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脊髓软脑膜寡树突胶质细胞瘤在脑间变性少突胶质细胞瘤切除术后伴 1p19q 共缺失 - 一例报告。

Spinal leptomeningeal oligodendrogliomatosis after resection of cerebral anaplastic oligodendoglioma with 1p19q Co-deletion - A case report.

机构信息

Department of Neurosurgery, Wellington Regional Hospital, Wellington, New Zealand.

Department of Pathology, Waikato Hospital, Hamilton, New Zealand.

出版信息

J Clin Neurosci. 2020 Mar;73:314-316. doi: 10.1016/j.jocn.2020.01.017. Epub 2020 Jan 29.

Abstract

Anaplastic Oligodendroglioma has a better prognosis in the presence of 1p19q co-deletion and IDH-1 mutation but spinal leptomeningeal dissemination of cerebral anaplastic oligodendroglioma is a rare occurrence. We describe the case of a 47 year old man with spinal leptomeningeal dissemination eight months after resection of an anaplastic cerebral oligodendroglioma presenting with encephalitic features. We present the radiological, biochemical, intraoperative and histological features of this syndrome. Despite resolution of symptoms with corticosteroid treatment and favourable biochemical markers, prognosis remains poor when spinal leptomeningeal disease is present.

摘要

间变性少突胶质细胞瘤在存在 1p19q 共缺失和 IDH-1 突变的情况下预后较好,但脑间变性少突胶质细胞瘤的脊髓软脑膜播散是一种罕见的情况。我们描述了一例 47 岁男性的病例,该患者在切除脑间变性少突胶质细胞瘤 8 个月后出现脊髓软脑膜播散,表现为脑炎特征。我们介绍了这种综合征的放射学、生化、术中和组织学特征。尽管使用皮质类固醇治疗和生化标志物改善后症状缓解,但当存在脊髓软脑膜疾病时,预后仍然较差。

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