指神经丛状神经鞘瘤。

IF 0.5 Q4 SURGERY Journal of Hand Surgery-Asian-Pacific Volume Pub Date : 2023-10-01 Epub Date: 2023-10-25 DOI:10.1142/S2424835523720190
Yuji Saeki, Yasunori Hattori, Satish Annabhau Mane, Kazuteru Doi
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引用次数: 0

摘要

丛状神经鞘瘤是一种罕见的良性肿瘤,以丛状生长。我们报告了一名47岁的男子,他患有右手食指掌指关节掌侧的肿块,该肿块已经逐渐生长了10多年。从腕管远端到食指近端指间关节尺侧触诊肿块,有刺痛感和麻木感。该肿瘤是一个多结节性肿瘤,涉及指掌总神经至尺侧指掌固有神经。它被切除并用腓肠神经移植物重建。丛状神经鞘瘤在指神经中很少见,只有6例报告。一般来说,经典神经鞘瘤可以在不引起神经功能缺损的情况下摘除;然而,丛状神经鞘瘤可能需要神经切除术。有关于丛状神经鞘瘤复发的报道;最终切除和长期随访是必要的。证据等级:五级(治疗)。
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Plexiform Schwannoma of Digital Nerve.

Plexiform schwannoma is an uncommon benign tumour that grows in a plexiform pattern. We report a 47-year-old man with a mass on the palmar aspect of the metacarpophalangeal joint of the right index finger that had been growing gradually for more than 10 years. The mass was palpated from the distal carpal tunnel to the ulnar aspect of the proximal interphalangeal joint of the index finger, with tingling and numbness sensation. The tumour was a multinodular tumour involving the first common palmar digital nerve to the ulnar proper palmar digital nerve. It was resected and reconstructed with a sural nerve graft. Plexiform schwannoma is rare in the digital nerve, with only six cases reported. Generally, classic schwannomas can be enucleated without causing neurologic deficits; however, plexiform schwannoma may require nerve resection. There have been reports of recurrence of plexiform schwannoma; definitive resection and long-term follow-up are necessary. Level of Evidence: Level V (Therapeutic).

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