Fibrolipomatous Hamartoma of the Median Nerve: An Outcome of Surgical Management in Six Consecutive Cases.

Nigerian Journal of Surgery Pub Date : 2020-07-01 Epub Date: 2020-07-27 DOI:10.4103/njs.NJS_16_20
Avinash Prabhu, R Anil, Niranjan Kumar
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引用次数: 4

Abstract

Background: Lipoma is a nonneurogenic benign tumor. Neurolipoma and fibrolipomatous hamartoma are variants of this universal tumor. All these variants are grouped under lipomatosis of the nerve. Majority of these tumors are asymptomatic, which can be observed. Symptomatic patients require surgery, which is not standardized. As there are insufficient number of cases, no randomized controlled studies have been performed in the treatment of fibrolipomatous hamartoma. The aim of our study was to determine the pattern of presentation of fibrolipomatous hamartoma, surgical management offered, and the outcome in the form of recovery and complications.

Materials and methods: This retrospective descriptive study includes six patients diagnosed with fibrolipomatous hamartoma over a period of 12 years. Patient details were collected from the medical records. Patients diagnosed of fibrolipomatous hamartoma in the hand were included. Patients with other soft-tissue tumors were excluded from the study. Out of six patients, four required excision of nerve followed by reconstruction using sural nerve graft and two underwent microsurgical dissection of neural element. Patients were instructed to take care of the operated hand during the recovery phase. Institutional physiotherapy protocol was started during the 3rd postoperative week. Follow-up period was between 1 and 3 years.

Results: All the six patients were free from symptoms postoperatively. Minimal complications were noted in two patients, which were managed conservatively.

Conclusion: Surgical excision of fibrolipomatous hamartoma of median nerve below elbow, with nerve dissection or with nerve reconstruction using sural nerve graft, followed by proper postoperative care and physiotherapy has proven beneficial for the patients in our study.

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正中神经纤维脂肪瘤错构瘤:连续6例手术治疗的结果。
背景:脂肪瘤是一种非神经源性良性肿瘤。神经脂肪瘤和纤维脂肪瘤错构瘤是这种普遍肿瘤的变体。所有这些变异都归为神经脂肪瘤病。这些肿瘤大多数是无症状的,这是可以观察到的。有症状的患者需要手术,但手术并不规范。由于病例数量不足,尚无纤维脂肪瘤错构瘤治疗的随机对照研究。我们研究的目的是确定纤维脂肪瘤错构瘤的表现模式,手术治疗方案,以及恢复和并发症的结果。材料和方法:本回顾性描述性研究包括6例诊断为纤维脂肪瘤错构瘤的患者,时间超过12年。从医疗记录中收集了患者的详细信息。诊断为手部纤维脂肪瘤错构瘤的患者也包括在内。其他软组织肿瘤患者被排除在研究之外。在6例患者中,4例需要切除神经,然后用腓肠神经移植重建,2例接受显微外科解剖神经元件。患者被指示在恢复阶段照顾手术的手。术后第3周开始机构物理治疗方案。随访期1 - 3年。结果:6例患者术后均无症状。2例患者并发症极少,均予保守治疗。结论:手术切除肘关节下正中神经纤维脂肪瘤错构瘤,行神经剥离或腓肠神经移植重建,术后适当的护理和物理治疗对患者是有益的。
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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