继发于神经轴钙化假瘤的眼运动压迫性神经病(CAPNON)。

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2024-10-11 eCollection Date: 2024-10-01 DOI:10.1093/jscr/rjae507
Verónica Alzate-Carvajal, Humberto Jose Madriñán-Navia, Luis Alberto Escobar, Camilo E Moreno-Huertas
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引用次数: 0

摘要

神经轴钙化性假瘤(CAPNON)是一种不常见的疾病,也是第三颅神经麻痹的罕见病因。我们回顾了一例 17 岁男性患者的病例,该患者出现进行性左侧第三颅神经麻痹 9 个月。脑磁共振图像显示左侧clinoidal病变,T2和T1序列呈低信号强度,计算机断层扫描显示有钙化迹象,血管磁共振成像显示无血管病变。对病灶进行了左翼切口,后方蝶窦切除术和全切除术。神经轴钙化性假瘤是一种不常见的病理现象,多发于颅底和脊柱,在出现压迫现象时需要手术治疗,并应考虑脑膜瘤、脊索瘤和转移瘤等鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oculomotor compressive neuropathy secondary to calcifying pseudoneoplasm of the neuraxis (CAPNON).

Calcifying pseudoneoplasm of the neuraxis (CAPNON) is an uncommon entity and a rare cause of third cranial nerve palsy. We review the case of a 17-year-old male with a 9-month history of progressive left third cranial nerve palsy. Cerebral magnetic resonance image showed a left clinoidal lesion with low signal intensity in T2 and T1 sequences with signs of calcification in the computed tomography and without vascular lesion in AngioMRI. A left pterional approach was performed with posterior clinoidectomy and total resection of the lesion. Calcifying pseudoneoplasm of the neuraxis is an infrequent pathology that presents in the skull base and spine that requires surgical treatment in the presence of compressive phenomena and differential diagnosis as meningioma, chordoma, and metastasis should be considered.

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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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