Kiratli Hayyam, Yildiz Sibel, Soylemezoğlu Figen
Department of Ophthalmology, Hacettepe University School of Medicine, Ankara, Turkey.
Orbit. 2008;27(6):451-4. doi: 10.1080/01676830802350356.
A highly unusual patient with neurofibromatosis type 2 (NF2) presenting with simultaneous bilateral orbital tumors is described. A 12-year-old girl with a family history of NF2 was examined because of bilateral proptosis. Visual acuities were light perception RE and 20/40 LE. Magnetic resonance imaging studies showed bilateral cerebellopontine angle tumors, a tumor surrounding the right intraorbital optic nerve, and a large left lateral orbital mass mixed with the lateral rectus muscle. The histopathological diagnoses following incisional biopsies were right optic nerve sheath meningioma and left intramuscular schwannoma. The left-sided orbital schwannoma and the right-sided vestibular schwannoma were treated with fractionated stereotactic radiotherapy. This patient enlarges the spectrum of clinical presentations that can be encountered at young age in patients with NF2.
本文描述了一名极为罕见的2型神经纤维瘤病(NF2)患者,该患者同时出现双侧眼眶肿瘤。一名有NF2家族病史的12岁女孩因双侧眼球突出接受检查。右眼视力为光感,左眼视力为20/40。磁共振成像研究显示双侧桥小脑角肿瘤、围绕右侧眶内视神经的肿瘤以及与左侧外直肌混合的巨大左侧眶外侧肿块。切开活检后的组织病理学诊断为右侧视神经鞘膜瘤和左侧肌内神经鞘瘤。左侧眼眶神经鞘瘤和右侧前庭神经鞘瘤接受了分次立体定向放射治疗。该患者扩展了NF2患者在年轻时可能出现的临床表现谱。