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Glomus vagale tumour, can it be diagnosed only on sonography?迷走神经球瘤,仅通过超声检查就能诊断吗?
J Ultrasound. 2017 Jan 13;20(1):73-79. doi: 10.1007/s40477-016-0237-y. eCollection 2017 Mar.
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[Glomus tumors of the head-neck-region].[头颈部区域的血管球瘤]
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Chemodectomas (nonchromaffin paragangliomas) of the glomus jugulare, glomus vagale and carotid body.颈静脉球、迷走神经球和颈动脉体的化学感受器瘤(非嗜铬性副神经节瘤)
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本文引用的文献

1
Neck schwannoma diagnosed by core needle biopsy: a case report.经粗针活检诊断的颈部神经鞘瘤:一例报告
J Ultrasound. 2014 Jul 1;18(4):407-10. doi: 10.1007/s40477-014-0112-7. eCollection 2015 Dec.
2
Branchial cleft cyst.鳃裂囊肿
J Ultrasound. 2013 Mar 1;16(1):17-20. doi: 10.1007/s40477-013-0004-2. eCollection 2013.
3
Role of ultrasound and color Doppler imaging in the detection of carotid paragangliomas.超声及彩色多普勒成像在颈动脉体瘤检测中的作用
J Ultrasound. 2012 Sep;15(3):158-63. doi: 10.1016/j.jus.2012.05.001. Epub 2012 May 30.
4
Vagal paragangliomas: two case reports.迷走神经副神经节瘤:两例病例报告。
Acta Otorhinolaryngol Ital. 2007 Jun;27(3):139-43.
5
Cervical sympathetic chain schwannoma: two different clinical presentations.颈交感神经链神经鞘瘤:两种不同的临床表现。
Tumori. 2007 May-Jun;93(3):305-7. doi: 10.1177/030089160709300316.
6
Bilateral Abnormal Relationship of the Vagus Nerve in its Cervical Portion.迷走神经颈段的双侧异常关系。
J Anat Physiol. 1915 Jul;49(Pt 4):389-92.
7
Secreting vagal paraganglioma.分泌型迷走神经副神经节瘤
Am J Otolaryngol. 2004 Jul-Aug;25(4):295-300. doi: 10.1016/j.amjoto.2004.02.007.
8
The vagal body and its tumour.迷走神经体及其肿瘤。
Aust N Z J Surg. 1953 Aug;23(1):48-54. doi: 10.1111/j.1445-2197.1953.tb05016.x.
9
High-resolution sonography of lower extremity peripheral nerves: anatomic correlation and spectrum of disease.下肢周围神经的高分辨率超声检查:解剖学关联及疾病谱
J Ultrasound Med. 2002 Mar;21(3):315-22. doi: 10.7863/jum.2002.21.3.315.
10
Cervical paragangliomas: diagnosis, management and complications.颈副神经节瘤:诊断、治疗及并发症
J Laryngol Otol. 2001 Jun;115(6):467-74. doi: 10.1258/0022215011908180.

迷走神经球瘤,仅通过超声检查就能诊断吗?

Glomus vagale tumour, can it be diagnosed only on sonography?

作者信息

Bhatt Shuchi, Verma Pooja, Meena Neha, Tandon Anupama, Tanveer Nadeem, Bansal Divya

机构信息

Department of Radio-diagnosis, University College of Medical sciences (University of Delhi) and GTB Hospital, Dilshad Garden, Delhi, 110095 India.

Department of Pathology, University College of Medical Sciences (University of Delhi) and GTB Hospital, Dilshad Garden, Delhi, 110095 India.

出版信息

J Ultrasound. 2017 Jan 13;20(1):73-79. doi: 10.1007/s40477-016-0237-y. eCollection 2017 Mar.

DOI:10.1007/s40477-016-0237-y
PMID:28298947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5334275/
Abstract

Vagal paragangliomas are rare benign tumors accounting for only 3% of head and neck paragangliomas and arise from vagal ganglions, predominately the nodose ganglion in the carotid sheath. Imaging plays an important role in their diagnosis, differentiation from more common lesions presenting in the carotid space, and management. MRI is the method of choice for investigation when paragangliomas are clinically suspected. The typical salt-and-pepper appearance in T1-weighted images is well known but not specific to paragangliomas. Demonstration of the continuity of the lesion with the vagus nerve on magnetic resonance imaging (MRI) further asserts the diagnosis of glomus vagale. Although this tumor can be diagnosed on a contrast-enhanced computed tomography (CECT) examination, it is limited by the non-demonstration of its neural origin. Sonography is considered only a preliminary investigation in patients, and a CECT and/or MRI study of the neck is conducted before treatment planning. This case is unique as a confident diagnosis of glomus vagale was made on high-resolution sonography of the neck. A middle-aged male patient presenting with a neck swelling was diagnosed with a glomus vagale tumor on USG by the direct demonstration of its continuity with the vagus nerve, and Doppler examination confirmed its vascularity. The diagnosis was confirmed on histopathology after surgical excision. The sonographic appearance, Doppler characteristics, and imaging differential diagnosis of glomus vagale are discussed in detail.

摘要

迷走神经副神经节瘤是罕见的良性肿瘤,仅占头颈部副神经节瘤的3%,起源于迷走神经节,主要是颈动脉鞘内的结节状神经节。影像学在其诊断、与颈动脉间隙更常见病变的鉴别以及治疗中起着重要作用。当临床怀疑有副神经节瘤时,MRI是首选的检查方法。T1加权图像上典型的“椒盐”样表现广为人知,但并非副神经节瘤所特有。磁共振成像(MRI)显示病变与迷走神经的连续性进一步支持了迷走神经球瘤的诊断。虽然这种肿瘤可通过增强计算机断层扫描(CECT)检查诊断,但它受限于无法显示其神经起源。超声检查仅被视为对患者的初步检查,在制定治疗计划前需对颈部进行CECT和/或MRI检查。该病例独特之处在于通过颈部高分辨率超声检查确诊了迷走神经球瘤。一名出现颈部肿胀的中年男性患者,通过超声直接显示病变与迷走神经的连续性而被诊断为迷走神经球瘤,多普勒检查证实了其血管情况。手术切除后经组织病理学确诊。本文详细讨论了迷走神经球瘤的超声表现、多普勒特征及影像学鉴别诊断。