• 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

祖克坎德尔器嗜铬细胞瘤

Pheochromocytoma of the organ of Zuckerkandl.

作者信息

Le Hoang Di Thu, Nguyen Thai Thi My Hanh, Pham Anh Vu, Dang Cong Thuan, Nguyen Thanh Thao

机构信息

Department of Radiology, Hue University of Medicine and Pharmacy, Hue University, 06 Ngo Quyen t., Hue, Vietnam.

Department of Surgery, Hue University of Medicine and Pharmacy, Hue University, Hue, Vietnam.

出版信息

Radiol Case Rep. 2020 Nov 28;16(2):268-272. doi: 10.1016/j.radcr.2020.11.024. eCollection 2021 Feb.

DOI:10.1016/j.radcr.2020.11.024
PMID:33299507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7708655/
Abstract

Paragangliomas are uncommon neuroendocrine neoplasms that occur in characteristic locations. While parasympathetic paragangliomas are mainly located at the head and neck, sympathetic paragangliomas are mostly located below the neck. Among parasympathetic paragangliomas, pheochromocytomas are the most common. Ninety percent of cases of pheochromocytomas arise within the adrenal gland. We report a case of a 63-year-old woman with an extra-adrenal pheochromocytoma of the organ of Zuckerkandl detected by CT and MRI and subsequently confirmed by postoperative histology and immunohistochemistry.

摘要

副神经节瘤是一种罕见的神经内分泌肿瘤,发生于特定部位。副交感神经节瘤主要位于头颈部,而交感神经节瘤大多位于颈部以下。在副交感神经节瘤中,嗜铬细胞瘤最为常见。90%的嗜铬细胞瘤病例起源于肾上腺。我们报告一例63岁女性,通过CT和MRI检测出肾上腺外祖克坎德尔器官嗜铬细胞瘤,随后经术后组织学和免疫组化确诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/e07639613cca/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/b4cb690c2ae7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/c02d84e80721/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/0876a9fe0d9c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/36f52768a7b1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/5e74d3e672d5/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/eb77e59cfa86/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/e07639613cca/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/b4cb690c2ae7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/c02d84e80721/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/0876a9fe0d9c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/36f52768a7b1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/5e74d3e672d5/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/eb77e59cfa86/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/7708655/e07639613cca/gr7.jpg

相似文献

1
Pheochromocytoma of the organ of Zuckerkandl.祖克坎德尔器嗜铬细胞瘤
Radiol Case Rep. 2020 Nov 28;16(2):268-272. doi: 10.1016/j.radcr.2020.11.024. eCollection 2021 Feb.
2
Paraganglioma副神经节瘤
3
Pheochromocytoma in the organ of Zuckerkandl with distant skeletal metastases - A case report.肾上腺外嗜铬细胞瘤伴远处骨骼转移——一例报告
Radiol Case Rep. 2024 Jan 29;19(4):1582-1588. doi: 10.1016/j.radcr.2024.01.026. eCollection 2024 Apr.
4
Extra-adrenal pheochromocytoma at the organ of Zuckerkandl: a case report and literature review.祖克坎德尔器处的肾上腺外嗜铬细胞瘤:一例报告及文献综述
Radiol Case Rep. 2017 Mar 21;12(2):343-347. doi: 10.1016/j.radcr.2016.12.009. eCollection 2017 Jun.
5
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.2022 年世卫组织副神经节瘤和嗜铬细胞瘤分类概述。
Endocr Pathol. 2022 Mar;33(1):90-114. doi: 10.1007/s12022-022-09704-6. Epub 2022 Mar 13.
6
Pheochromocytomas and Paragangliomas: An Update on Recent Molecular Genetic Advances and Criteria for Malignancy.嗜铬细胞瘤和副神经节瘤:近期分子遗传学进展及恶性肿瘤标准更新。
Adv Anat Pathol. 2015 Sep;22(5):283-93. doi: 10.1097/PAP.0000000000000086.
7
Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors.患有嗜铬细胞瘤和副神经节瘤的儿科患者除了进行影像学检查以检测肾上腺外和转移性肿瘤外,还应进行常见易感基因的常规术前基因检测。
Surgery. 2017 Jan;161(1):220-227. doi: 10.1016/j.surg.2016.05.059. Epub 2016 Nov 16.
8
Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.在与SDHD相关的头颈部副神经节瘤患者中通过筛查检测到的嗜铬细胞瘤和肾上腺外副神经节瘤
Endocr Relat Cancer. 2009 Jun;16(2):527-36. doi: 10.1677/ERC-09-0024. Epub 2009 Mar 16.
9
Paraganglioma of the Organ of Zuckerkandl.祖克坎德尔器副神经节瘤
J La State Med Soc. 2012 Jan-Feb;164(1):26-30.
10
Sporadic paraganglioma.散发性副神经节瘤
World J Surg. 2008 May;32(5):683-7. doi: 10.1007/s00268-007-9360-4.

