• 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

胆囊腺肌增生症

Adenomyomatosis of the gallbladder.

作者信息

Yang W G, Wang S S, Weng Y J, Tsay S H, Chen C C, Chiang J H, Su C H, Lee F Y, Lee S D

机构信息

Department of Medicine, Veterans General Hospital-Taipei, Taiwan, R.O.C.

出版信息

Zhonghua Yi Xue Za Zhi (Taipei). 1996 Jul;58(1):12-7.

PMID:8870321
Abstract

BACKGROUND

Adenomyomatosis of the gallbladder in Chinese patients has rarely been analyzed.

METHODS

The clinical, radiological and pathological features of 18 patients with histologically-proven adenomyomatosis, collected during a 5-year period, were retrospectively analyzed.

RESULTS

According to the extent and site of involvement, adenomyomatosis of the gallbladder was conventionally classified into three types: localized, generalized and segmental. In our series, the disease was localized in 17 patients (15 in the fundus and 2 in the neck), generalized in one patient and segmental in none. Only 5 patients showed sonographic features correlative to pathologic findings, and 2 of them were correctly diagnosed before operation. Only mild nonspecific abnormalities of liver function test or urine analysis were noted in some patients with gallbladder adenomyomatosis. The clinical manifestations were not related to coincidental diseases in 11 patients. All these 11 patients, with gallstone in 9 and without in 2, complained of epigastralgia, right upper quadrant abdominal pain or dyspepsia, which relieved all after cholecystectomy.

CONCLUSIONS

Some patients with adenomyomatosis may be symptomatic and relieved by cholecystectomy. In patients with adenomyomatosis of the gallbladder and right upper quadrant pain of abdomen without other explanation, cholecystectomy may be considered. Infrequent accurate diagnosis in Chinese patients calls for a high suspicion of the disease entity in clinical practice.

摘要

背景

很少对中国患者的胆囊腺肌症进行分析。

方法

回顾性分析5年间收集的18例经组织学证实为胆囊腺肌症患者的临床、影像学和病理学特征。

结果

根据受累范围和部位,胆囊腺肌症传统上分为三型:局限型、弥漫型和节段型。在我们的病例系列中,17例患者为局限型(15例位于胆囊底部,2例位于颈部),1例为弥漫型,无节段型。仅5例患者的超声特征与病理结果相关,其中2例在术前得到正确诊断。部分胆囊腺肌症患者仅出现肝功能检查或尿液分析的轻度非特异性异常。11例患者的临床表现与合并疾病无关。这11例患者中,9例有胆囊结石,2例无胆囊结石,均主诉上腹部疼痛、右上腹腹痛或消化不良,胆囊切除术后症状均缓解。

结论

部分胆囊腺肌症患者可能有症状,胆囊切除术后症状可缓解。对于胆囊腺肌症且有右上腹腹痛而无其他原因解释的患者,可考虑行胆囊切除术。中国患者中诊断准确性不高,临床实践中需要高度怀疑该病。

相似文献

1
Adenomyomatosis of the gallbladder.胆囊腺肌增生症
Zhonghua Yi Xue Za Zhi (Taipei). 1996 Jul;58(1):12-7.
2
High risk of gallbladder carcinoma in elderly patients with segmental adenomyomatosis of the gallbladder.胆囊节段性腺肌增生症老年患者患胆囊癌的风险高。
J Exp Clin Cancer Res. 2004 Dec;23(4):593-8.
3
[Diffuse adenomyomatosis of the gallbladder].[胆囊弥漫性腺肌增生症]
Acta Chir Iugosl. 1990;37(2):189-98.
4
Segmental adenomyomatosis of the gallbladder predisposes to cholecystolithiasis.胆囊节段性腺肌增生症易患胆囊结石。
J Hepatobiliary Pancreat Surg. 2004;11(5):342-7. doi: 10.1007/s00534-004-0911-x.
5
Adenomyomatosis of the gallbladder in childhood: report of a case and review of the literature.儿童胆囊腺肌增生症:1例报告并文献复习
Pediatr Dev Pathol. 2005 Sep-Oct;8(5):577-80. doi: 10.1007/s10024-005-0074-z. Epub 2005 Oct 5.
6
[Adenomyomatosis of the gallbladder].[胆囊腺肌增生症]
Orv Hetil. 1999 Jun 6;140(23):1309-10.
7
Image of the month. Diffuse adenomyomatosis of the gallbladder.
Arch Surg. 2008 Nov;143(11):1129, 1130. doi: 10.1001/archsurg.143.11.1129.
8
[Adenomyomatosis of the gallbladder: report of 42 cases].[胆囊腺肌症:42例报告]
Zhonghua Wai Ke Za Zhi. 1994 Jun;32(6):357-60.
9
Diffuse Adenomyomatosis of the Gallbladder in a Child.儿童胆囊弥漫性腺肌增生症
J Pediatr Hematol Oncol. 2016 Nov;38(8):e307-e309. doi: 10.1097/MPH.0000000000000640.
10
Adenomyomatosis of the Gallbladder as a Cause of Recurrent Abdominal Pain.胆囊腺肌增生症作为复发性腹痛的病因
J Pediatr. 2018 Nov;202:328-328.e1. doi: 10.1016/j.jpeds.2018.05.020. Epub 2018 Jun 11.