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一例具有不寻常表现的原发性鞍区嗅神经母细胞瘤:病例报告及文献复习

A primary sellar esthesioneuroblastomas with unusual presentations: a case report and reviews of literatures.

作者信息

Lin Jiann-Her, Tsai Dong-Han, Chiang Yung-Hsiao

机构信息

Department of Neurosurgery, Tri-Service General Hospital, 325, Sec. 2, Cheng-Kung Road, Neihu, Taipei 114, Taiwan, ROC.

出版信息

Pituitary. 2009;12(1):70-5. doi: 10.1007/s11102-007-0081-3.

DOI:10.1007/s11102-007-0081-3
PMID:18176843
Abstract

The development of an esthesioneuroblastoma outside to the region in which olfactory epithelium exists is extremely rare. Only nine cases were reported in the previous literatures. The author presents a 40 years-old man with ectopic esthesioneuroblastoma in sella turcica. In contrast to the previous nine cases, our case presented unusual presentations-CSF rhinorrhea and meningitis. Endoscopic transphenoid approach with removal of tumor and repair of dura defect followed by radiotherapy offered a good result in this case. Moreover, differential diagnosis and the origin of the ectopic esthsioneuroblastoma would be discussed.

摘要

嗅神经母细胞瘤发生于嗅上皮所在区域以外的情况极为罕见。既往文献仅报道过9例。作者报告了1例40岁男性,其蝶鞍区存在异位嗅神经母细胞瘤。与既往9例不同,本例表现出不寻常的症状——脑脊液鼻漏和脑膜炎。经鼻内镜蝶窦入路切除肿瘤并修复硬脑膜缺损,随后进行放射治疗,该病例取得了良好效果。此外,还将讨论异位嗅神经母细胞瘤的鉴别诊断及起源。

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Olfactory neuroblastoma: a case report and review of the literature.嗅神经母细胞瘤:一例报告并文献复习
Ear Nose Throat J. 2005 Mar;84(3):150-2.
2
Combined endoscopic surgery and radiosurgery as treatment modality for olfactory neuroblastoma (esthesioneuroblastoma).联合内镜手术和放射外科作为嗅神经母细胞瘤(嗅神经上皮瘤)的治疗方式。
Acta Neurochir (Wien). 2005 Jun;147(6):595-601; discussion 601-2. doi: 10.1007/s00701-005-0521-7. Epub 2005 Apr 11.
3
Primary sellar esthesioneuroblastoma.原发性鞍区嗅神经母细胞瘤。
Ectopic Olfactory Neuroblastoma: Systematic Review of a Rare Clinical Entity among Sinonasal Tumors.
异位嗅神经母细胞瘤:鼻窦肿瘤中一种罕见临床实体的系统评价
J Neurol Surg B Skull Base. 2023 Jan 5;85(2):109-118. doi: 10.1055/a-1993-7790. eCollection 2024 Apr.
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Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma.伪装成垂体大腺瘤的原发性鞍区神经母细胞瘤。
JCEM Case Rep. 2023 Jul 12;1(4):luad081. doi: 10.1210/jcemcr/luad081. eCollection 2023 Jul.
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