Chiu F Y, Chen T H, Shih L Y, Lo W H
Department of Orthopedics and Traumatology, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1993 Nov;52(5):346-50.
Multiple glomus tumor (MGT) is rare in incidence. A 37-year-old male was diagnosed to have localized MGT over his right leg. With the characteristics of unusual location (right lower leg), development in sequence, and distribution along the course of the lateral sural cutaneous nerve. Its pathological findings were also characteristic. When the overall presentations showed in cases with recurrent symptoms and signs of glomus tumor after surgical excision, recurrence and multiplicity should be considered.
多发型血管球瘤发病率罕见。一名37岁男性被诊断为右下肢局限性多发型血管球瘤。其具有位置特殊（右小腿）、依次发展且沿腓肠外侧皮神经走行分布的特点。其病理表现也具有特征性。当病例出现手术切除后血管球瘤复发的症状和体征时，应考虑复发和多发性的情况。
