Elliott F G, Eid T C, Lakey W H
J Urol. 1981 May;125(5):725-7. doi: 10.1016/s0022-5347(17)55181-2.
We describe 2 unusual cases of genitourinary neurofibromas. In 1 case a large solitary neurofibroma developed on the glans penis and in the other case a plexiform neurofibroma of the pelvis was present in young women with von Recklinghausen's disease. Each case represents either end of the spectrum of urologic involvement by this rare tumor. The solitary neurofibroma requires only local excision but the plexiform neurofibroma, causing urinary obstruction, necessitates urinary diversion. Recurrence and malignant degeneration, while virtually unheard of in the former, are relatively common in the latter. The prognosis of each type is discussed.
我们描述了2例不寻常的泌尿生殖系统神经纤维瘤病例。1例为阴茎头出现一个大的孤立性神经纤维瘤,另1例为一名患有冯·雷克林豪森病的年轻女性盆腔出现丛状神经纤维瘤。每个病例都代表了这种罕见肿瘤在泌尿系统累及范围的两端。孤立性神经纤维瘤仅需局部切除,但丛状神经纤维瘤导致尿路梗阻,则需要进行尿流改道。复发和恶性变在前者几乎闻所未闻,而在后者则相对常见。文中讨论了每种类型的预后。