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1
Hereditary paraganglioma of the nasopharynx.鼻咽部遗传性副神经节瘤
Head Neck Pathol. 2008 Dec;2(4):272-8. doi: 10.1007/s12105-008-0090-1. Epub 2008 Nov 9.
2
[Neoplastic involvement of the cranial base. Role of computerized tomography and magnetic resonance].[颅底的肿瘤累及。计算机断层扫描和磁共振成像的作用]
Clin Ter. 1994 Oct;145(10):295-302.
3
Multiple paraganglioma syndrome type 4 due to succinate dehydrogenase B mutation: diagnostic and therapeutic challenges of a skull base paraganglioma masquerading as nasopharyngeal cancer.琥珀酸脱氢酶 B 突变所致多发性副神经节瘤综合征 4 型：以鼻咽癌为表现的颅底副神经节瘤的诊断和治疗挑战。
Endocr Pract. 2010 May-Jun;16(3):452-8. doi: 10.4158/EP09315.CR.
4
SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes.颈动脉体副神经节瘤中的SDHB基因突变：病例报告及副神经节瘤综合征综述
Ann Vasc Surg. 2014 Jul;28(5):1321.e9-12. doi: 10.1016/j.avsg.2013.12.012. Epub 2014 Feb 5.
5
Management of Multiple Secreting Paragangliomas in a Succinate Dehydrogenase Subunit D (SDHD) Variant Carrier.SDHD 变异携带者中多发性分泌型副神经节瘤的治疗。
Ann Thorac Surg. 2020 Feb;109(2):e87-e90. doi: 10.1016/j.athoracsur.2019.05.037. Epub 2019 Jul 4.
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Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: a founder effect?第二个中国家系中因SDHD M1I突变导致的遗传性副神经节瘤：奠基者效应？
Laryngoscope. 2003 Jun;113(6):1055-8. doi: 10.1097/00005537-200306000-00026.
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[Co-existence of nasopharyngeal carcinoma and sinonasal paraganglioma: a case report].
Kulak Burun Bogaz Ihtis Derg. 2011 Sep-Oct;21(5):298-302. doi: 10.5606/kbbihtisas.2011.046.
8
[From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].[从基因到疾病；从呼吸链缺陷基因SDHD到副神经节瘤和嗜铬细胞瘤]
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The Differential Diagnosis of Sinonasal/Nasopharyngeal Neuroendocrine/Neuroectodermally Derived Tumors.鼻窦/鼻咽神经内分泌/神经外胚层来源肿瘤的鉴别诊断
Arch Pathol Lab Med. 2015 Dec;139(12):1498-507. doi: 10.5858/arpa.2014-0383-RA.
10
High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.无症状 SDHD 和 SDHB 基因突变携带者中隐匿性副神经节瘤的高发生率。
Eur J Hum Genet. 2013 Apr;21(4):469-70. doi: 10.1038/ejhg.2012.203. Epub 2012 Sep 5.

引用本文的文献

1
Nasal Cavity Paraganglioma: Literature Review and Discussion of a Rare Case.鼻腔副神经节瘤：文献综述及1例罕见病例讨论
Biomed Hub. 2017 May 20;2(2):1-15. doi: 10.1159/000464099. eCollection 2017 May-Aug.
2
Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients.琥珀酸脱氢酶（SDH）缺陷型肾癌：一种形态学上独特的实体：来自27例患者的36个肿瘤的临床病理系列研究
Am J Surg Pathol. 2014 Dec;38(12):1588-602. doi: 10.1097/PAS.0000000000000292.
3
Reticular and myxoid non-keratinizing nasopharyngeal carcinoma: an unusual case mimicking a salivary gland carcinoma.网状和黏液样非角化鼻咽癌：一例酷似唾液腺癌的罕见病例。
Head Neck Pathol. 2014;8(3):364-8. doi: 10.1007/s12105-013-0512-6. Epub 2013 Dec 10.
4
Paucilymphoid non-keratinizing nasopharyngeal carcinoma with prominent stromal desmoplasia--an unusual case reported with brief comments on uncommon histological variants.少淋巴细胞性非角化性鼻咽癌伴显著间质纤维组织增生——报告1例罕见病例并对不常见组织学变异作简要评论
Int J Clin Exp Pathol. 2011 Apr;4(4):410-5. Epub 2011 Apr 3.

