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手掌和手腕正中神经脂肪过多症次全切除术后进行性神经区域过度生长:1 例病例报告、文献复习及范例。

Progressive nerve territory overgrowth after subtotal resection of lipomatosis of the median nerve in the palm and wrist: a case, a review and a paradigm.

机构信息

Department of Neurologic Surgery, Mayo Clinic, Gonda 8-214, Rochester, MN 55905, USA.

出版信息

Acta Neurochir (Wien). 2013 Jun;155(6):1131-41. doi: 10.1007/s00701-013-1707-z. Epub 2013 Apr 25.

Abstract

BACKGROUND

Lipomatosis of the nerve (LN) is a rare disorder characterized by the massive enlargement of peripheral nerves, frequently accompanied by generalized fibroadipose proliferation and skeletal overgrowth. The treatment of this disorder remains controversial, in part because of the rarity and the variability of presentation. Some authors have advocated total resection of this benign lesion including the functioning nerve, while others recommend symptomatic decompression alone.

METHODS

We have been routinely following a 10-year-old boy for lipomatosis of the median nerve at the wrist noted shortly after birth. He underwent median nerve resection accompanied by sural nerve grafting at another institute. We review the literature on LN and the efficacy of nerve grafting.

RESULTS

Clinically, he made a good recovery, with mild loss of thenar function and relatively preserved sensation. Serial magnetic resonance imaging over 5 years has revealed progression of the LN at both coaptation sites, fibrofatty proliferation within the nerve grafts as well as distal digital nerves, and enlargement of a fibrous scar at the coaptation sites. This has never been reported in the 9 decades of study of this disease.

CONCLUSION

We present the first medium-term follow-up of a patient who underwent nerve sacrifice to attempt to cure the LN alongside a historical review of treatment. We believe that macroscopic gross total resection (i.e., microscopic subtotal resection) is insufficient in stopping the potential progression of this hamartomatous lesion because of the persistent effect of trophic factors.

摘要

背景

神经脂肪瘤病(LN)是一种罕见的疾病,其特征是周围神经的大量肿大,常伴有广泛的纤维脂肪增生和骨骼过度生长。这种疾病的治疗仍然存在争议,部分原因是其罕见性和表现的多样性。一些作者主张对这种良性病变进行包括功能神经在内的全切除,而另一些作者则建议仅进行症状性减压。

方法

我们一直在常规随访一位 10 岁男孩,他在出生后不久就被诊断为腕部正中神经脂肪瘤病。他曾在另一家机构接受正中神经切除术和腓肠神经移植。我们回顾了关于 LN 和神经移植疗效的文献。

结果

临床方面,他恢复良好,大鱼际肌功能轻度丧失,感觉相对保留。5 年来的连续磁共振成像显示 LN 在吻合部位进展,神经移植内和远端指神经纤维脂肪增生,以及吻合部位纤维疤痕增大。这在该疾病 90 年的研究中从未报道过。

结论

我们报告了首例接受神经牺牲以试图治愈 LN 的患者的中期随访,并对治疗进行了历史回顾。我们认为,由于营养因子的持续作用,宏观大体全切除(即微观次全切除)不足以阻止这种错构瘤样病变的潜在进展。

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