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正中神经脂肪纤维黏液瘤切除及神经移植:病例报告。

Resection and nerve grafting of a lipofibrohamartoma of the median nerve: case report.

机构信息

Department of Neurosurgery, Louisiana State University Health Science Center, New Orleans, Louisiana 70112, USA.

出版信息

Neurosurgery. 2009 Oct;65(4 Suppl):A229-35. doi: 10.1227/01.NEU.0000345353.21320.1F.

Abstract

OBJECTIVE AND IMPORTANCE

Our patient's symptomatology, history, physical examination, diagnosis, management, and functional outcome 1 year after surgical repair is presented and discussed in light of the current literature on lipofibrohamartomas.

CLINICAL PRESENTATION

A 3-year-old boy presented to the Louisiana State University Nerve Clinic for evaluation and management because he was experiencing progressive symptoms of left hand swelling, dysesthesia, and impaired motor function. Physical examination demonstrated median nerve distribution motor impairment. Electromyographic/nerve conduction velocity studies also showed severely reduced conduction and amplitude of the median nerve response, and the magnetic resonance imaging findings were highly suggestive of lipofibrohamartoma. Hence, the presumed diagnosis was lipofibrohamartoma on the basis of imaging characteristics, location, and patient's age.

INTERVENTION

The patient was brought to the operating room with the objectives of carpal tunnel release and biopsy. However, routine intraoperative nerve action potential recordings showed no or very poor responses, consistent with significant loss of median nerve function. On the basis of the intraoperative nerve action potentials, we opted to resect the tumor back to healthy median nerve fascicles and to perform graft repairs. Surgery proceeded uneventfully, without any complications. Pathology confirmed the diagnosis of lipofibrohamartoma.

CONCLUSION

At 18 months postoperatively, the patient had excellent left hand function. On the basis of our experience with this patient, we believe that intraoperative nerve action potentials and the availability of usable proximal and distal nerve fascicles (which may be discernible on diagnostic imaging) are key factors in deciding whether a lipofibrohamartoma needs to be repaired or decompressed/biopsied. As illustrated by our case, we believe that resection and graft repair may be the best treatment option for some of these patients, and perhaps more so for pediatric patients.

摘要

目的和重要性

我们呈现并讨论了一位患者的症状、病史、体格检查、诊断、治疗和手术修复 1 年后的功能结果,同时结合了关于脂肪纤维黏液样错构瘤的当前文献。

临床表现

一名 3 岁男孩因左手肿胀、感觉异常和运动功能受损的症状逐渐加重,到路易斯安那州立大学神经诊所就诊进行评估和治疗。体格检查显示正中神经分布运动功能障碍。肌电图/神经传导速度研究也显示正中神经反应的传导和幅度严重降低,磁共振成像结果高度提示脂肪纤维黏液样错构瘤。因此,根据影像学特征、位置和患者年龄,推测诊断为脂肪纤维黏液样错构瘤。

干预措施

患者被带到手术室进行腕管松解和活检。然而,常规术中神经动作电位记录显示无反应或反应非常差,与正中神经功能严重丧失一致。根据术中神经动作电位,我们选择切除肿瘤至健康的正中神经束,并进行移植物修复。手术顺利进行,无任何并发症。病理证实了脂肪纤维黏液样错构瘤的诊断。

结论

术后 18 个月,患者左手功能良好。根据我们对该患者的经验,我们认为术中神经动作电位和可用的近端和远端神经束(在诊断成像上可能可见)是决定脂肪纤维黏液样错构瘤是否需要修复或减压/活检的关键因素。正如我们的病例所示,我们认为切除和移植物修复可能是一些患者的最佳治疗选择,对于儿科患者更是如此。

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