Rossi Marco, Viganò Luca, Puglisi Gugliemo, Conti Nibali Marco, Leonetti Antonella, Gay Lorenzo, Sciortino Tommaso, Fornia Luca, Callipo Vincenzo, Lamperti Marta, Riva Marco, Cerri Gabriella, Bello Lorenzo
Neurosurgical Oncology Unit, Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milano, Italy.
Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, 20147 Milano, Italy.
Cancers (Basel). 2021 Jul 28;13(15):3808. doi: 10.3390/cancers13153808.
Primary-Motor-Cortex (M1) hosts two functional components, at its posterior and anterior borders, being the first faster and more excitable. We developed a mapping-technique for M1 components identification and determined their functional cortical-subcortical architecture in M1 gliomas and the impact of their identification on tumor resection and motor performance. A novel advanced mapping technique was used in 102 tumors within M1 or CorticoSpinal-Tract to identify M1-two components. High-Frequency-stimulation (2-5 pulses) with an on-line qualitative and quantitative analysis of motor responses was used; the two components' cortical/subcortical spatial distribution correlated to clinical, tumor-related factor and patients' motor outcome; a cohort treated with standard-mapping was used for comparison. The two functional components were always identified on-line; in tumors not affecting M1, its functional segregation was preserved. In M1 tumors, two architectures, both preserving the two components, were disclosed: in 50%, a normal cortical/subcortical architecture emerged, while 50% revealed a distorted architecture with loss of anatomical reference and somatotopy, not associated with tumor histo-molecular features or volume, but with a previous treatment. Motor performance was maintained, suggesting functional compensation. By preserving the highest and resecting the lowest excitability component, the complete-resection increased with low morbidity. The real-time identification of two M1 functional components and the preservation of the highest excitability one increases safe resection, revealing M1 plasticity potentials.
初级运动皮层(M1)在其后部和前部边界有两个功能成分,其中第一个更快且更易兴奋。我们开发了一种用于识别M1成分的映射技术,并确定了它们在M1胶质瘤中的功能性皮质-皮质下结构,以及它们的识别对肿瘤切除和运动功能的影响。一种新型的先进映射技术用于M1或皮质脊髓束内的102个肿瘤,以识别M1的两个成分。使用高频刺激(2-5个脉冲)并对运动反应进行在线定性和定量分析;两个成分的皮质/皮质下空间分布与临床、肿瘤相关因素及患者的运动结果相关;使用一组接受标准映射的患者作为对照。两个功能成分总能在线识别;在未影响M1的肿瘤中,其功能分离得以保留。在M1肿瘤中,发现了两种均保留两个成分的结构:50%呈现正常的皮质/皮质下结构,而50%显示结构扭曲,解剖学参照和躯体定位丧失,这与肿瘤的组织分子特征或体积无关,而是与先前的治疗有关。运动功能得以维持,提示存在功能代偿。通过保留兴奋性最高的成分并切除兴奋性最低的成分,全切率提高且发病率降低。实时识别M1的两个功能成分并保留兴奋性最高的成分可提高手术切除的安全性,揭示M1的可塑性潜能。