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A giant plexiform schwannoma of the brachial plexus: case report

机译:臂丛神经丛状神经鞘瘤

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摘要

We report the case of a patient who noticed muscle weakness in his left arm 5 years earlier. On examination, a biloculate mass was observed in the left supraclavicular area, and Tinel's sign caused paresthesia in his left arm. Magnetic resonance imaging showed a continuous, multinodular, plexiform tumor from the left C5 to C7 nerve root along the course of the brachial plexus to the left brachia. Tumor excision was attempted. The median and musculocutaneous nerves were extremely enlarged by the tumor, which was approximately 40 cm in length, and showed no response to electric stimulation. We resected a part of the musculocutaneous nerve for biopsy and performed latissimus dorsi muscle transposition in order to repair elbow flexion. Morphologically, the tumor consisted of typical Antoni A areas, and immunohistochemistry revealed a Schwann cell origin of the tumor cells moreover, there was no sign of axon differentiation in the tumor. Therefore, the final diagnosis of plexiform Schwannoma was confirmed.
机译:我们报告了一名患者,该患者5年前注意到左臂肌肉无力。检查时,在左锁骨上区域观察到双灶性肿块,Tinel的体征引起左臂感觉异常。磁共振成像显示,从左C5到C7神经根沿着臂丛神经一直到左臂,出现连续的多结节状丛状肿瘤。尝试切除肿瘤。正中和肌肉皮肤神经被肿瘤极大地扩大,其长度约为40cm,并且对电刺激没有反应。我们切除了一部分肌皮神经以进行活检,并进行了背阔肌移位术以修复肘关节屈曲。形态上,肿瘤由典型的Antoni A区组成,免疫组织化学还显示肿瘤细胞是雪旺氏细胞起源,在肿瘤中没有轴突分化的迹象。因此,证实了对丛状神经鞘瘤的最终诊断。

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