Soldado L, Solanellas J, Esteban F
Hospital Universitario Virgen de Valme, Sevilla, España.
An Otorrinolaringol Ibero Am. 1997;24(4):415-24.
Type 2 neurofibromatosis is a rare genetic condition, with an autosomal (dominant) inheritance and a prevalence of 1/50.000 inhabitants, characterized by bilateral acoustic neuromas. We present here a 16-year-old patient with a greater growth of the right-sided neuroma. A review of the literature, regarding incidence, clinical presentation, diagnostic clues and treatment is also included.
2型神经纤维瘤病是一种罕见的遗传性疾病，呈常染色体（显性）遗传，患病率为1/50000居民，其特征为双侧听神经瘤。我们在此报告一名16岁患者，其右侧神经瘤生长更为明显。本文还包括对发病率、临床表现、诊断线索及治疗的文献综述。
