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一名4岁女童舌下神经咽旁神经节瘤:一例罕见病例报告

Parapharyngeal ganglioneuroma of hypoglossal nerve in a 4 year old girl: a rare case report.

作者信息

Hallur Neelakamal, Sikkerimath B C, Gudi Santhosh S, Chour Girish, Ginimav Sneha, Nidoni Madhumati

机构信息

Department of Oral and Maxillofacial Surgery, PMNM Dental College and Hospital, Bagalkot, Karnataka India.

出版信息

J Maxillofac Oral Surg. 2012 Sep;11(3):343-6. doi: 10.1007/s12663-011-0192-2. Epub 2011 May 6.

DOI:10.1007/s12663-011-0192-2
PMID:23997490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428456/
Abstract

Parapharyngeal ganglioneuroma of hypoglossal nerve is very rare benign tumor arising from sympathetic nervous system producing mass and functional effect. We present a rare case in 4 year old girl with history of swelling and odynophagia in left side of neck. Extensive clinical, immunohistochemistry, and imaging of the swelling confirmed the diagnosis of ganglioneuroma after surgical excision.

摘要

舌下神经咽旁神经节瘤是一种非常罕见的良性肿瘤,起源于交感神经系统,可产生肿块和功能影响。我们报告了一例罕见病例,患者为一名4岁女孩,有左侧颈部肿胀和吞咽痛病史。对该肿胀进行了全面的临床、免疫组织化学和影像学检查,手术切除后确诊为神经节瘤。

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Sporadic synchronous ganglioneuromas in a child--case report and review.儿童散发性同步节细胞神经瘤——病例报告并文献复习
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Ganglioneuroma of adrenal gland in a patient with Turner syndrome.患者特纳综合征合并肾上腺节细胞神经瘤。
Ann Diagn Pathol. 2010 Apr;14(2):133-6. doi: 10.1016/j.anndiagpath.2009.06.007. Epub 2009 Sep 8.
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Ganglioneuroma of the mandible resulting from metastasis of neuroblastoma.神经母细胞瘤转移导致的下颌骨神经节细胞瘤。
Int J Oral Maxillofac Surg. 2009 Feb;38(2):196-8. doi: 10.1016/j.ijom.2008.09.009. Epub 2008 Nov 18.
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A 5-year-old girl with a congenital ganglioneuroma diagnosed by fine needle aspiration biopsy: a case report.一名通过细针穿刺活检确诊为先天性神经节神经瘤的5岁女孩:病例报告。
Cytojournal. 2008 Mar 30;5:5. doi: 10.1186/1742-6413-5-5.
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