Cebesoy Oguz, Tutar Ediz, Isik Mustafa, Arpacioglu Omer
Orthopedic and Traumatology Department, Gaziantep University Faculty of Medicine, 27060 Gaziantep, Turkey.
Arch Orthop Trauma Surg. 2007 Oct;127(8):709-12. doi: 10.1007/s00402-007-0303-1. Epub 2007 Mar 22.
Plexiform neurofibroma is generally considered as a component of neurofibromatosis 1, and a great majority of the cases with plexiform neurofibroma display other symptoms related to neurofibromatosis. Plexiform neurofibromas occur frequently in the head and neck region due to the rich innervation of the area, however appear rarely in the extremities. We report here an isolated giant plexiform neurofibroma involving the common peroneal nerve branches without symptoms related to neurofibromatosis in a 5-year-old case. Surgical excision was performed due to pain and numbness in the leg, and against the possibility of malignant transformation due to sudden growth observed in the tumor. One month following the excision of all the reachable tumoral tissues, tendon transfer surgery was performed for the ankle and toe extensions. Our case stands as the only reported case of isolated giant plexiform neurofibroma involving the common peroneal nerve in the pediatric age.
丛状神经纤维瘤通常被认为是神经纤维瘤病1型的一个组成部分,绝大多数患有丛状神经纤维瘤的病例还表现出与神经纤维瘤病相关的其他症状。由于头颈部区域神经分布丰富,丛状神经纤维瘤在该区域频繁发生,但在四肢很少出现。我们在此报告一例5岁患儿,其孤立性巨大丛状神经纤维瘤累及腓总神经分支,且无神经纤维瘤病相关症状。由于腿部疼痛和麻木,以及考虑到肿瘤突然生长有恶变的可能性,遂进行了手术切除。在切除所有可触及的肿瘤组织一个月后,为恢复踝关节和足趾伸展功能进行了肌腱转移手术。我们的病例是唯一报道的小儿孤立性巨大丛状神经纤维瘤累及腓总神经的病例。