Prabhu Avinash, Anil R, Kumar Niranjan
Department of Plastic Surgery, SDM College of Medical Sciences and Hospital, Dharwad, Karnataka, India.
Niger J Surg. 2020 Jul-Dec;26(2):153-158. doi: 10.4103/njs.NJS_16_20. Epub 2020 Jul 27.
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.
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 3 postoperative week. Follow-up period was between 1 and 3 years.
All the six patients were free from symptoms postoperatively. Minimal complications were noted in two patients, which were managed conservatively.
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.
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性错构瘤是这种常见肿瘤的变异类型。所有这些变异类型都归类于神经脂肪过多症。这些肿瘤大多数无症状,可进行观察。有症状的患者需要手术治疗,但手术方式并不规范。由于病例数量不足,尚未对纤维脂肪性错构瘤的治疗进行随机对照研究。我们研究的目的是确定纤维脂肪性错构瘤的表现形式、所采用的手术治疗方法以及恢复和并发症形式的治疗结果。
这项回顾性描述性研究纳入了12年间诊断为纤维脂肪性错构瘤的6例患者。从病历中收集患者的详细信息。纳入手部诊断为纤维脂肪性错构瘤的患者。排除患有其他软组织肿瘤的患者。6例患者中,4例需要切除神经,然后使用腓肠神经移植进行重建,2例接受了神经元件的显微手术解剖。指导患者在恢复阶段照顾好手术手。术后第3周开始按照机构物理治疗方案进行治疗。随访期为1至3年。
所有6例患者术后均无症状。2例患者出现轻微并发症,经保守治疗。
对于肘部以下正中神经的纤维脂肪性错构瘤,采用神经解剖或使用腓肠神经移植进行神经重建的手术切除,术后给予适当护理和物理治疗,在我们的研究中已证明对患者有益。