一例孤立性神经纤维瘤累及一个年轻的部落女孩的下肢

Alisha Kalyanpur, Royson Dsouza, B. Kurien
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引用次数: 0

摘要

我们描述了一位17岁的女孩,她表现为右腿非创伤性逐渐进行性肿胀2个月。临床表现为弥漫性肿胀,累及右腿外侧的下三分之一,肿胀牢固且无压痛。其他地方没有类似的肿胀。放射检查结果不确定,她接受了切除活检。组织病理学表现为神经纤维瘤特征。下肢孤立性神经纤维瘤是极为罕见的良性病变,具有非特异性的临床和影像学特征。组织病理学是诊断的主要依据。广泛的局部切除是强制作为治疗,因为这些病变有复发的倾向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of solitary neurofibroma involving the lower limb in a young tribal girl
We describe a 17-year-old girl who presented with a nontraumatic gradually progressive swelling in the right leg for 2 months. Clinically, there was a diffuse swelling involving the lower third of the lateral aspect of the right leg, which was firm and nontender. There were no similar swellings elsewhere. The radiological findings were inconclusive and she underwent an excision biopsy. Histopathology revealed features consistent with a neurofibroma. Solitary neurofibromas of the lower extremity are extremely rare benign lesions, having nonspecific clinical and radiological features. Histopathology is the mainstay of the diagnosis. Wide local resection is mandated as the treatment as these lesions have a propensity for recurrence.
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