引用本文的文献

1
Surgical Management of Paraganglioma of the Organ of Zuckerkandl with Combined Resection of the Aorta and Inferior Vena Cava with Bifurcation: A Case Report.伴主动脉及下腔静脉分叉联合切除的祖克坎德尔器副神经节瘤的手术治疗:一例报告
Vasc Specialist Int. 2025 Mar 4;41:3. doi: 10.5758/vsi.240099.
2
Pheochromocytoma in the organ of Zuckerkandl with distant skeletal metastases - A case report.肾上腺外嗜铬细胞瘤伴远处骨骼转移——一例报告
Radiol Case Rep. 2024 Jan 29;19(4):1582-1588. doi: 10.1016/j.radcr.2024.01.026. eCollection 2024 Apr.

本文引用的文献

1
Pheochromocytoma and Paraganglioma: From Epidemiology to Clinical Findings.嗜铬细胞瘤和副神经节瘤:从流行病学到临床发现
Sisli Etfal Hastan Tip Bul. 2020 Jun 3;54(2):159-168. doi: 10.14744/SEMB.2020.18794. eCollection 2020.
2
Genetics and imaging of pheochromocytomas and paragangliomas: current update.嗜铬细胞瘤和副神经节瘤的遗传学和影像学:最新研究进展。
Abdom Radiol (NY). 2020 Apr;45(4):928-944. doi: 10.1007/s00261-019-02044-w.
3
The Diagnosis and Clinical Significance of Paragangliomas in Unusual Locations.罕见部位副神经节瘤的诊断及临床意义
J Clin Med. 2018 Sep 13;7(9):280. doi: 10.3390/jcm7090280.
4
Old, New, and Emerging Immunohistochemical Markers in Pheochromocytoma and Paraganglioma.《嗜铬细胞瘤和副神经节瘤中的新旧及新兴免疫组化标志物》
Endocr Pathol. 2018 Jun;29(2):169-175. doi: 10.1007/s12022-018-9534-7.
5
Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours.2017 年世界卫生组织(WHO)内分泌肿瘤学肾上腺肿瘤更新。
Endocr Pathol. 2017 Sep;28(3):213-227. doi: 10.1007/s12022-017-9484-5.
6
Multi-modality imaging of pheochromocytoma.嗜铬细胞瘤的多模态成像
Radiol Case Rep. 2015 Dec 7;7(4):770. doi: 10.2484/rcr.v7i4.770. eCollection 2012.
7
15 YEARS OF PARAGANGLIOMA: Pathology of pheochromocytoma and paraganglioma.副神经节瘤的15年研究:嗜铬细胞瘤和副神经节瘤的病理学
Endocr Relat Cancer. 2015 Aug;22(4):T123-33. doi: 10.1530/ERC-15-0261. Epub 2015 Jul 1.
8
Pheochromocytoma: the range of appearances on ultrasound, CT, MRI, and functional imaging.嗜铬细胞瘤:超声、CT、MRI 和功能成像的表现范围。
AJR Am J Roentgenol. 2013 Feb;200(2):370-8. doi: 10.2214/AJR.12.9126.
9
Radiological imaging in endocrine hypertension.内分泌性高血压的放射影像学检查
Indian J Endocrinol Metab. 2011 Oct;15 Suppl 4(Suppl4):S383-8. doi: 10.4103/2230-8210.86984.
10
The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer.北美神经内分泌肿瘤学会共识指南:神经内分泌肿瘤的诊断和管理-嗜铬细胞瘤、副神经节瘤和甲状腺髓样癌。
Pancreas. 2010 Aug;39(6):775-83. doi: 10.1097/MPA.0b013e3181ebb4f0.