Ganglioneuroma in The Neck Region: A Case Report

Q4 Medicine
N. Chikuie, T. Hamamoto, T. Ishino, T. Ueda, A. Nagasawa, H. Kuniyasu, Rina Fujiwara-Tani, S. Takeno
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引用次数: 1

Abstract

Ganglioneuroma, which rarely occurs in the neck region, is a well-differentiated benign tumor of the sympathetic nervous system. A 39-year-old man presented with neck swelling for a year. A giant tumor was located on the left side of the neck. Schwannoma was suspected on preoperative cytology and core needle biopsy, and the postoperative diagnosis on pathological examination was ganglioneuroma. The origin of the tumor was considered to be the sympathetic nervous system based on the postoperative appearance of Horner’s syndrome. The treatment choice for ganglioneuromas is complete surgical resection, contrary to the nerve-sparing resection of schwannomas. Therefore, making the definitive diagnosis before surgical resection could be important. In this report, we focus on the differential diagnosis obtained with radiological findings and the treatment strategy for the tumor with a literature review.
颈部神经节神经瘤1例报告
神经节神经瘤是一种分化良好的交感神经系统良性肿瘤,很少发生在颈部。一名39岁的男子出现颈部肿胀一年。颈部左侧有一个巨大的肿瘤。术前细胞学检查和核心针活检怀疑为神经鞘瘤,术后病理检查诊断为神经节神经鞘瘤。根据Horner综合征的术后表现,肿瘤的起源被认为是交感神经系统。神经节神经鞘瘤的治疗选择是完全手术切除,而不是保留神经的神经鞘瘤切除。因此,在手术切除前做出明确的诊断可能很重要。在本报告中,我们通过文献综述,重点关注放射学检查结果的鉴别诊断和肿瘤的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
CiteScore
0.30
自引率
0.00%
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