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膀胱恶性副神经节瘤:预后指标的免疫组织化学研究

Malignant paraganglioma of the urinary bladder: Immunohistochemical study of prognostic indicators.

作者信息

Kovacs Kalman, Bell David, Gardiner Geoffrey W, Honey R John, Goguen Jeannette, Rotondo Fabio

机构信息

Department of Laboratory Medicine, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.

出版信息

Endocr Pathol. 2005 Winter;16(4):363-9. doi: 10.1385/ep:16:4:363.

DOI:10.1385/ep:16:4:363
PMID:16627923
Abstract

Using various immunohistochemical markers, the objective of our study was to assess whether correlation exists between growth potential of paraganglioma (pheochromocytoma) cells and formation of metastasis. The patient was a 28-yr-old man who presented with intermittent episodes of gross hematuria due to a mass in the urinary bladder. He had no constitutional symptoms to suggest paraganglioma. Histologic, immunohistochemical, and electron microscopic investigation of the surgically removed tissue proved that the tumor was a malignant paraganglioma with metastases in the regional lymph nodes. The immunohistochemical tests were not supportive of high cell proliferation index, indicating that metastases can develop in the absence of rapid multiplication of the tumor cells. Abnormalities in vascular architecture and marked expression of VEGF in the tumor cells may be regarded as prognostic signs to predict the formation of metastases.

摘要

我们使用各种免疫组织化学标志物进行研究,目的是评估副神经节瘤(嗜铬细胞瘤)细胞的生长潜能与转移形成之间是否存在相关性。该患者为一名28岁男性,因膀胱肿物出现间歇性肉眼血尿。他没有提示副神经节瘤的全身症状。对手术切除组织进行的组织学、免疫组织化学和电子显微镜检查证明,该肿瘤是恶性副神经节瘤,伴有区域淋巴结转移。免疫组织化学检测不支持高细胞增殖指数,这表明在肿瘤细胞没有快速增殖的情况下也可能发生转移。肿瘤血管结构异常以及肿瘤细胞中VEGF的显著表达可被视为预测转移形成的预后指标。

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Malignant paraganglioma of the urinary bladder: Immunohistochemical study of prognostic indicators.膀胱恶性副神经节瘤:预后指标的免疫组织化学研究
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引用本文的文献

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Potential Biomarkers of Metastasizing Paragangliomas and Pheochromocytomas.转移性副神经节瘤和嗜铬细胞瘤的潜在生物标志物。
Life (Basel). 2021 Nov 4;11(11):1179. doi: 10.3390/life11111179.
2
Ectopic Cushing's Syndrome Secondary to Metastatic Paraganglioma.转移性副神经节瘤继发异位库欣综合征
Case Rep Endocrinol. 2021 Jun 24;2021:5593920. doi: 10.1155/2021/5593920. eCollection 2021.
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Non-functional paraganglioma of urinary bladder managed by transurethral resection.经尿道切除治疗膀胱非功能性副神经节瘤。

本文引用的文献

1
Histological grading of adrenal and extra-adrenal pheochromocytomas and relationship to prognosis: a clinicopathological analysis of 116 adrenal pheochromocytomas and 30 extra-adrenal sympathetic paragangliomas including 38 malignant tumors.肾上腺及肾上腺外嗜铬细胞瘤的组织学分级及其与预后的关系:116例肾上腺嗜铬细胞瘤和30例肾上腺外交感神经节旁瘤(包括38例恶性肿瘤)的临床病理分析
Endocr Pathol. 2005 Spring;16(1):23-32. doi: 10.1385/ep:16:1:023.
2
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.SDHB基因的突变与肾上腺外和/或恶性嗜铬细胞瘤相关。
Cancer Res. 2003 Sep 1;63(17):5615-21.
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Int Braz J Urol. 2019 Sep-Oct;45(5):910-915. doi: 10.1590/S1677-5538.IBJU.2018.0604.
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Neuroendocrine Tumors of the Urinary Bladder According to the 2016 World Health Organization Classification: Molecular and Clinical Characteristics.根据2016年世界卫生组织分类的膀胱神经内分泌肿瘤:分子与临床特征
Endocr Pathol. 2016 Sep;27(3):188-99. doi: 10.1007/s12022-016-9444-5.
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Non-Functional Paraganglioma of the Urinary Bladder Treated by Transurethral Resection: Report of Two Cases.经尿道切除术治疗膀胱非功能性副神经节瘤:2例报告
J Clin Diagn Res. 2016 Feb;10(2):XD01-XD03. doi: 10.7860/JCDR/2016/17953.7219. Epub 2016 Feb 1.
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Non-functioning paraganglioma of the urinary bladder: A case report and review of the literature.膀胱无功能副神经节瘤:一例报告并文献复习
Oncol Lett. 2014 Mar;7(3):891-893. doi: 10.3892/ol.2014.1790. Epub 2014 Jan 10.
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Non-functional paraganglioma of the urinary bladder: a case report.膀胱无功能副神经节瘤:一例报告
J Med Case Rep. 2010 Jul 19;4:216. doi: 10.1186/1752-1947-4-216.
Pheochromocytoma of the urinary bladder.
膀胱嗜铬细胞瘤
N Engl J Med. 1953 Jul 2;249(1):25-6. doi: 10.1056/NEJM195307022490106.
4
Angiogenesis and vascular architecture in pheochromocytomas: distinctive traits in malignant tumors.嗜铬细胞瘤中的血管生成与血管结构:恶性肿瘤的独特特征
Am J Pathol. 2002 Oct;161(4):1235-46. doi: 10.1016/S0002-9440(10)64400-8.
5
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma.一个明显散发的嗜铬细胞瘤中SDHB基因突变的功能后果
J Clin Endocrinol Metab. 2002 Oct;87(10):4771-4. doi: 10.1210/jc.2002-020525.
6
Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene.伴有琥珀酸脱氢酶B基因突变且生存期延长的家族性恶性分泌儿茶酚胺副神经节瘤。
J Clin Endocrinol Metab. 2002 Sep;87(9):4101-5. doi: 10.1210/jc.2002-020312.
7
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J Clin Pathol. 2001 Jun;54(6):443-8. doi: 10.1136/jcp.54.6.443.
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Am J Pathol. 2000 Aug;157(2):353-9. doi: 10.1016/S0002-9440(10)64547-6.