Radial nerve myofibroma: a rare benign tumor with perineural infiltration. Illustrative case.

Kitty Y Wu, David J Cook, Kimberly K Amrami, Robert J Spinner
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Abstract

Background: Myofibromas are benign mesenchymal tumors, classically presenting in infants and young children in the head and neck region. Perineural involvement, especially in peripheral nerves within the upper extremity, is extremely rare in myofibromas.

Observations: The authors present the case of a 16-year-old male with a 4-month history of an enlarging forearm mass and rapidly progressive dense motor weakness in wrist, finger, and thumb extension. Preoperative imaging and fine needle biopsy confirmed the diagnosis of a benign isolated myofibroma. Given the dense paralysis, operative management was indicated, and intraoperative exploration showed extensive involvement of tumor within the radial nerve. The infiltrated nerve segment was excised along with the tumor, and the resulting 5-cm nerve gap was reconstructed using autologous cabled grafts.

Lessons: Perineural pseudoinvasion can be an extremely rare and atypical feature of nonmalignancies, resulting in dense motor weakness. Extensive nerve involvement may still necessitate nerve resection and reconstruction, despite the benign etiology of the lesion.

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桡神经肌原纤维瘤:一种罕见的伴有神经周围浸润的良性肿瘤。说明性案例。
背景:肌纤维瘤是一种良性间充质肿瘤,常见于婴幼儿头颈部。周围神经受累,尤其是上肢周围神经,在肌纤维瘤中极为罕见。观察结果:作者报告了一名16岁男性的病例,他有4个月的前臂肿块增大和手腕、手指和拇指伸展快速进行性密集运动无力的病史。术前影像学和细针活检证实诊断为良性孤立性肌原纤维瘤。考虑到密集性麻痹,需要手术治疗,术中探查显示肿瘤广泛累及桡神经。将浸润的神经段与肿瘤一起切除,并使用自体电缆移植物重建由此产生的5cm神经间隙。经验教训:神经周假性侵犯可能是一种极为罕见和非典型的非恶性特征,导致密集性运动无力。广泛的神经受累可能仍然需要神经切除和重建,尽管病变的病因是良性的。
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