多发性骨髓瘤的脊髓硬膜内病变表现:说明性病例和文献的系统回顾。

Surgical neurology international Pub Date : 2025-06-20 eCollection Date: 2025-01-01 DOI:10.25259/SNI_249_2025
Kiana Yang Prather, Beste Gülsuna, Kishore Balasubramanian, Hakeem J Shakir, Xiaochun Zhao, Chao Li
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引用次数: 0

摘要

背景:多发性骨髓瘤(MM)通常影响骨髓。当它扩散到中枢神经系统时,通常表现为颅内转移或脊髓硬膜外病变。脊髓硬膜内转移极为罕见。病例描述:53岁男性,患有免疫球蛋白A kappa MM,表现为T3-4位增强病变,包括硬膜内病变和硬膜外病变,延伸至椎间孔。病变特征提示为神经鞘瘤,但考虑到患者的病史,怀疑累及MM。手术切除和脊柱稳定,病理检查证实为浆细胞肿瘤。系统回顾了10例硬膜内脊髓病变与MM或孤立浆细胞瘤相关的文献。大多数病变位于硬膜内髓外,主要位于胸椎。治疗通常包括手术、化疗和放疗,但预后仍然很差,特别是脑膜轻扩散。结论:本病例突出了脊髓硬膜内MM受累的诊断和治疗挑战。虽然手术可以缓解症状并确认诊断,但需要密切监测脑膜扩散的风险。多学科方法对于管理这些罕见和复杂的病例至关重要,需要进一步的研究来完善治疗策略并改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spinal intradural lesion as manifestation of multiple myeloma: Illustrative case and systematic review of literature.

Background: Multiple myeloma (MM) typically affects the bone marrow. When it spreads to the central nervous system, it usually presents as intracranial metastasis or extradural spinal lesions. Intradural spinal cord metastases are exceedingly rare.

Case description: A 53-year-old male with immunoglobulin A kappa MM presented with a contrast-enhancing lesion at the T3-4 level, consisting of an intradural lesion and an extradural lesion extending through the foramen. The lesion's characteristics suggested a schwannoma, but MM involvement was suspected given the patient's history. Surgical resection and spinal stabilization were performed, and pathological examination confirmed a plasma cell neoplasm. A systematic review of the literature identified 10 cases of intradural spinal lesions associated with MM or solitary plasmacytoma. Most lesions were intradural extramedullary, located primarily in the thoracic spine. Management often included surgery, chemotherapy, and radiotherapy, but the prognosis remained poor, especially with leptomeningeal spread.

Conclusion: This case highlights the diagnostic and therapeutic challenges of intradural spinal MM involvement. While surgery can provide symptomatic relief and confirm the diagnosis, the risk of leptomeningeal dissemination requires close monitoring. A multidisciplinary approach is essential for managing these rare and complex cases, and further studies are needed to refine treatment strategies and improve patient outcomes.

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