A rare case of metastatic atypical meningioma that highlights the shortcomings of treatment options at present.

IF 0.9 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Acta radiologica open Pub Date : 2022-07-05 eCollection Date: 2022-07-01 DOI:10.1177/20584601221109891
Erik Kristian Maurice Wrange, Stefan Markus Walbom Harders
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Abstract

We report a case of a locally invasive recurrent atypical meningioma in the temporal region with late onset of meningioma lung metastasis. The patient was diagnosed in early adolescence with an atypical meningioma believed to be radiotherapy induced following treatment of a benign pilocytic astrocytoma in the hypothalamus region at 6 years of age. Even though the patient underwent several surgical and radiotherapy treatments, the intracranial meningioma kept growing and was locally invasive. The patient received experimental treatment with bevacizumab, a vascular endothelial growth factor A (VEGF-A)-inhibitor, for 4 years from age 26. Treatment was withdrawn after proven tumor growth on routine control MRI. A DOTA-TOC PET-CT-scan was performed to evaluate the DOTA-TOC somatostatin receptor number for possible SSTR (somatostatin receptor targeted therapy). In the included scan plan multiple lung metastasis were detected and later verified. Genomic tumor sequencing was performed, but no targeted treatment options were found. Instead, the patient finally, as the last treatment option, underwent 4 series of SSTR-targeted therapy (Lutetium DOTA-TOC). Unfortunately, the intracranial tumor component significantly progressed during the final stages of the treatment and the patient died less than a year after treatment was withdrawn at age 32. This case story illustrates the shortcomings of atypical/anaplastic meningioma treatment strategies at present and highlights the possibility of extracranial metastasis.

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一例罕见的转移性非典型脑膜瘤,突出了目前治疗方案的缺点。
我们报告一例局部侵袭性复发性颞区非典型脑膜瘤伴晚发性脑膜瘤肺转移。患者在青春期早期被诊断为非典型脑膜瘤,据信是在6岁时下丘脑区良性毛细胞星形细胞瘤治疗后放射治疗引起的。尽管患者接受了多次手术和放疗治疗,颅内脑膜瘤仍在继续生长并局部侵袭。患者从26岁开始接受贝伐单抗(一种血管内皮生长因子a (VEGF-A)抑制剂)的实验性治疗,为期4年。常规对照MRI证实肿瘤生长后停止治疗。进行DOTA-TOC pet - ct扫描,评估DOTA-TOC生长抑素受体数量,以进行可能的SSTR(生长抑素受体靶向治疗)。在纳入的扫描计划中,发现并证实了多发肺转移。进行了肿瘤基因组测序,但没有发现靶向治疗方案。作为最后的治疗选择,患者最终接受了4个系列的sstr靶向治疗(Lutetium DOTA-TOC)。不幸的是,在治疗的最后阶段,颅内肿瘤成分明显恶化,患者在治疗结束后不到一年就死亡,享年32岁。本病例说明了目前非典型/间变性脑膜瘤治疗策略的不足,并强调了颅外转移的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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