• 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

[一例膀胱憩室癌病例]

[A case of carcinoma of the bladder diverticulum].

作者信息

Okamura T, Watanabe H, Ueda K, Otaguro K, Nakamura T

出版信息

Hinyokika Kiyo. 1983 Jan;29(1):67-72.

PMID:6428192
Abstract

Carcinoma of the bladder diverticulum is a relatively rare disease. However, its preoperative diagnosis is often difficult. Also, infiltration occurs easily because the diverticulum wall is thin, and prognosis is said to be relatively poor. Histologically, the occurrence rate of squamous cell carcinoma is markedly high. We have experienced a case of squamous cell carcinoma in the bladder diverticulum occurring simultaneously with transitional cell carcinoma of the bladder; and, report this case along with a review of the literature. The patient, a 79-year-old male, had sudden macroscopic hematuria on December 15, 1980, and went to the urology department of a separate hospital. IVU showed distortion of the right ureter, and the patient was referred to our hospital. Cystoscopy revealed a diverticulum in the right wall of the bladder. In the posterior wall of the bladder 2 papillary sessile tumors were also detected. Pathological diagnosis by cold punch biopsy done after the patient was admitted to hospital revealed a grade III transitional cell carcinoma. Total cystectomy + bilateral cutaneous ureterostomy was performed. The diverticulum was in the right wall of the bladder and a papillary sessile tumor with a diameter of 4 cm was found in the diverticulum. A papillary sessile tumor 2 cm in diameter was found in the left bladder wall. Histopathological diagnosis of the tumor in the diverticulum was squamous cell carcinoma ( pG2 , pT3b , ly1, v(-) INF beta) and that of the tumor in the bladder was transitional cell carcinoma ( ( pG3 , pT2 , ly1, v(-), INF gamma).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

膀胱憩室癌是一种相对罕见的疾病。然而,其术前诊断往往困难。此外,由于憩室壁薄,容易发生浸润,据说预后相对较差。组织学上,鳞状细胞癌的发生率明显较高。我们遇到过一例膀胱憩室鳞状细胞癌与膀胱移行细胞癌同时发生的病例;并报告此病例并复习文献。患者为79岁男性,1980年12月15日突然出现肉眼血尿,前往另一家医院的泌尿外科就诊。静脉肾盂造影显示右输尿管扭曲,患者被转诊至我院。膀胱镜检查发现膀胱右壁有一个憩室。在膀胱后壁还发现了2个乳头状无蒂肿瘤。患者入院后经冷切活检的病理诊断为III级移行细胞癌。行全膀胱切除术+双侧皮肤输尿管造口术。憩室位于膀胱右壁,在憩室内发现一个直径4cm的乳头状无蒂肿瘤。在膀胱左壁发现一个直径2cm的乳头状无蒂肿瘤。憩室内肿瘤的组织病理学诊断为鳞状细胞癌(pG2,pT3b,ly1,v(-),INFβ),膀胱内肿瘤的组织病理学诊断为移行细胞癌(pG3,pT2,ly1,v(-),INFγ)。(摘要截短至250字)

相似文献

1
[A case of carcinoma of the bladder diverticulum].[一例膀胱憩室癌病例]
Hinyokika Kiyo. 1983 Jan;29(1):67-72.
2
[Primary carcinoma in diverticulum of the bladder: a report of three cases].膀胱憩室内原发性癌:三例报告
Hinyokika Kiyo. 1992 Jun;38(6):715-9.
3
[Three cases of transitional cell carcinoma in bladder diverticulum treated by a bladder-preserving approach].[三例膀胱憩室内移行细胞癌采用保膀胱方法治疗]
Hinyokika Kiyo. 1999 Feb;45(2):111-3.
4
[A case of true carcinosarcoma in bladder diverticulum].[膀胱憩室内真性癌肉瘤1例]
Hinyokika Kiyo. 1999 Apr;45(4):265-8.
5
[A case of squamous cell carcinoma arising in the urinary bladder diverticulum].[一例发生于膀胱憩室的鳞状细胞癌]
Hinyokika Kiyo. 2000 Aug;46(8):553-5.
6
[Transitional cell carcinoma of the ureter with inverted proliferation accompanied with papillary bladder tumor: a case report].[输尿管移行细胞癌伴内翻性增生并伴有乳头状膀胱肿瘤:一例报告]
Hinyokika Kiyo. 2001 Dec;47(12):861-3.
7
[Primary carcinoma in a diverticulum of the bladder: a report of two cases].[膀胱憩室内原发性癌:两例报告]
Hinyokika Kiyo. 1987 May;33(5):779-85.
8
[A case of transitional cell carcinoma with squamous differentiation which developed squamous cell carcinoma in situ in the clinical course].一例具有鳞状分化的移行细胞癌在临床病程中发生原位鳞状细胞癌的病例
Hinyokika Kiyo. 2006 Sep;52(9):715-8.
9
[Leiomyosarcoma and transitional cell carcinoma in the urinary bladder: a case report].[膀胱平滑肌肉瘤与移行细胞癌:一例报告]
Hinyokika Kiyo. 2002 Mar;48(3):159-62.
10
[Bladder tumor associated with von Recklinghausen's neurofibromatosis: a case report].
Hinyokika Kiyo. 1995 Jan;41(1):61-4.