Microsurgical resection of an intramedullary metastasis of rare histopathology-a case report and comprehensive literature review.

Q1 Medicine
Journal of spine surgery Pub Date : 2025-06-27 Epub Date: 2025-05-12 DOI:10.21037/jss-24-115
Felix C Stengel, Stephan Heisinger, Natalia Vélez Char, Anand Veeravagu, Martin N Stienen
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Abstract

Background: Intramedullary spinal cord metastases (ISCMs) are rare manifestations of systemic malignancy, accounting for 4-9% of central nervous system metastases. Radio- and chemotherapy are considered first-line therapies. However, certain clinical presentations may require microsurgical resection of ISCM. The optimal treatment strategy remains controversial, particularly in cases with diagnostic uncertainty or rapid neurological deterioration.

Case description: We present a 59-year-old female patient with history of treated breast cancer who developed progressive, burning pain in the left groin radiating to the ventral thigh and knee, accompanied by sensory deficits and gait instability. Magnetic resonance imaging (MRI) revealed a contrast-enhancing intramedullary lesion at T10 with extensive perifocal edema from C7 to L1. Given the unclear etiology and worsening neurological symptoms, microsurgical resection was performed using intraoperative neuromonitoring and ultrasound guidance. Histopathological examination unexpectedly revealed a metastasis from a previously undiagnosed amelanotic melanoma, rather than the suspected breast cancer metastasis. Subsequent screening identified an additional right inguinal lymph node metastasis, which was surgically removed. The patient received adjuvant radiation therapy to T9-11 (13×2.5 Gy) and immunotherapy with nivolumab. At 3 years post-operation, the patient maintains good functional status with no evidence of tumor recurrence.

Conclusions: This case highlights the value of microsurgical resection in providing both therapeutic benefit and definitive diagnosis and the importance of comprehensive histopathological evaluation even when a likely primary tumor exists. Larger, multicenter data collections are required to better delineate the role of microsurgery in ISCM treatment and to establish evidence-based guidelines for patient selection.

显微手术切除髓内转移罕见病理组织1例并文献复习。
背景:髓内脊髓转移是一种罕见的全身性恶性肿瘤,占中枢神经系统转移的4-9%。放疗和化疗被认为是一线治疗。然而,某些临床表现可能需要显微手术切除ISCM。最佳治疗策略仍然存在争议,特别是在诊断不确定或神经系统迅速恶化的情况下。病例描述:我们报告了一名59岁的女性患者,她有乳腺癌治疗史,她出现了进行性,左侧腹股沟放射到大腿腹侧和膝盖的灼烧性疼痛,并伴有感觉缺陷和步态不稳定。磁共振成像(MRI)显示T10处增强的髓内病变伴从C7到L1广泛的局灶周围水肿。鉴于病因不明,神经系统症状加重,术中神经监测及超声引导下行显微外科手术切除。组织病理学检查出乎意料地发现一个以前未诊断的无色素黑色素瘤的转移,而不是怀疑乳腺癌转移。随后的筛查发现了一个额外的右腹股沟淋巴结转移,手术切除。患者接受T9-11辅助放射治疗(13×2.5 Gy)和纳武单抗免疫治疗。术后3年,患者功能状态良好,无肿瘤复发迹象。结论:本病例强调了显微外科切除在提供治疗效益和明确诊断方面的价值,以及即使存在可能的原发肿瘤时也要进行全面的组织病理学评估的重要性。需要更大的、多中心的数据收集来更好地描述显微外科在ISCM治疗中的作用,并为患者选择建立循证指南。
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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来源期刊
Journal of spine surgery
Journal of spine surgery Medicine-Surgery
CiteScore
5.60
自引率
0.00%
发文量
24
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