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先前接受根治性治疗的颞叶多形性胶质母细胞瘤在无颅内复发情况下的脊髓硬膜内髓内播散

Spinal Intradural Intramedullary Dissemination in the Absence of Intracranial Relapse of a Previously Radically Treated Temporal Lobe Glioblastoma Multiforme.

作者信息

Serrano Lucas, Archavlis Eleftherios, Januschek Elke, Timofeev Pavel, Ulrich Peter

机构信息

aDepartment of Neurosurgery, Mainz University Hospital, Mainz, Germany.

bDepartment of Neurosurgery, Sana Klinikum Offenbach, Offenbach, Germany.

出版信息

Case Rep Oncol. 2017 Mar 29;10(1):281-289. doi: 10.1159/000464279. eCollection 2017 Jan-Apr.

Abstract

Intracranial glioblastoma multiforme (GBM) constitutes the most frequent and unfortunately aggressive primary central nervous system malignancy. Despite the high tendency of these tumors to show local relapse within the brain after primary therapy, dissemination into the spinal axis is an infrequent event. If spinal metastases occur they are leptomeningeal in the vast majority of cases and always in the context of intracranial progressive disease. Spinal intramedullary metastases of intracranial GBM have rarely been described to date. We report the unique case of a young woman with subacute progressive paraparesis due to spinal intramedullary metastases of a temporal lobe GBM despite the remarkable absence of intracranial tumor relapse. The patient had undergone gross total resection of a left temporal GBM in contact with the ventricles and cisternal space followed by radio- and chemotherapy 13 months before. At the moment of diagnosis of spinal intramedullary metastases, there were no signs of intracranial tumor recurrence as revealed by MRI scans. Since a high level of suspicion may be needed to detect this rare evolution of intracranial GBM and other differential diagnoses must be ruled out at presentation, we discuss the important features of this case regarding clinical manifestation, diagnosis, surgery, and management. Furthermore, we mention possible factors that may have contributed to the development of these metastases in the context of intracranial remission.

摘要

颅内多形性胶质母细胞瘤(GBM)是最常见且不幸的是侵袭性最强的原发性中枢神经系统恶性肿瘤。尽管这些肿瘤在初次治疗后在脑内局部复发的倾向很高,但播散至脊髓轴是罕见事件。如果发生脊髓转移,绝大多数情况下是软脑膜转移,且总是在颅内疾病进展的背景下发生。颅内GBM的脊髓髓内转移迄今为止很少被描述。我们报告了一例独特的病例,一名年轻女性因颞叶GBM的脊髓髓内转移出现亚急性进行性截瘫,尽管颅内肿瘤明显未复发。患者在13个月前接受了与脑室和脑池空间相邻的左颞叶GBM的全切手术,随后进行了放疗和化疗。在诊断脊髓髓内转移时,MRI扫描显示没有颅内肿瘤复发的迹象。由于可能需要高度怀疑才能检测到颅内GBM的这种罕见演变,且在就诊时必须排除其他鉴别诊断,我们讨论了该病例在临床表现、诊断、手术和治疗方面的重要特征。此外,我们提到了在颅内缓解的情况下可能促成这些转移发生的潜在因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1278/5422745/d95704922b1b/cro-0010-0281-g01.jpg

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