膀胱副神经节瘤2例报告并文献复习

A. Slaoui, Babty Mouftah, A. Slaoui, Y. Himmi, Amine El Affari, O. Zineddine, Taha Yassine Abboudech, Z. Bernoussi, T. Karmouni, K. El khader, Aziz Baydada, A. Kharbach, A. Koutani, Ahmen Ibn Attya Andaloussi
{"title":"膀胱副神经节瘤2例报告并文献复习","authors":"A. Slaoui, Babty Mouftah, A. Slaoui, Y. Himmi, Amine El Affari, O. Zineddine, Taha Yassine Abboudech, Z. Bernoussi, T. Karmouni, K. El khader, Aziz Baydada, A. Kharbach, A. Koutani, Ahmen Ibn Attya Andaloussi","doi":"10.59657/2837-8172.brs.23.004","DOIUrl":null,"url":null,"abstract":"Objective: We report two incidental cases of bladder paraganglioma and a review of the literature published to date. Methods: Medline was searched for the last 10 years for the terms \"paraganglioma\" and \"urinary\" and \"bladder\". Results: Bladder paraganglioma (BP) is extremely rare. It represents 10% of all paragangliomas and concerns less than 0.06% of bladder tumors. Often discovered by chance, it can nevertheless be symptomatic, particularly during micturition. The most common symptoms are hematuria, hypertension and headache. About 14% of these tumors are malignant and radio-chemically resistant. Surgery is therefore the cornerstone of treatment. We recommend, cystoscopy, partial cystectomy and regular follow-up based on regular cystoscopy and imaging. Their rarity explains why, at present, there are no recommendations for treatment and monitoring. However, their risk of malignancy recurrence and metastasis requires regular and long-term follow-up. Conclusions: Bladder paragangliomas are rare tumors. Treatment should be based on partial cystectomy and their follow-up should be regular.","PeriodicalId":13694,"journal":{"name":"International Journal of Medical Reviews and Case Reports","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bladder Paraganglioma: Report of Two Cases and A Literature Review\",\"authors\":\"A. Slaoui, Babty Mouftah, A. Slaoui, Y. Himmi, Amine El Affari, O. Zineddine, Taha Yassine Abboudech, Z. Bernoussi, T. Karmouni, K. El khader, Aziz Baydada, A. Kharbach, A. Koutani, Ahmen Ibn Attya Andaloussi\",\"doi\":\"10.59657/2837-8172.brs.23.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: We report two incidental cases of bladder paraganglioma and a review of the literature published to date. Methods: Medline was searched for the last 10 years for the terms \\\"paraganglioma\\\" and \\\"urinary\\\" and \\\"bladder\\\". Results: Bladder paraganglioma (BP) is extremely rare. It represents 10% of all paragangliomas and concerns less than 0.06% of bladder tumors. Often discovered by chance, it can nevertheless be symptomatic, particularly during micturition. The most common symptoms are hematuria, hypertension and headache. About 14% of these tumors are malignant and radio-chemically resistant. Surgery is therefore the cornerstone of treatment. We recommend, cystoscopy, partial cystectomy and regular follow-up based on regular cystoscopy and imaging. Their rarity explains why, at present, there are no recommendations for treatment and monitoring. However, their risk of malignancy recurrence and metastasis requires regular and long-term follow-up. Conclusions: Bladder paragangliomas are rare tumors. Treatment should be based on partial cystectomy and their follow-up should be regular.\",\"PeriodicalId\":13694,\"journal\":{\"name\":\"International Journal of Medical Reviews and Case Reports\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Medical Reviews and Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.59657/2837-8172.brs.23.004\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Medical Reviews and Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59657/2837-8172.brs.23.004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:我们报告两例膀胱副神经节瘤的偶发病例,并回顾迄今为止发表的文献。方法:在Medline检索近10年的“副神经节瘤”、“泌尿系统”和“膀胱”等术语。结果:膀胱副神经节瘤(BP)极为罕见。它占所有副神经节瘤的10%,占膀胱肿瘤的不到0.06%。它通常是偶然发现的,但也可能是有症状的,特别是在排尿时。最常见的症状是血尿、高血压和头痛。这些肿瘤中约有14%是恶性的,具有放射化学抗性。因此,手术是治疗的基石。我们建议患者行膀胱镜检查、部分膀胱切除术,并在常规膀胱镜检查和影像学检查的基础上定期随访。它们的罕见性解释了为什么目前没有关于治疗和监测的建议。然而,他们的恶性复发和转移的风险需要定期和长期的随访。结论:膀胱副神经节瘤是一种罕见的肿瘤。治疗应以部分膀胱切除术为基础,并定期随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bladder Paraganglioma: Report of Two Cases and A Literature Review
Objective: We report two incidental cases of bladder paraganglioma and a review of the literature published to date. Methods: Medline was searched for the last 10 years for the terms "paraganglioma" and "urinary" and "bladder". Results: Bladder paraganglioma (BP) is extremely rare. It represents 10% of all paragangliomas and concerns less than 0.06% of bladder tumors. Often discovered by chance, it can nevertheless be symptomatic, particularly during micturition. The most common symptoms are hematuria, hypertension and headache. About 14% of these tumors are malignant and radio-chemically resistant. Surgery is therefore the cornerstone of treatment. We recommend, cystoscopy, partial cystectomy and regular follow-up based on regular cystoscopy and imaging. Their rarity explains why, at present, there are no recommendations for treatment and monitoring. However, their risk of malignancy recurrence and metastasis requires regular and long-term follow-up. Conclusions: Bladder paragangliomas are rare tumors. Treatment should be based on partial cystectomy and their follow-up should be regular.
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