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脊髓毛细胞型星形细胞瘤伴软脑膜播散至脑。病例报告及文献复习。

Spinal cord pilocytic astrocytoma with leptomeningeal dissemination to the brain. Case report and review of the literature.

作者信息

Abel Taylor J, Chowdhary Abhineet, Thapa Mahesh, Rutledge Joe C, Geyer J Russell, Ojemann Jeffrey, Avellino Anthony M

机构信息

Department of Neurological Surgery, Division of Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington School of Medicine, Seattle, Washington 98105, USA.

出版信息

J Neurosurg. 2006 Dec;105(6 Suppl):508-14. doi: 10.3171/ped.2006.105.6.508.

Abstract

Leptomeningeal dissemination of low-grade spinal cord gliomas is an uncommon event. The authors report a unique case of leptomeningeal dissemination of a spinal cord pilocytic astrocytoma (PCA) to the intracranial cerebral subarachnoid spaces in a child. A 2-year-old boy presented with a loss of balance and the inability to walk or stand. An intradural intramedullary spinal cord tumor was identified, and the lesion was subtotally resected and diagnosed by the pathology department to be a PCA. Subsequently, the patient had recurrences of the intradural intramedullary tumor at 6 months and 2 years after his original presentation. He underwent a repeated resection of the recurrent tumor and fenestration of an associated syrinx on both occasions. The pathological characteristics of the reresected tumor remained consistent with those of a PCA. Postoperative imaging after his last surgery revealed diffuse intracranial leptomeningeal dissemination into the cisternal space surrounding the midbrain, the suprasellar region, and the internal auditory canal, as well as nodular subarachnoid disease in the upper cervical region. The patient then underwent chemotherapy, and total spine magnetic resonance (MR) imaging 2 months later demonstrated stability in the size of the spinal cord tumor and a decrease in the associated syrinx. However, an MR image of the head demonstrated two new areas of supratentorial subarachnoid leptomeningeal spread of the primary spinal cord tumor at the 2-month follow-up examination. At the 6-month follow-up examination, MR imaging of the head and spine demonstrated stable metastatic disease. This case illustrates a unique instance of supratentorial leptomeningeal dissemination of an intramedullary spinal cord PCA in a child.

摘要

低级别的脊髓胶质瘤软脑膜播散是一种罕见的情况。作者报告了一例独特的病例,一名儿童脊髓毛细胞型星形细胞瘤(PCA)发生软脑膜播散至颅内脑蛛网膜下腔。一名2岁男孩出现平衡能力丧失,无法行走或站立。经检查发现硬脊膜内髓内脊髓肿瘤,病变部分切除,病理科诊断为PCA。随后,患者在初次就诊后6个月和2年时硬脊膜内髓内肿瘤复发。他在这两次复发时均接受了复发性肿瘤的再次切除及相关脊髓空洞症的开窗手术。再次切除肿瘤的病理特征与PCA一致。他最后一次手术后的影像学检查显示,颅内软脑膜弥漫性播散至中脑周围脑池间隙、鞍上区域和内耳道,以及上颈部蛛网膜下腔结节状病变。该患者随后接受了化疗,2个月后的全脊柱磁共振(MR)成像显示脊髓肿瘤大小稳定,相关脊髓空洞症缩小。然而,在2个月的随访检查中,头部MR图像显示原发性脊髓肿瘤在幕上蛛网膜下腔软脑膜播散出现两个新区域。在6个月的随访检查中,头部和脊柱的MR成像显示转移性疾病稳定。该病例说明了儿童髓内脊髓PCA幕上软脑膜播散的一个独特实例。

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