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中枢神经轴的颅底钙化假性肿瘤:两例病例报告和文献系统回顾。

Skull Base Calcifying Pseudoneoplasms of the Neuraxis: Two Case Reports and a Systematic Review of the Literature.

机构信息

Division of Neurosurgery, McMaster University, Hamilton, Ontario, Canada.

Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Can J Neurol Sci. 2020 May;47(3):389-397. doi: 10.1017/cjn.2019.339.

Abstract

BACKGROUND

Calcifying pseudoneoplasm of the neuraxis (CAPNON) is a rare tumefactive lesion. CAPNONs can mimic calcified meningiomas at the skull base.

METHODS

Here, we report two cases of CAPNON and present a systematic review of the literature on skull base CAPNONs, to compare CAPNONs with calcified meningiomas.

RESULTS

Case 1: A 57-year-old man presented with right-sided lower cranial neuropathies and gait ataxia. He underwent a subtotal resection of a right cerebellopontine angle lesion, with significant improvement of his gait ataxia. However, his cranial neuropathies persisted. Pathological examination of the lesion was diagnostic of CAPNON, with the entrapped nerve fibers identified at the periphery of the lesion, correlating with the patient's cranial neuropathy. Case 2: A 70-year-old man presented with progressive headache, gait difficulty, and cognitive impairment. He underwent a frontotemporal craniotomy for a near-total resection of his right basal frontal CAPNON. He remained neurologically stable 7 years after the initial resection without evidence of disease recurrence. We analyzed 24 reported CAPNONs at the skull base in our systematic review of the literature. Cranial neuropathies were present in 11 (45.8%) patients. Outcomes regarding cranial neuropathies were documented in six patients: two had sacrifice of the nerve function with surgical approaches and four had persistent cranial neuropathies.

CONCLUSION

While CAPNON can radiologically and grossly mimic calcified meningiomas, they are two distinctly different pathologies. CAPNONs located at the skull base are commonly associated with cranial neuropathies, which may be difficult to reverse despite surgical intervention.

摘要

背景

中枢神经系统钙化假性肿瘤(CAPNON)是一种罕见的肿块样病变。CAPNON 可在颅底模拟为钙化脑膜瘤。

方法

在此,我们报告两例 CAPNON 病例,并对颅底 CAPNON 进行文献系统回顾,以将 CAPNON 与钙化脑膜瘤进行比较。

结果

病例 1:一名 57 岁男性表现为右侧颅神经病变和步态共济失调。他接受了右侧桥小脑角病变的次全切除术,步态共济失调明显改善。然而,他的颅神经病变仍然存在。病变的病理检查诊断为 CAPNON,病变外周的受困神经纤维与患者的颅神经病变相关。病例 2:一名 70 岁男性表现为进行性头痛、步态困难和认知障碍。他接受了额颞部开颅术,对其右侧基底额部 CAPNON 进行了近全切除术。在初始切除后 7 年,他仍然保持神经稳定,没有疾病复发的迹象。我们在文献系统回顾中分析了 24 例颅底 CAPNON。11 例(45.8%)患者存在颅神经病变。6 例患者记录了颅神经病变的结果:2 例因手术方法导致神经功能丧失,4 例持续存在颅神经病变。

结论

虽然 CAPNON 在影像学和大体上可能与钙化脑膜瘤相似,但它们是两种截然不同的病理类型。位于颅底的 CAPNON 通常与颅神经病变相关,尽管进行了手术干预,但这些病变可能难以逆转。

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