复发性颅内间变性脑膜瘤的颈椎转移:说明性病例。

Grimi Alessandro, Mario De Robertis, Ali Baram, Gabriele Capo, Elena Clerici, Bethania Fernandes, Marco Riva, Federico Pessina, Carlo Brembilla, Maurizio Fornari
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引用次数: 0

摘要

背景:脑膜瘤是最常见的中枢神经系统原发肿瘤,大多数归类为良性(WHO分级I级),预后良好。然而,一小部分脑膜瘤表现出恶性行为,以局部侵袭和远处转移为特征,发生在不到1%的病例中。转移性脑膜瘤最常累及肺、骨、肝和软组织,骨转移给诊断和治疗带来重大挑战。观察:一位61岁男性,有复发性颅内脑膜瘤病史,表现为颈部疼痛和指感异常。影像学检查显示C4和C5椎骨病变,并伴有C5椎骨病理性骨折。因此,行C4和C5椎体切除术并前路重建。组织分子分析证实骨内间变性脑膜瘤的存在。经验教训:转移性脑膜瘤是一种罕见的实体,需要多学科的方法来准确检测和有效的管理。分子和基因图谱的整合,以及先进的成像技术,可能有助于高风险肿瘤的识别,指导个性化的治疗策略,并最终改善患者的预后。https://thejns.org/doi/10.3171/CASE24863。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cervical vertebral metastases from a recurrent intracranial anaplastic meningioma: illustrative case.

Background: Meningiomas represent the most prevalent primary tumors of the central nervous system, with the majority classified as benign (WHO grade I) and exhibiting favorable prognoses. However, a rare subset of meningiomas show malignant behavior, characterized by local invasion and distant metastasis, occurring in less than 1% of cases. Metastatic meningiomas most commonly involve the lungs, bones, liver, and soft tissues, with bone metastases presenting significant diagnostic and therapeutic challenges.

Observations: A 61-year-old male with a history of recurrent intracranial meningiomas presented with neck pain and digital paresthesia. Imaging studies revealed lesions at the C4 and C5 vertebrae, accompanied by a pathological fracture at C5. Consequently, a C4 and C5 corpectomy with anterior reconstruction was performed. Histomolecular analysis confirmed the presence of an intraosseous anaplastic meningioma.

Lessons: Metastatic meningiomas are an uncommon entity that necessitates a multidisciplinary approach for accurate detection and effective management. The integration of molecular and genetic profiling, along with advanced imaging techniques, may facilitate the identification of high-risk tumors, guide personalized treatment strategies, and ultimately improve patient outcomes. https://thejns.org/doi/10.3171/CASE24863.

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