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脊髓硬膜内病变作为多发性骨髓瘤的表现:病例说明及文献系统综述

Spinal intradural lesion as manifestation of multiple myeloma: Illustrative case and systematic review of literature.

作者信息

Prather Kiana Yang, Gülsuna Beste, Balasubramanian Kishore, Shakir Hakeem J, Zhao Xiaochun, Li Chao

机构信息

Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, United States.

College of Medicine, Texas A&M Health Science Center, Houston, United States.

出版信息

Surg Neurol Int. 2025 Jun 20;16:247. doi: 10.25259/SNI_249_2025. eCollection 2025.

Abstract

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.

摘要

背景

多发性骨髓瘤(MM)通常累及骨髓。当它扩散至中枢神经系统时,通常表现为颅内转移或硬膜外脊髓病变。硬膜内脊髓转移极为罕见。

病例描述

一名53岁男性,患有免疫球蛋白Aκ型MM,在T3 - 4水平出现一个强化病灶,由一个硬膜内病灶和一个通过椎间孔延伸的硬膜外病灶组成。病灶特征提示为神经鞘瘤,但鉴于患者病史怀疑有MM累及。进行了手术切除和脊柱固定,病理检查证实为浆细胞瘤。对文献的系统回顾发现了10例与MM或孤立性浆细胞瘤相关的硬膜内脊髓病变病例。大多数病变为硬膜内髓外,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,尤其是伴有软脑膜播散时。

结论

本病例突出了硬膜内脊髓MM累及的诊断和治疗挑战。虽然手术可以缓解症状并确诊,但软脑膜播散的风险需要密切监测。多学科方法对于管理这些罕见且复杂的病例至关重要,需要进一步研究以完善治疗策略并改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db35/12255213/130c9d711cae/SNI-16-247-g001.jpg

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