LARGE SOLITARY ENCAPSULATED NEUROFIBROMA OF UPPER ARM – A CASE REPORT

Sanamed Pub Date : 2022-06-02 DOI:10.5937/sanamed17-36810
Z. Terzić, Dubravka Radonjic, M. Paunović, A. Ljaljević, Miloš Bojić
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引用次数: 1

Abstract

Introduction: Neurofibromas are benign tumors of neuronal origin, occurring most commonly in young adults, with no gender predilection. The connection of neurofibroma with disorders on a general level as von Recklinghausen’s disease makes its diagnosis critical. Case report: A 32-old female patient was administered to the Clinic of Plastic surgery, Clinical Center of Montenegro in Podgorica, with a 10-year history of painless, subcutaneous tumor of the right upper arm that grew in size over the last ten years. The patient reported progressive pain and tingling in her right forearm and right hand for the last 12 months. An MRI showed a non-homogenous tumor of the middle third portion of the triceps muscle, in close contact with the humerus but without infiltrating it. The tumor was removed, with a definitive histopathological result of a solitary benign neurofibroma. Conclusions: This example of successful treatment of solitary neurofibroma may serve to increase the awareness of surgeons and radiologists in small countries regarding benign peripheral nerve sheath tumors. The patient is under observation for two years with no signs of relapse and no other features indicative of neurofibromatosis type 1.
上臂大孤立性包膜神经纤维瘤1例
简介:神经纤维瘤是神经元起源的良性肿瘤,最常见于年轻人,无性别偏好。神经纤维瘤与von Recklinghausen病等一般疾病的联系使其诊断至关重要。病例报告:一名32岁的女性患者被送往波德戈里察黑山临床中心整形外科诊所,她有10年的右上臂无痛皮下肿瘤病史,在过去10年中肿瘤不断扩大。患者报告称,在过去的12个月里,她的右前臂和右手出现了渐进性疼痛和刺痛。核磁共振成像显示三头肌中三分之一的非均质肿瘤,与肱骨密切接触,但没有浸润。肿瘤被切除,明确的组织病理学结果为孤立的良性神经纤维瘤。结论:这个成功治疗孤立性神经纤维瘤的例子可能有助于提高小国外科医生和放射科医生对良性周围神经鞘肿瘤的认识。该患者接受了两年的观察,没有复发的迹象,也没有其他表明1型神经纤维瘤病的特征。
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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