颅内奥德赛:小儿神经节神经瘤起源于三叉神经节:一个病例报告和文献回顾。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2024-12-18 DOI:10.1186/s13256-024-04947-9
Kaveh Ebrahimzadeh, Mohammad Mirahmadi Eraghi, Farahnaz Bidari Zerehpoosh, Hesameddin Hoseini Tavasol, Mahkameh Abbaszdeh, Adam A Dmytriw, Fatemeh Jahanshahi
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引用次数: 0

摘要

背景:神经节神经瘤是一种罕见的良性肿瘤,起源于交感神经,其从第五神经发展是罕见的实体。文献中很少讨论第五神经产生的神经节神经瘤。作者描述了第二小儿神经节神经瘤起源于第五神经。病例介绍:一名7岁亚洲男性,因左侧面部感觉异常,在过去2年中伴有几次复杂的癫痫发作,来到我们诊所。病人还抱怨突然失去意识,同时向上凝视不到一分钟。脑部计算机断层扫描和磁共振成像显示一个等密度病变,包括31 × 28 mm的局灶钙化和一个从脑桥表面延伸到梅克尔洞的固体肿块,可能起源于第五神经或其根入口区。病变在t1加权序列上呈轻度低信号,在t2加权序列和流体衰减反转恢复序列上呈高信号。注射钆仅显示轻微的非均匀增强。组织病理学和免疫组化结果与神经节神经瘤一致。在神经监护下,经乙状窦后切口外侧入路及枕下侧向桥小脑角行颅脑切除术,术后平稳。结论:虽然发生于第五神经的神经节神经瘤极为罕见,但在诊断Meckel穴或桥小脑角池病变时应予以考虑。
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An intracranial odyssey: pediatric ganglioneuroma arising from the trigeminal ganglion: a case report and review of the literature.

Background: Ganglioneuroma represents an uncommon benign tumor arising from the sympathetic nerves, and its development from the fifth nerve is an infrequent entity. Few ganglioneuromas arising from the fifth nerve have been discussed in literature. The authors describe the second pediatric ganglioneuroma arising from the fifth nerve.

Case presentation: A 7 year-old Asian male suffering from left-sided facial paresthesia, accompanied by several episodes of complex seizures over the past 2 years, presented to our clinic. The patient also complained of sudden unconsciousness and concurrent upward gaze lasting less than a minute. A brain computed tomography scan and magnetic resonance imaging revealed an isodense lesion containing focal calcifications measuring 31 × 28 mm and a solid mass extending from the pontine surface to Meckel's cave, probably originating from the fifth nerve or its root entry zone. The lesion was mildly hypointense on T1-weighted sequences and hyperintense on T2-weighted and fluid attenuated inversion recovery sequences. Gadolinium injection revealed only minimal heterogeneous enhancement. Histopathologic and immunohistochemical findings were consistent with ganglioneuroma. A lateral approach via retrosigmoid incision and suboccipital lateral craniectomy toward the cerebellopontine angle was performed under neuromonitoring supervision, and the postoperative period was uneventful.

Conclusion: Although ganglioneuroma arising from the fifth nerve is an extremely rare entity, it should be considered when diagnosing lesions in Meckel's cave or the cerebellopontine angle cistern.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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