Upper Extremity Surgery in Hirayama Disease: A Modification of the Current Algorithm.

IF 1.6 4区 医学 Q3 SURGERY
Annals of Plastic Surgery Pub Date : 2025-05-01 Epub Date: 2025-02-13 DOI:10.1097/SAP.0000000000004299
Elad Y Holzer, Tod A Clark, Jennifer L Giuffre
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引用次数: 0

Abstract

Introduction: Hirayama disease (HD) is a rare, nonfamilial, monomelic amyotrophy in which patients present with muscle atrophy and weakness of the forearms and hands, either unilateral or bilateral, and without sensory loss. Current treatment guidelines describe the role of conservative treatments including cervical collars and neurotropic medications, as well as spinal surgery in select patients. Upper extremity surgery has not yet been incorporated into the treatment algorithm of HD. The objective of this study is twofold: to present a case series of HD patients treated with the incorporation of nerve and tendon transfers and joint fusions into the existing treatment algorithm and to perform a literature review of interventions.

Methods: Three cases (4 limbs) of HD treated surgically with nerve and tendon transfers and fusion are retrospectively reviewed. The subjective and objective results from surgery are reported. A literature review is performed on PubMed using "Hirayama disease" and "peripheral nerve surgery," "nerve transfer," "tendon transfer," "hand surgery," or "upper extremity surgery" as search terms to identify studies describing surgical treatment of HD outside of spinal surgery.

Results: Three HD patients (4 limbs) were identified. The average age was 23 years old (range, 16-33 years). Patients presented with intrinsic muscle atrophy, hypothenar, and thenar atrophy. The disease had been present for an average of 6.5 years (range, 1.5-15 years) prior to referral. Two patients had unilateral involvement, whereas one had bilateral involvement. Two patients (3 limbs) were treated with an anterior interosseous (AIN) to ulnar motor nerve transfer, whereas a patient with delayed presentation underwent thumb metacarpophalangeal joint fusion and a Zancolli lasso to the fingers. All patients had subjective and objective improvements postoperation.The literature reveals three independent case reports of HD patients treated with upper extremity surgery. Two papers describe using a tendon transfer, whereas one paper describes an AIN to ulnar motor nerve transfer. All patients demonstrated functional improvements in follow-up.

Conclusions: HD can be successfully treated with a combination of upper extremity surgery and nerve transfers. To the authors' knowledge, this is the first literature review and the largest case series presenting such interventions in HD.

平山病的上肢手术:当前算法的改进。
平山病(Hirayama disease, HD)是一种罕见的非家族性单侧肌萎缩症,患者表现为单侧或双侧前臂和手部肌肉萎缩和无力,无感觉丧失。目前的治疗指南描述了保守治疗的作用,包括颈套和神经药物,以及在选定的患者中进行脊柱手术。上肢手术尚未被纳入HD的治疗方案。本研究的目的有两个:一是介绍将神经和肌腱转移及关节融合纳入现有治疗算法的HD患者病例系列,二是对干预措施进行文献综述。方法:回顾性分析手术治疗HD 3例(4肢)的神经、肌腱转移融合。报告了手术的主观和客观结果。在PubMed上使用“平山病”和“周围神经手术”、“神经转移”、“肌腱转移”、“手部手术”或“上肢手术”作为搜索词进行文献综述,以确定描述脊柱手术外HD手术治疗的研究。结果:确诊HD患者3例(4肢)。平均年龄23岁(范围16-33岁)。患者表现为内在肌萎缩、鱼际下、鱼际萎缩。该疾病在转诊前平均存在6.5年(范围,1.5-15年)。两名患者单侧受累,一名患者双侧受累。2例患者(3条肢体)采用前骨间(AIN)到尺侧运动神经转移治疗,而1例延迟出现的患者接受拇指掌指关节融合术和手指Zancolli套索。所有患者术后主客观均有改善。文献揭示了三个独立的病例报告,HD患者治疗上肢手术。两篇论文描述了使用肌腱转移,而一篇论文描述了AIN到尺侧运动神经转移。所有患者在随访中均表现出功能改善。结论:采用上肢手术和神经转移相结合的方法可以成功治疗HD。据作者所知,这是首次文献综述和最大的病例系列,介绍了HD的此类干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
13.30%
发文量
584
审稿时长
6 months
期刊介绍: The only independent journal devoted to general plastic and reconstructive surgery, Annals of Plastic Surgery serves as a forum for current scientific and clinical advances in the field and a sounding board for ideas and perspectives on its future. The journal publishes peer-reviewed original articles, brief communications, case reports, and notes in all areas of interest to the practicing plastic surgeon. There are also historical and current reviews, descriptions of surgical technique, and lively editorials and letters to the editor.
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