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病例报告:异柠檬酸脱氢酶(IDH)突变、1p/19q共缺失少突胶质细胞瘤的脊髓播散性转移

Case report: Spinal drop metastasis of IDH-mutant, 1p/19q-codeleted oligodendroglioma.

作者信息

Karaman Ahmet Kursat, Korkmazer Bora, Urganci Nil, Baş Gülçin, Arslan Serdar, Comunoglu Nil, Hanci Mehmet Murat, Kızılkılıç Osman

机构信息

Department of Radiology, Sureyyapasa Chest Diseases and Thoracic Surgery Training Hospital, Istanbul, Turkey.

Division of Neuroradiology, Department of Radiology, Istanbul University-Cerrahpasa, Istanbul, Turkey.

出版信息

Front Neurol. 2022 Dec 16;13:1086591. doi: 10.3389/fneur.2022.1086591. eCollection 2022.

Abstract

BACKGROUND

Symptomatic spinal metastases of oligodendroglioma are rare. Moreover, none of the previously published cases demonstrated the typical IDH mutation and 1p/19q-codeletion for this glial tumor. This case presents an IDH mutant, 1p/19q-codeleted oligodendroglioma with multiple spinal drop metastases.

CASE DESCRIPTION

We report a case of a 55-year-old woman with left frontal grade 3 oligodendroglioma diagnosed 3 years ago. No tumor recurrence was observed in post-operative follow-up MRI examinations. However, she was admitted to our institution again with severe low back pain. Gadolinium enhanced MRI of the spine revealed an intradural, extramedullary metastatic lesion between T11-L1 levels and multiple enhancing metastatic tumor deposits around cauda equine roots between L4-S1. T11-T12 midline laminectomy was performed and gross total resection of metastatic lesions was achieved. Final histological diagnosis of the spinal lesions was WHO Grade 3 Oligodendroglioma, IDH-mutant, 1p/19q-codeleted.

CONCLUSION

This case is the first molecularly-defined spinal metastatic oligodendroglioma. The possibility of drop metastasis should be kept in mind in oligodendroglioma patients with spinal cord-related symptoms. There is no standard approach for the diagnosis and treatment of spinal metastases of this type of glial tumor.

摘要

背景

少突胶质细胞瘤的有症状脊髓转移罕见。此外,既往发表的病例均未显示出这种胶质肿瘤典型的异柠檬酸脱氢酶(IDH)突变和1p/19q共缺失。本病例呈现1例伴有多发脊髓播散转移的IDH突变、1p/19q共缺失的少突胶质细胞瘤。

病例描述

我们报告1例55岁女性,3年前被诊断为左侧额叶3级少突胶质细胞瘤。术后随访的磁共振成像(MRI)检查未观察到肿瘤复发。然而,她因严重的腰背痛再次入住我院。脊柱钆增强MRI显示在T11-L1水平有1个硬脊膜内、髓外转移灶,在L4-S1之间马尾神经根周围有多个强化的转移瘤灶。进行了T11-T12中线椎板切除术,并实现了转移灶的大体全切。脊髓病变的最终组织学诊断为世界卫生组织3级少突胶质细胞瘤,IDH突变型,1p/19q共缺失型。

结论

本病例是首例分子定义的脊髓转移性少突胶质细胞瘤。对于有脊髓相关症状的少突胶质细胞瘤患者,应牢记发生播散转移的可能性。对于这类胶质肿瘤的脊髓转移,目前尚无标准的诊断和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ddb/9800869/b592db2a31a7/fneur-13-1086591-g0001.jpg

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