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右侧肾上腺的类癌样无功能嗜铬细胞瘤:一例报告。

Carcinoma-like nonfunctional pheochromocytoma in the right adrenal gland: A case report.

作者信息

Moriyama Shingo, Takeshita Hideki, Araki Saori, Tokairin Takuo, Kagawa Makoto, Chiba Koji, Adachi Akiko, Noro Akira

机构信息

Department of Urology, Saitama Red Cross Hospital, Saitama 338-8553, Japan.

Department of Pathology, Saitama Red Cross Hospital, Saitama 338-8553, Japan.

出版信息

Oncol Lett. 2016 Aug;12(2):1489-1492. doi: 10.3892/ol.2016.4776. Epub 2016 Jun 23.

DOI:10.3892/ol.2016.4776
PMID:27446458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4950732/
Abstract

Evaluation of the malignant potential of a pheochromocytoma (PCC) remains controversial. PCC is regarded as a neuroendocrine tumor (NET), and the classification of NETs has gradually been defined over the last decade, particularly for gastroenteropancreatic NET. The present study describes a case of locally advanced, carcinoma-like, nonfunctional PCC, which may be regarded as neuroendocrine carcinoma (NEC) rather than a malignant PCC. A 72-year-old man was referred to Saitama Red Cross Hospital (Saitama, Japan), presenting with a 2-month history of right flank pain. Computed tomography revealed a right adrenal gland tumor, which measured 6.0 cm in diameter, invading the hilum of the right kidney, liver and inferior vena cava (IVC). Radical surgery was performed with en bloc resection of the right kidney, and adjacent parts of the liver and IVC. Immunohistochemical examination demonstrated that all of the resected tissues were positive for cytokeratin AE1/AE3, chromogranin A, synaptophysin, cluster of differentiation 56 and Ki-67, and the specimen had a Ki-67 index of 80%. A diagnosis of carcinoma-like PCC or NEC of the adrenal gland was confirmed. Reports of NEC of the adrenal gland are extremely rare in the literature, and classification of PCC as a NET has not yet been fully discussed. The present case may therefore contribute to the classification of NETs in the adrenal gland.

摘要

嗜铬细胞瘤(PCC)恶性潜能的评估仍存在争议。PCC被视为一种神经内分泌肿瘤(NET),在过去十年中,NET的分类逐渐明确,尤其是胃肠胰NET。本研究描述了一例局部晚期、癌样、无功能的PCC病例,该病例可能应被视为神经内分泌癌(NEC)而非恶性PCC。一名72岁男性因右侧胁腹疼痛2个月就诊于日本埼玉红十字医院。计算机断层扫描显示右肾上腺肿瘤,直径6.0 cm,侵犯右肾门、肝脏和下腔静脉(IVC)。行根治性手术,整块切除右肾、肝脏及IVC的相邻部分。免疫组织化学检查显示,所有切除组织的细胞角蛋白AE1/AE3、嗜铬粒蛋白A、突触素、分化簇56和Ki-67均呈阳性,标本的Ki-67指数为80%。确诊为肾上腺癌样PCC或NEC。肾上腺NEC的文献报道极为罕见,PCC作为NET的分类尚未得到充分讨论。因此,本病例可能有助于肾上腺NET的分类。

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本文引用的文献

1
Neuroendocrine tumors, version 1.2015.神经内分泌肿瘤,第 1.2015 版。
J Natl Compr Canc Netw. 2015 Jan;13(1):78-108. doi: 10.6004/jnccn.2015.0011.
2
Genitourinary small-cell carcinoma: 11-year treatment experience.泌尿生殖系统小细胞癌:11年治疗经验
Asian J Androl. 2014 Sep-Oct;16(5):705-9. doi: 10.4103/1008-682X.127811.
3
Update on the management of unusual neuroendocrine tumors: pheochromocytoma and paraganglioma, medullary thyroid cancer and adrenocortical carcinoma.神经内分泌肿瘤的治疗进展:嗜铬细胞瘤和副神经节瘤、甲状腺髓样癌和肾上腺皮质癌。
Semin Oncol. 2013 Feb;40(1):120-33. doi: 10.1053/j.seminoncol.2012.11.009.
4
Subclinical phaeochromocytoma.亚临床型嗜铬细胞瘤。
Best Pract Res Clin Endocrinol Metab. 2012 Aug;26(4):507-15. doi: 10.1016/j.beem.2011.10.008. Epub 2012 May 22.
5
Pheochromocytomas and paragangliomas: assessment of malignant potential.嗜铬细胞瘤和副神经节瘤:恶性潜能评估。
Endocrine. 2011 Dec;40(3):354-65. doi: 10.1007/s12020-011-9545-3. Epub 2011 Oct 25.
6
Neuroendocrine tumors of midgut and hindgut origin: tumor-node-metastasis classification determines clinical outcome.来源于中肠和后肠的神经内分泌肿瘤:肿瘤-淋巴结-转移分类决定临床结局。
Cancer. 2011 Aug 1;117(15):3332-41. doi: 10.1002/cncr.25855. Epub 2011 Jan 18.
7
Adrenal and extra-adrenal nonfunctioning composite pheochromocytoma/paraganglioma with immunohistochemical ectopic hormone expression: comparison of two cases.肾上腺及肾上腺外无功能复合性嗜铬细胞瘤/副神经节瘤伴免疫组化异位激素表达:两例病例比较
Urol Int. 2010;85(3):368-72. doi: 10.1159/000317312. Epub 2010 Sep 9.
8
The NANETS consensus guidelines for the diagnosis and management of poorly differentiated (high-grade) extrapulmonary neuroendocrine carcinomas.《神经内分泌肿瘤治疗国际协作组(NANETS)关于低分化(高级别)肺外神经内分泌癌诊断和治疗的共识指南》。
Pancreas. 2010 Aug;39(6):799-800. doi: 10.1097/MPA.0b013e3181ebb56f.
9
The pathologic classification of neuroendocrine tumors: a review of nomenclature, grading, and staging systems.神经内分泌肿瘤的病理学分类:命名法、分级和分期系统综述。
Pancreas. 2010 Aug;39(6):707-12. doi: 10.1097/MPA.0b013e3181ec124e.
10
A case report of metastatic neuroendocrine carcinoma of the right adrenal gland successfully treated with chemotherapy and surgery.右肾上腺转移神经内分泌癌成功接受化疗和手术治疗的病例报告。
Int J Clin Oncol. 2010 Aug;15(4):423-7. doi: 10.1007/s10147-010-0051-z. Epub 2010 Mar 11.