volume\":\"24 1\",\"pages\":\"23 - 27\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nigerian journal of surgical sciences : official journal of the Nigerian Section of International College of Surgeons\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/1116-5898.134536\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nigerian journal of surgical sciences : official journal of the Nigerian Section of International College of Surgeons","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/1116-5898.134536","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

特发性息肉样阴囊钙化症(IPSC)是一种罕见的良性疾病,其病因有争议,其特征是阴囊皮肤上有多个钙化结节沉积。我们报告一例45岁男性睾丸肿瘤患者,有7年阴囊钙质沉着症病史。讨论了由于IPSC导致睾丸肿瘤诊断的延误以及在此类病例中进行细针穿刺细胞学检查的困难。在本病例中,钙化物周围未发现囊性结构的证据。提示IPSC可能是特发性的。此外,强调了细致的临床检查对准确诊断临床实体,避免延误治疗的重要性。它们是生长缓慢的无症状肿瘤。完全切除病变和受累的阴囊皮肤,并用阴囊成形术切除残余的阴囊皮肤是治疗的选择。这种罕见的钙化阴囊结节性病变的报告,特别是当与其他恶性疾病相关时,需要发表,并在外科医生之间共享治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic polypoidal scrotal calcinosis leading to delay in diagnosis of testicular tumor
Idiopathic polypoidal scrotal calcinosis (IPSC) is a rare and benign condition with disputed etiology and it is characterized by multiple calcific nodular deposits in scrotal skin. Here we report a case of a 45-year-old male patient with testicular tumor and 7 years history of scrotal calcinosis is reported. Discussed is the delay in diagnosis of testicular tumor due to IPSC and difficulty in performing fine-needle aspiration cytology in such cases. In our case, no evidence of cystic structure was found around calcified materials. It was indicated that IPSC might be idiopathic. In addition, highlighted the importance of meticulous clinical examination to accurately diagnose the clinical entity and avoid delay in treatment. They are slow growing asymptomatic tumors. Complete excision of the lesion along with the involved scrotal skin with scrotoplasty of the residual scrotal skin is the treatment of choice. Reports of such rare calcified scrotal nodular lesions especially when associated with other malignant conditions need publication and the treatment protocol shared among the surgeons.
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
0
×
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