神经节瘤:一种罕见的阑尾肿瘤--病例报告和文献综述。

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2024-12-16 eCollection Date: 2024-12-01 DOI:10.1093/jscr/rjae735
Rakesh Quinn, Jodie Ellis-Clark
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引用次数: 0

摘要

神经节神经瘤(Ganglioneuromas, GN)是起源于外胚层的肿瘤,起源于神经嵴细胞。阑尾GN极为罕见,当代文献中仅有8例病例报告。由于GNs是良性和惰性的,切除的必要性经常被争论。然而,获得组织以确认诊断可能具有挑战性,经常导致手术切除。我们报告一例85岁男性阑尾结节肿大的内镜诊断。进一步的计算机断层扫描未能明确病理。行腹腔镜阑尾切除术,确诊为阑尾GN。
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Ganglioneuroma: a rare appendiceal tumour - case report and literature review.

Ganglioneuromas (GN) are tumours of ectodermal origin, derived from the neural crest cells. Appendiceal GN are extremely rare, with only eight contemporary case reports in the literature. Being benign and indolent, the necessity of resection for GNs is often debated. However, obtaining tissue to confirm the diagnosis can be challenging, frequently leading to surgical resection. We present a case of an 85-year-old male with an enlarging appendiceal nodule diagnosed endoscopically. Further investigation with computed tomography (CT) scan failed to define the pathology. A laparoscopic appendicectomy was performed, which confirmed the diagnosis of appendiceal GN.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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