一种罕见的手部和腕部伏面分裂瘤病:病例报告

Muge Kirac , Abdullah Burak Kara , Halil Ibrahim Bulut , Gulcin Basdemir , Danyal Gumus , Korhan Ozkan
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引用次数: 0

摘要

背景斯旺瘤又称神经瘤,是最常见的周围神经肿瘤。这些肿瘤生长缓慢,在确诊前数年会出现无痛性肿胀。本报告旨在介绍一例非常罕见的起源于第二根数字神经的丛状分裂瘤,以及起源于第三、第四根数字神经和正中神经掌皮支的多发性分裂瘤,重点介绍鉴别诊断和治疗策略。手术切除两次,保留了神经和肌腱。之后复发,活检证实为良性神经鞘瘤。显微镜检查发现,较大的病变为多结节/丛状分裂瘤,其他病变为单纯分裂瘤,因此诊断为多发性分裂瘤病。结论手术治疗可以治愈并有效地治疗并发的裂孔瘤肿瘤。尽管如此,经过精心策划和实施,手术治疗仍是并发分裂瘤患者的一个很有前途的选择。要充分了解手术治疗的效果并完善其技术,还需要进一步的研究和长期随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare form of schwannomatosis on the volar surface of the hand and wrist: A case report

Background

Schwannomas, which are also known as neurilemomas, constitute the most common type of peripheral nerve tumors. These tumors can grow slowly and occur as painless swellings over the course of several years before their diagnosis. The aim of this report is to present a case of a very rare plexiform schwannoma originating from second digital nerve and multiple schwannomas from third and fourth digital nerves and palmar cutaneous branch of median nerve with emphasis given on differential diagnosis and treatment strategy.

Case Presentation

A 15-year-old patient presented with soft tissue masses on the volar surface of the hand, initially diagnosed as benign nerve sheath tumors. Surgical excision was performed twice, preserving nerves and tendons. Recurrence occurred, and subsequent biopsy confirmed benign nerve sheath tumors. Microscopic examination revealed multinodular/plexiform schwannoma in the larger lesion and simple schwannomas in others, leading to a diagnosis of multiple schwannomatosis. All surgeries resulted in intact sensory and motor function.

Conclusion

Surgical treatment can be curative and effectively employed for concomitant schwannoma tumors. Nevertheless, with careful planning and execution, surgery remains a promising option for patients with concomitant schwannomas. Further research and long-term follow-up studies are needed to fully understand the outcomes and refine the techniques used in these surgical treatments.

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