Medina Perez M, Rafel Ribas E, Valero Puerta J A, Perez Martín D
Servicio de Anatomica Patológica, Hospital de la Merced, Osuna, Sevilla, España.
Arch Esp Urol. 2000 Sep;53(7):634-6.
To report on a rare case of Pacinian neurofibroma of the vulva.
A 27-year-old patient who presented with a vulvar tumor is described. Patient evaluation showed no other remarkable findings.
The nodule was resected without difficulty. The histopathological analysis-demonstrated Pacinian neurofibroma with abundant concentric laminar structures. The immunohistochemical (CD34+), ultrastructural and histological analyses showed perineural cells. No signs of neurofibromatosis were found.
Pacinian neurofibroma may present in the vulva and could probably arise from the so-called perineural fibroblasts.
报告1例罕见的外阴帕西尼神经纤维瘤病例。
描述了1例出现外阴肿物的27岁患者。患者评估未发现其他显著异常。
结节顺利切除。组织病理学分析显示为具有丰富同心层状结构的帕西尼神经纤维瘤。免疫组织化学(CD34阳性)、超微结构和组织学分析显示有神经周细胞。未发现神经纤维瘤病迹象。
帕西尼神经纤维瘤可出现在外阴,可能起源于所谓的神经周成纤维细胞。