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1
Functional vagal paraganglioma: a case report illustrating diagnosis and management.功能性迷走神经副神经节瘤:一例说明诊断与治疗的病例报告。
Skull Base. 2010 Nov;20(6):491-6. doi: 10.1055/s-0030-1266761.
2
Perioperative outcomes of syndromic paraganglioma and pheochromocytoma resection in patients with von Hippel-Lindau disease, multiple endocrine neoplasia type 2, or neurofibromatosis type 1.患有冯·希佩尔-林道病、2型多发性内分泌腺瘤病或1型神经纤维瘤病的患者,其综合征性副神经节瘤和嗜铬细胞瘤切除术后的围手术期结局。
Surgery. 2017 Dec;162(6):1259-1269. doi: 10.1016/j.surg.2017.08.002. Epub 2017 Sep 14.
3
Pheochromocytoma and Paraganglioma: Diagnosis, Genetics, and Treatment.嗜铬细胞瘤和副神经节瘤:诊断、遗传学及治疗
Surg Oncol Clin N Am. 2016 Jan;25(1):119-38. doi: 10.1016/j.soc.2015.08.006.
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[Synchronous unilateral vagal paraganglioma and carotid body tumor:one case report].[同步性单侧迷走神经副神经节瘤与颈动脉体瘤:一例报告]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Apr 20;31(8):645-646. doi: 10.13201/j.issn.1001-1781.2017.08.020.
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A functioning catecholamine-secreting vagal body tumor. A case report and review of the literature.
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6
[Clinical profile of pheochromocytoma and paraganglioma with normal plasma free metanephrines].血浆游离甲氧基肾上腺素正常的嗜铬细胞瘤和副神经节瘤的临床特征
Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Aug 18;52(4):614-620. doi: 10.19723/j.issn.1671-167X.2020.04.003.
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Perioperative management of paraganglioma and catecholamine-induced cardiomyopathy in child- a case report and review of the literature.儿童副神经节瘤及儿茶酚胺诱导性心肌病的围手术期管理——病例报告及文献综述
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Insulin Secretion and Insulin Sensitivity Before and After Surgical Treatment of Pheochromocytoma or Paraganglioma.胰岛素分泌和胰岛素敏感性在嗜铬细胞瘤或副神经节瘤手术治疗前后的变化。
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Detection of severe hypertension in a patient with neurofibromatosis type 1 during anesthesia induction: a case report.1型神经纤维瘤病患者麻醉诱导期间严重高血压的检测:一例报告
J Med Case Rep. 2019 Nov 30;13(1):349. doi: 10.1186/s13256-019-2292-4.
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Familial paraganglioma.家族性副神经节瘤
Eur Arch Otorhinolaryngol. 2006 Jan;263(1):23-31. doi: 10.1007/s00405-004-0885-y. Epub 2005 Nov 30.

本文引用的文献

1
Biochemical and clinical responses after treatment of a catecholamine-secreting glomus jugulare tumor with gamma knife radiosurgery.经伽玛刀放射外科手术治疗嗜铬细胞瘤分泌性颈静脉球体瘤后的生化和临床反应。
Head Neck. 2010 Dec;32(12):1720-7. doi: 10.1002/hed.21242.
2
Definitive radiotherapy in the management of paragangliomas arising in the head and neck: a 35-year experience.头颈部副神经节瘤治疗中的根治性放疗:35年经验
Head Neck. 2008 Nov;30(11):1431-8. doi: 10.1002/hed.20885.
3
Phaeochromocytoma.嗜铬细胞瘤
Lancet. 2005;366(9486):665-75. doi: 10.1016/S0140-6736(05)67139-5.
4
Paragangliomas of the head and neck.头颈部副神经节瘤
Oral Oncol. 2004 Jul;40(6):563-75. doi: 10.1016/j.oraloncology.2003.09.004.
5
Pheochromocytoma: state-of-the-art and future prospects.嗜铬细胞瘤:最新进展与未来展望
Endocr Rev. 2003 Aug;24(4):539-53. doi: 10.1210/er.2002-0013.
6
Perioperative management of pheochromocytoma.嗜铬细胞瘤的围手术期管理
J Cardiothorac Vasc Anesth. 2002 Jun;16(3):359-69. doi: 10.1053/jcan.2002.124150.
7
Phaeochromocytoma--recent progress in its management.嗜铬细胞瘤——其治疗的最新进展
Br J Anaesth. 2000 Jul;85(1):44-57. doi: 10.1093/bja/85.1.44.
8
Vagal paraganglioma: the Jefferson experience.迷走神经副神经节瘤:杰斐逊医院的经验
Otolaryngol Head Neck Surg. 2000 Apr;122(4):482-7. doi: 10.1067/mhn.2000.102807.
9
From the archives of the AFIP. Paragangliomas of the head and neck: radiologic-pathologic correlation. Armed Forces Institute of Pathology.源自武装部队病理研究所档案。头颈部副神经节瘤:放射学与病理学相关性。武装部队病理研究所。
Radiographics. 1999 Nov-Dec;19(6):1605-32. doi: 10.1148/radiographics.19.6.g99no251605.
10
Glomus vagale: paraganglioma of the vagus nerve.迷走神经球瘤:迷走神经副神经节瘤。
Laryngoscope. 1994 Apr;104(4):440-5. doi: 10.1288/00005537-199404000-00008.

功能性迷走神经副神经节瘤:一例说明诊断与治疗的病例报告。

Functional vagal paraganglioma: a case report illustrating diagnosis and management.

作者信息

Hornbeek Heidi, Iyer N Gopalakrishna, Carlson Diane L, Stambuk Hilda E, Ryder Mabel, Ganly Ian

出版信息

Skull Base. 2010 Nov;20(6):491-6. doi: 10.1055/s-0030-1266761.

DOI:10.1055/s-0030-1266761
PMID:21772811
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3134809/
Abstract

We report a case of functional vagal paraganglioma to illustrate the biochemical and radiological imaging tests important in diagnosis and to highlight the importance of a multidisciplinary team approach to manage the preoperative, perioperative, and postoperative effects of catecholamine secretion from these tumors.

摘要

我们报告一例功能性迷走神经副神经节瘤,以说明对诊断至关重要的生化和放射影像学检查,并强调多学科团队方法在处理这些肿瘤儿茶酚胺分泌的术前、术中和术后影响方面的重要性。