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终丝室管膜瘤伴囊性形成:病例报告及文献复习。

Subependymoma of the Conus Medullaris with Cystic Formation: Case Report and a Literature Review.

机构信息

Department of Neurosurgery, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

Department of Neurosurgery, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

出版信息

World Neurosurg. 2020 May;137:235-238. doi: 10.1016/j.wneu.2020.02.053. Epub 2020 Feb 17.

Abstract

BACKGROUND

Subependymoma in the spinal cord is very rare and usually occurs in the cervical cord. We report an exceptional case of subependymoma that occurred at the conus medullaris with cystic formation. This article reviews the literature on subependymoma in the conus medullaris; discusses its clinical manifestations, imaging findings, and differential diagnoses; and offers an opinion about the cystic formation of the subependymoma.

CASE DESCRIPTION

A 69-year-old woman experienced progressive limb weakness with a somatosensory abnormality for 3 months. Preoperative magnetic resonance imaging showed a cystic intramedullary lesion at the conus medullaris with a well-defined margin. A preliminary diagnosis of epidermoid cyst was made based on the imaging findings. During the operation, cystic formation of the tumor was found, and the tumor was completely removed. Pathology showed an uneven proliferation of glial cells, consistent with subependymal morphology, and the tumor was confirmed as subependymoma.

CONCLUSIONS

We present an extremely rare case of cystic formation in subependymoma at the conus medullaris. Subependymoma should be included in the differential diagnosis of intramedullary cystic lesions. The breakdown of the blood-brain barrier and excessive extravasation may be potential mechanisms of cystic formation.

摘要

背景

脊髓室管膜下瘤非常罕见,通常发生在颈髓。我们报告一例罕见的发生在终丝部位的伴有囊性形成的室管膜下瘤病例。本文回顾了终丝部位室管膜下瘤的文献;讨论了其临床表现、影像学表现和鉴别诊断;并对室管膜下瘤的囊性形成提出了看法。

病例描述

一名 69 岁女性因进行性四肢无力伴感觉异常 3 个月就诊。术前磁共振成像显示终丝部位有一个边界清楚的囊性髓内病变。根据影像学表现初步诊断为表皮样囊肿。术中发现肿瘤囊性形成,肿瘤被完全切除。病理显示神经胶质细胞不均匀增生,符合室管膜下形态,肿瘤被确诊为室管膜下瘤。

结论

我们报告了一例极其罕见的终丝部位伴有囊性形成的室管膜下瘤病例。室管膜下瘤应纳入髓内囊性病变的鉴别诊断。血脑屏障的破坏和过度渗出可能是囊性形成的潜在机制。

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