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小儿幕上节细胞神经母细胞瘤:病例报告及文献复习

Pediatric Supratentorial Ganglioneuroblastoma: Case Report and Review of Literature.

作者信息

Mirza Farhan A, Snyder Brian, Smith Vanessa D, Vasquez Raul A

机构信息

Department of Neurosurgery, University of Kentucky, Lexington, Kentucky, USA.

Department of Neurosurgery, University of Kentucky, Lexington, Kentucky, USA.

出版信息

World Neurosurg. 2018 May;113:261-266. doi: 10.1016/j.wneu.2018.02.115. Epub 2018 Feb 26.

DOI:10.1016/j.wneu.2018.02.115
PMID:29496580
Abstract

BACKGROUND

Pediatric cerebral ganglioneuroblastoma is an exceedingly rare tumor.

CASE DESCRIPTION

We describe the case of a 4-year-old boy with sudden mental status decline who was found to have a large intracranial lesion with intraventricular extension.

CONCLUSION

Management of the case and pathologic findings are discussed, along with a review of the literature on this rare entity.

摘要

背景

小儿脑神经母细胞瘤是一种极其罕见的肿瘤。

病例描述

我们描述了一名4岁男孩的病例,该男孩突然出现精神状态下降,经检查发现有一个巨大的颅内病变并向脑室内扩展。

结论

讨论了该病例的处理及病理结果,并对有关这种罕见疾病的文献进行了综述。

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引用本文的文献

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Intraventricular ganglioneuroblastoma: an uncommon location for a rare tumour in a young adult with review of literature.脑室内神经节神经母细胞瘤:一名年轻成人罕见肿瘤的不常见部位并文献复习
Int Cancer Conf J. 2024 Sep 18;14(1):12-16. doi: 10.1007/s13691-024-00726-x. eCollection 2025 Jan.
2
Primary intracranial pediatric ganglioneuroblastoma-report of two cases and review of an unusual masquerader.颅内原发性儿童节细胞神经母细胞瘤二例报告及一种不常见的伪装者的复习。
Childs Nerv Syst. 2024 Dec;40(12):4289-4294. doi: 10.1007/s00381-024-06578-3. Epub 2024 Aug 24.
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Brain and Spinal Cord Tumors of Embryonic Origin.
胚胎起源的脑和脊髓肿瘤。
Adv Exp Med Biol. 2023;1405:405-420. doi: 10.1007/978-3-031-23705-8_15.