• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

膀胱非典型颗粒细胞瘤病例报告

A case report of atypical granular cell tumor of bladder.

作者信息

Movahed Saeed, Amiri Ahmad Janatmakan, Kalkali Abdol-Rahman

机构信息

Zahedan University of Medical Science, Zahedan, Iran.

Zahedan University of Medical Science, Zahedan, Iran.

出版信息

Int J Surg Case Rep. 2024 Aug;121:109980. doi: 10.1016/j.ijscr.2024.109980. Epub 2024 Jul 1.

DOI:10.1016/j.ijscr.2024.109980
PMID:38959614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11268323/
Abstract

INTRODUCTION AND IMPORTANCE

The development of granular cell tumor (GCT) in urinary bladder is a very rare disorder.

CASE PRESENTATION

We reported a 50-year-old male, who was referred with vague pelvic pain. There was a hypoechoic mass with diameters of 30*25 mm in frontal wall of bladder in the sonogram.

CLINICAL DISCUSSION

The patient underwent transurethral resection of the bladder tumor. Subsequent pathology and immunohistochemistry findings supported the diagnosis of atypical GCT.

CONCLUSION

The patient was tumor-free at the follow up. It seems that GCT is usually benign in nature and can be treated by excisional surgery.

摘要

引言与重要性

膀胱颗粒细胞瘤(GCT)的发生是一种非常罕见的病症。

病例介绍

我们报告了一名50岁男性,因盆腔隐痛前来就诊。超声检查显示膀胱前壁有一个直径为30×25毫米的低回声肿块。

临床讨论

患者接受了经尿道膀胱肿瘤切除术。随后的病理和免疫组化结果支持非典型GCT的诊断。

结论

随访时患者无肿瘤。GCT似乎通常本质上是良性的,可通过切除手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6a/11268323/f734d994bec6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6a/11268323/f734d994bec6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f6a/11268323/f734d994bec6/gr1.jpg

相似文献

1
A case report of atypical granular cell tumor of bladder.膀胱非典型颗粒细胞瘤病例报告
Int J Surg Case Rep. 2024 Aug;121:109980. doi: 10.1016/j.ijscr.2024.109980. Epub 2024 Jul 1.
2
Atypical granular cell tumor of the urinary bladder: A case report.膀胱非典型颗粒细胞瘤:一例报告。
World J Clin Cases. 2021 Oct 6;9(28):8453-8460. doi: 10.12998/wjcc.v9.i28.8453.
3
A case report of rare granular cell tumor of the urinary bladder.膀胱罕见颗粒细胞瘤一例报告
Urol Case Rep. 2022 Feb 16;42:102034. doi: 10.1016/j.eucr.2022.102034. eCollection 2022 May.
4
Granular cell tumor of the urinary bladder.膀胱颗粒细胞瘤
Korean J Urol. 2010 Apr;51(4):291-3. doi: 10.4111/kju.2010.51.4.291. Epub 2010 Apr 21.
5
Granular Cell Tumor of the Bladder: A Report of Six Cases.膀胱颗粒细胞瘤:6例报告
Urology. 2018 Nov;121:203.e1-203.e5. doi: 10.1016/j.urology.2018.08.018. Epub 2018 Aug 29.
6
Atypical granular cell tumor of the urinary bladder: A case report and literature review.膀胱非典型颗粒细胞瘤:一例报告及文献复习
Urol Case Rep. 2021 Mar 29;38:101669. doi: 10.1016/j.eucr.2021.101669. eCollection 2021 Sep.
7
Granular cell tumor of the bladder: a case report.膀胱颗粒细胞瘤:一例报告
Anal Quant Cytopathol Histpathol. 2013 Oct;35(5):289-93.
8
Bladder leiomyoma treated with transurethral resection of bladder tumor (TURBT): Case report.经尿道膀胱肿瘤切除术(TURBT)治疗膀胱平滑肌瘤:病例报告
Int J Surg Case Rep. 2022 Sep;98:107464. doi: 10.1016/j.ijscr.2022.107464. Epub 2022 Jul 30.
9
Granular cell tumor coexisting with adenocarcinoma in the stomach: Report of a rare case.胃颗粒细胞瘤与腺癌共存:1例罕见病例报告
Ann Med Surg (Lond). 2021 Apr 26;65:102271. doi: 10.1016/j.amsu.2021.102271. eCollection 2021 May.
10
Granular cell tumour of the urinary bladder: a case report and review of the literature.膀胱颗粒细胞瘤:一例报告并文献复习
Arch Ital Urol Androl. 2007 Mar;79(1):43-4.

引用本文的文献

1
Atypical granular cell tumour of urinary bladder - case report of an extremely rare neoplasm.膀胱非典型颗粒细胞瘤——一种极其罕见肿瘤的病例报告
Cent European J Urol. 2024;77(4):637-640. doi: 10.5173/ceju.2024.153. Epub 2024 Nov 10.
2
Atypical Multifocal Granular Cell Tumor with FLT3 Y842C Somatic Mutation: A case report and a review of the literature.伴有 FLT3 Y842C 体细胞突变的非典型多灶性颗粒细胞瘤:病例报告及文献复习。
Tunis Med. 2024 Oct 5;102(10):730-734. doi: 10.62438/tunismed.v102i10.5172.