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本文引用的文献

1
Glomus jugulare tumour presenting with isolated accessory nerve palsy.以孤立性副神经麻痹为表现的颈静脉球瘤
J Laryngol Otol. 2004 Mar;118(3):234-6. doi: 10.1258/002221504322928053.
2
The glomus tumor and its biology.血管球瘤及其生物学特性。
Laryngoscope. 1993 Nov;103(11 Pt 2 Suppl 60):7-15. doi: 10.1002/lary.1993.103.s60.7.
3
Glomus tumor: a clinicopathologic and electron microscopic study.血管球瘤：一项临床病理及电子显微镜研究。
Cancer. 1982 Oct 15;50(8):1601-7. doi: 10.1002/1097-0142(19821015)50:8<1601::aid-cncr2820500823>3.0.co;2-5.
4
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.一个受基因组印记影响且与遗传性副神经节瘤相关的基因定位于染色体11q23 - qter。
Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7.

鼓室球瘤临床病程改变——病例报告

Altered clinical course of glomus tympanicum - a case report.

作者信息

Subashini P, Mohanty Sanjeev

机构信息

Department of Otolaryngology - Head and Neck Surgery, Sri Ramachandra Medical College and Research Institute, Chennai, Tamilnadu, India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2008 Mar;60(1):35-6. doi: 10.1007/s12070-008-0011-3. Epub 2008 Apr 3.

DOI:10.1007/s12070-008-0011-3
PMID:23120495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3450722/
Abstract

Glomus tumours of temporal bone are rare and usually present with symptoms of hearing loss and tinnitus. Diagnosis is often delayed due to the slow growth of the tumour. Here we present a case report of a patient diagnosed as glomus tympanicum who presented only with unilateral progressive hearing loss for the past one year and rapidly detoriating hearing loss since two months who was managed successfully.

摘要

颞骨球瘤罕见，通常表现为听力丧失和耳鸣症状。由于肿瘤生长缓慢，诊断往往延迟。本文报告一例诊断为鼓室球瘤的患者，该患者在过去一年仅表现为单侧进行性听力丧失，近两个月听力迅速恶化，经成功治疗。