本文引用的文献

1
A case of familial paraganglioma syndrome type 4 caused by a mutation in the SDHB gene.一例由SDHB基因突变引起的4型家族性副神经节瘤综合征病例。
Nat Clin Pract Endocrinol Metab. 2006 Dec;2(12):702-6; quiz following 706. doi: 10.1038/ncpendmet0342.
2
Tumours of familial origin in the head and neck.头颈部的家族性起源肿瘤。
Oral Oncol. 2006 Nov;42(10):965-78. doi: 10.1016/j.oraloncology.2006.03.002. Epub 2006 Jul 20.
3
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.嗜铬细胞瘤/副神经节瘤综合征的临床表现及外显率
J Clin Endocrinol Metab. 2006 Mar;91(3):827-36. doi: 10.1210/jc.2005-1862. Epub 2005 Nov 29.
4
Genetic testing in pheochromocytoma or functional paraganglioma.嗜铬细胞瘤或功能性副神经节瘤的基因检测
J Clin Oncol. 2005 Dec 1;23(34):8812-8. doi: 10.1200/JCO.2005.03.1484.
5
Paraganglioma of the nasal cavity: a case report.鼻腔副神经节瘤：一例报告
Eur Arch Otorhinolaryngol. 2003 Jul;260(6):336-40. doi: 10.1007/s00405-002-0569-4. Epub 2003 Jan 21.
6
Management of sarcomas of the head and neck in adults.成人头颈部肉瘤的管理
Oral Oncol. 2003 Jan;39(1):2-12. doi: 10.1016/s1368-8375(02)00032-5.
7
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.琥珀酸脱氢酶亚基SDHB中的基因突变会导致家族性嗜铬细胞瘤和家族性副神经节瘤易感性增加。
Am J Hum Genet. 2001 Jul;69(1):49-54. doi: 10.1086/321282. Epub 2001 Jun 12.
8
Biologic characteristics of paragangliomas of the nasal cavity and paranasal sinuses.鼻腔及鼻窦副神经节瘤的生物学特性
Am J Rhinol. 2000 Nov-Dec;14(6):419-26. doi: 10.2500/105065800779954284.
9
Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management.家族性副神经节瘤：分子遗传学对评估和管理的新影响
Am J Otol. 1999 Sep;20(5):639-43.
10
Familial carotid body tumors: case report and epidemiologic review.家族性颈动脉体瘤：病例报告与流行病学综述。
Cancer. 1980 Nov 1;46(9):2116-22. doi: 10.1002/1097-0142(19801101)46:9<2116::aid-cncr2820460934>3.0.co;2-s.

鼻咽部遗传性副神经节瘤

Hereditary paraganglioma of the nasopharynx.

作者信息

Said-Al-Naief Nasser, Ojha Junu

机构信息

School of Medicine, University of Alabama at Birmingham, 3556 North Pavilion 1802 6th Ave South, Birmingham, AL 35249-7331, USA.

出版信息

Head Neck Pathol. 2008 Dec;2(4):272-8. doi: 10.1007/s12105-008-0090-1. Epub 2008 Nov 9.

DOI:10.1007/s12105-008-0090-1
PMID:20614293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2807586/
Abstract

Head and neck paragangliomas are rare neuroendocrine tumors derived from neural crest cells of parasympathetic ganglia or the widely dispersed neuroendocrine cells of the head and neck region. Paragangliomas of the sinonasal tract and nasopharynx are rare. The clinicopathologic features of this unique example of a hereditary, nasopharyngeal paraganglioma, and selective entities that are included in its differential diagnosis are presented.

摘要

头颈部副神经节瘤是一种罕见的神经内分泌肿瘤，起源于副交感神经节的神经嵴细胞或头颈部广泛分布的神经内分泌细胞。鼻窦和鼻咽部的副神经节瘤较为罕见。本文介绍了这种遗传性鼻咽部副神经节瘤独特病例的临床病理特征，以及其鉴别诊断中所包含的特定实体。