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Sarcomatoid Malignant Mesothelioma Presenting with Intramedullary Spinal Cord Metastasis: A Case Report and Literature Review

机译:肉瘤样恶性间皮瘤伴髓内脊髓转移:一例报道并文献复习

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摘要

>Study Design Case report. >Objective Malignant mesothelioma (MM) is an uncommon tumor of the pleural epithelium with a predilection for local spread into adjacent tissues. The sarcomatoid type accounts for ∼10% of MM cases and is associated with poorer survival than the epithelioid, desmoplastic, and biphasic types. MM commonly presents with involvement of the vertebral body or epidural space. However, intradural spinal extension of MM is extremely rare. Only eight cases of intradural spinal extension have been reported. We report this rare case and discuss the clinical manifestations of intradural spinal extension of MM with literature review. >Methods This report describes the case of a 62-year-old man with Brown-Séquard syndrome and radiculopathy of the left C5 nerve root detected during treatment for pleural sarcomatoid MM. Magnetic resonance imaging (MRI) showed an intramedullary lesion at the C3 level and a small nodule at the left C5 nerve root with cervical canal stenosis. >Results The patient underwent surgery, and intramedullary metastasis of sarcomatoid MM was diagnosed. Subsequently, radiotherapy was administered, resulting in temporary improvement of the patient's condition. Thereafter, his condition gradually deteriorated, and follow-up MRI showed a more extensive residual C3 intramedullary lesion. Thus, a second surgery was performed after chemotherapy, but the patient died 5 months after the initial diagnosis. >Conclusion We present this rare case, and emphasize intramedullary spinal cord metastasis of MM as differential diagnosis in primary cord lesion.
机译:>研究设计案例报告。 >客观恶性间皮瘤(MM)是一种罕见的胸膜上皮肿瘤,易局部扩散到邻近组织。肉瘤类型约占MM病例的10%,与上皮样,增生和双相型相比,其生存期较差。 MM通常表现为累及椎体或硬膜外腔。但是,MM的硬脊膜内延伸极为罕见。仅报告了八例硬膜内脊柱延伸。我们报告这种罕见的情况,并通过文献复习讨论硬膜内硬膜外MM的临床表现。 >方法该报告介绍了一位62岁的男子,该病人患有Brown-Séquard综合征,在治疗胸膜肉瘤MM时发现左C5神经根神经根神经根病。磁共振成像(MRI)显示C3水平的髓内病变和左C5神经根的小结节,并伴有宫颈管狭窄。 >结果该患者接受了手术,并被诊断为肉瘤样MM的髓内转移。随后,进行放射治疗,导致患者病情暂时改善。此后,他的病情逐渐恶化,随后的MRI显示更广泛的残留C3髓内病变。因此,化疗后进行了第二次手术,但是患者在最初诊断后的5个月内死亡。 >结论我们介绍了这种罕见病例,并强调了MM的髓内脊髓转移作为原发性病变的鉴别诊断。

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