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局限性肥厚性神经病的切除与移植修复术

Resection and graft repair for localized hypertrophic neuropathy.

作者信息

Gruen J P, Mitchell W, Kline D G

机构信息

Department of Neurological Surgery, School of Medicine, University of Southern California, Los Angeles 90033, USA.

出版信息

Neurosurgery. 1998 Jul;43(1):78-83. doi: 10.1097/00006123-199807000-00051.

Abstract

OBJECTIVES

Formulation of surgical management recommendations for localized hypertrophic mononeuropathy has been difficult because of the infrequency of the lesion, lack of precise pathological diagnosis, and uncertainties regarding its cause. The purpose of this retrospective review of the Louisiana State University (LSU) experience with this unusual neuropathy was to evaluate the efficacy of lesion resection and interposition grafting in its management.

METHODS

The charts of 15 patients operated on at LSU during a 15-year period with a pathological diagnosis of localized hypertrophic neuropathy were reviewed.

RESULTS

Hypertrophic lesions were located on major named peripheral nerves of the extremities, distributed equally to the upper and lower extremities. Family history was negative for all patients, and entrapment or trauma, other than previous surgery, were unlikely by symptom location or history. Weakness was the most common presentation. The mean length of symptoms was 76 months. Atrophy, sensory loss, Tinel's sign, focal tenderness, and a mass were found in the majority of patients. Preoperative electrophysiological studies showed chronic denervational changes in all patients. At surgery, if no action potential or one of low amplitude was recorded across the lesion, the lesion was resected and an autologous nerve graft measuring from 3.5 to 8.5 cm in length was interposed. During follow-up periods of 1 or more years, seven of nine patients with localized hypertrophic mononeuropathy treated with graft repairs were either unchanged or improved.

CONCLUSION

Localized hypertrophic mononeuropathy is a progressive process associated with pathological nerve changes that correlate with eventual severe functional loss. If intraoperative histological examination shows onion bulb neuropathy and intraoperative nerve action potentials confirm a nonfunctioning or poorly functioning segment, lesion resection with interposition graft repair provides the possibility of some degree of recovery.

摘要

目的

由于局部肥厚性单神经病损罕见、缺乏精确的病理诊断以及病因不明,制定其外科治疗建议一直很困难。对路易斯安那州立大学(LSU)处理这种罕见神经病的经验进行回顾性研究的目的,是评估病损切除及移植修复在其治疗中的疗效。

方法

回顾了LSU在15年期间对15例经病理诊断为局部肥厚性神经病患者的手术记录。

结果

肥厚性病变位于四肢主要的命名周围神经,上下肢分布均等。所有患者家族史均为阴性,根据症状部位或病史判断,除既往手术外,不太可能存在卡压或创伤。无力是最常见的表现。症状的平均持续时间为76个月。大多数患者存在萎缩、感觉丧失、Tinel征、局部压痛及肿块。术前电生理研究显示所有患者均有慢性失神经改变。手术时,如果在病损处未记录到动作电位或记录到低幅动作电位,则切除病损并植入一段长度为3.5至8.5厘米的自体神经移植物。在1年或更长时间的随访期内,接受移植修复治疗的9例局部肥厚性单神经病患者中有7例病情无变化或有所改善。

结论

局部肥厚性单神经病是一个与病理性神经改变相关的进行性过程,这些改变与最终严重的功能丧失相关。如果术中组织学检查显示有洋葱球样神经病,且术中神经动作电位证实有一段神经无功能或功能不良,则切除病损并进行移植修复有可能使病情得到一定程度的恢复。

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