胸腔髓内中分级黑色素细胞瘤不理想的神经系统预后--系统综述与案例说明

Cancers Pub Date : 2024-05-14 DOI:10.3390/cancers16101867
Marco Battistelli, Fulvio Grilli, A. Rapisarda, Michele Di Domenico, Nicola Montano, Marco Gessi, Alessandro Olivi, Alessio Albanese, F. Polli
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引用次数: 0

摘要

背景:髓内黑色素细胞瘤极为罕见,迄今为止仅有 24 例报道。尽管它们具有良性生物学行为,但表现为局部浸润性肿瘤。试图完全安全切除往往会导致术后严重的神经功能缺损,就像我们这里的病例一样。研究方法对 PubMed 和 Scopus 数据库中截至 2024 年 2 月发表的研究进行了系统回顾。结果:共纳入 19 项研究:共纳入 19 项研究,涵盖 24 个病例。性别分布相似(男:女 13:11),年龄从 19 岁到 79 岁不等。胸段患者最多,中度黑色素细胞瘤(19 例)是最常见的组织类型。从影像学角度看,髓内黑色素细胞瘤通常表现为中央管外围的高密度出血性病变,并伴有局灶性结节强化。术中,它们呈黑红色至棕褐色,是顽固的粘连性病变。在抽样研究中,IONM的就业情况并不常见,有16例描述了术后新出现的神经功能缺损。有四例病例使用了辅助 RT,其价值值得商榷。复发很常见(10 例),辅助疗法(RT 或重复手术)似乎起到了缓解作用。病例介绍:一名 68 岁的妇女因痉挛性截瘫恶化和丧失日常生活自理能力(麦考密克 4 级)就诊 3 年。核磁共振成像检查发现了一个从Th5到Th7的髓内肿瘤,其特征是T1加权高密度和近期髓内出血的迹象。在多模态神经监测(包括D波)的指导下,切除了一个黑褐色的肿瘤,该肿瘤血管扩张,与白质紧密粘连。在对病灶进行最后解剖以获得全切除术(GTR)时,记录到 MEPs 和 D 波信号急剧下降。术后,患者出现了严重的低麻痹,Th9水平和节段性运动障碍,在神经康复治疗期间有所改善。组织病理学检查显示为中度黑色素细胞瘤(中枢神经系统 WHO 2021 分类)。四个月的随访表明该患者没有复发。结论:这篇文献综述强调,成年患者胸部髓内T1高张力出血性病变应引起对髓内黑色素细胞瘤的怀疑。这些肿瘤具有局部侵袭性,通常会导致术后神经功能缺损,而且经常复发,使治疗策略不堪重负,数年后只能接受姑息治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unsatisfactory Neurological Outcome in an Intramedullary Thoracic Intermediate-Grade Melanocytoma—Systematic Review and Illustrative Case
Background: Intramedullary melanocytomas are exceedingly rare, with only twenty-four cases reported up to now. They present as local invasive tumors despite their benign biological behavior. Attempting a complete safe resection often results in severe post-operative neurological deficits, as in our case presented here. Methods: A systematic review was conducted across the PubMed and Scopus databases including studies published till February 2024. Results: A total of 19 studies were included, encompassing 24 cases. A similar distribution between sexes was noted (M:F 13:11), with ages ranging from 19 to 79 years. The thoracic segment was most affected, and intermediate-grade melanocytoma (19 cases) was the most common histotype. Radiographically, intramedullary melanocytomas usually appear as hyperintense hemorrhagic lesions peripheral to the central canal with focal nodular enhancement. Intraoperatively, they are black–reddish to tan and are tenaciously adherent lesions. In the sampled studies, IONM employment was uncommon, and post-operative new-onset neurological deficits were described in 16 cases. Adjuvant RT was used in four cases and its value is debatable. Recurrence is common (10 cases), and adjuvant therapies (RT or repeated surgery) seem to play a palliative role. Case presentation: A 68-year-old woman presented with a three-year history of worsening spastic paraparesis and loss of independence in daily activities (McCormick grade 4). An MRI revealed an intramedullary tumor from Th5 to Th7, characterized by T1-weighted hyperintensity and signs of recent intralesional hemorrhage. Multimodal neuromonitoring, comprising the D-Wave, guided the resection of a black–tan-colored tumor with hyper-vascularization and strong adherence to the white matter. During final dissection of the lesion to obtain gross total resection (GTR), a steep decline in MEPs and D-Wave signals was recorded. Post-operatively, the patient had severe hypoesthesia with Th9 level and segmental motor deficits, with some improvement during neurorehabilitation. Histopathology revealed an intermediate-grade melanocytoma (CNS WHO 2021 classification). A four-month follow-up documented the absence of relapse. Conclusions: This literature review highlights that intramedullary T1 hyperintense hemorrhagic thoracic lesions in an adult patient should raise the suspicion of intramedullary melanocytoma. They present as locally aggressive tumors, due to local invasiveness, which often lead to post-operative neurological deficits, and frequent relapses, which overwhelm therapeutic strategies leading to palliative care after several years.
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