Pereira Marcelo Charles, Peris-Celda Maria, Qian Jiang, Kenning Tyler J, Pinheiro-Neto Carlos D
Division of Otolaryngology/Head and Neck Surgery, Department of Surgery, Albany Medical Center, Albany, New York.
Department of Neurosurgery, Albany Medical Center, Albany, New York.
World Neurosurg. 2016 May;89:729.e15-20. doi: 10.1016/j.wneu.2016.01.050. Epub 2016 Feb 4.
Olfactory schwannomas of the anterior cranial base (ACB) are rare tumors, and their association with hereditary hemorrhagic telangiectasia (HHT) has not previously been described. The majority of ACB schwannomas arise from the sinonasal tracts and may demonstrate intracranial extension. We report a case of an olfactory schwannoma-dense adherence to the basal frontal lobe. Complete tumor resection was performed through a unilateral extended endonasal endoscopic approach with preservation of the contralateral olfactory bulb. Anterior cranial base repair was achieved with the use of a mucoperichondrial vascularized pedicled nasoseptal flap.
A 25-year-old woman with a history of migraines presented with unilateral epistaxis and progressive worsening of her headache symptoms. The patient had a history of HHT. Nasal endoscopy showed mild telangiectasias, but no clear evidence of a mass. A computerized tomographic scan showed a large left-sided expansile lesion in the left ethmoid region with expansion and remodeling of the anterior cranial base and medial left orbit. Magnetic resonance imaging with contrast showed the mass to be avidly enhancing. Angiography was performed and demonstrated a mild vascular blush.
We report a rare case of HTT and olfactory schwannoma completely resected with a unilateral extended endoscopic endonasal approach. Reconstruction was performed with the use of nasoseptal flap. This is the first reported single-stage fully endoscopic endonasal unilateral approach for resection of an olfactory schwannoma with preservation of the contralateral olfactory cleft. The patient's sense of smell and taste was maintained after surgery.
前颅底嗅神经鞘瘤是罕见肿瘤,此前尚未有其与遗传性出血性毛细血管扩张症(HHT)相关的描述。大多数前颅底神经鞘瘤起源于鼻窦道,可能会向颅内扩展。我们报告一例与额叶底部紧密粘连的嗅神经鞘瘤病例。通过单侧扩大经鼻内镜入路完整切除肿瘤,同时保留对侧嗅球。采用带蒂鼻中隔黏骨膜瓣修复前颅底。
一名有偏头痛病史的25岁女性出现单侧鼻出血,头痛症状逐渐加重。该患者有HHT病史。鼻内镜检查显示轻度毛细血管扩张,但无明显肿物迹象。计算机断层扫描显示左侧筛窦区有一个大的左侧膨胀性病变,前颅底和左侧眼眶内侧有扩张和重塑。增强磁共振成像显示肿物明显强化。进行了血管造影,显示有轻度血管造影剂外渗。
我们报告了一例罕见的HHT合并嗅神经鞘瘤病例,通过单侧扩大经鼻内镜入路完全切除肿瘤。采用鼻中隔瓣进行重建。这是首次报道的单阶段完全经鼻内镜单侧入路切除嗅神经鞘瘤并保留对侧嗅裂的病例。术后患者嗅觉和味觉得以保留。