Shkarubo A N, Lubnin A Yu, Bukharin E Yu, Shishkina L V, Andreev D N, Koval' K V, Chernov I V, Karnaukhov V V
Burdenko Neurosurgical Institute, Moscow, Russia.
Zh Vopr Neirokhir Im N N Burdenko. 2017;81(1):81-87. doi: 10.17116/neiro201780781-87.
An extended endoscopic endonasal approach is increasingly used in surgical treatment of space-occupying skull base lesions. The international literature reports only 20 cases of surgical treatment for fibrous dysplasia (PD) of the skull base using the endoscopic endonasal approach. We present our experience with the endoscopic endonasal approach in surgical treatment for giant fibrous dysplasia of the skull base, spreading to the right orbital cavity and nasopharynx.
A 26-year-old male patient presented with cranial pain, Vth nerve dysfunction on the right, right keratopathy. OD=0.2 (near acuity - 0.3), OS=1.0, OD - incomplete eyelid closure of 2 mm, conjunctival injection, mucous discharge, corneal opacity in the lower pole and paracentrally, OS - normal appearance. Severe right-sided exophthalmos (more than 15 mm), impaired nasal breathing on the right, nasal (hemorrhagic) discharge. Magnetic resonance imaging and spiral computed tomography scans revealed a bone density lesion located in the area of the orbit, nasal cavity, maxillary sinus on the right, and labyrinth of the ethmoid bone. The patient underwent endonasal endoscopic resection of the lesion.
The lesion was resected totally, which was confirmed by control SCT. Right-sided exophthalmos partially regressed (on the right: exophthalmos of 8 mm; protrusion: OD=23 mm, OS=15 mm; the eyeball was displaced downward and outward). The visual and oculomotor functions did not change. The neurological status remained at the preoperative level.
Fibrous dysplasia of the skull base is an extremely rare disease. Modern techniques expand the indications for surgery of giant tumors of the skull base using minimally invasive approaches, in particular the endoscopic endonasal approach.
扩大经鼻内镜入路越来越多地用于颅底占位性病变的手术治疗。国际文献仅报道了20例采用经鼻内镜入路手术治疗颅底骨纤维异常增殖症(FD)的病例。我们介绍了经鼻内镜入路手术治疗累及右侧眶腔和鼻咽部的巨大颅底骨纤维异常增殖症的经验。
一名26岁男性患者,主诉头痛、右侧Ⅴ神经功能障碍、右侧角膜病变。右眼视力=0.2(近视力-0.3),左眼视力=1.0,右眼不完全眼睑闭合2mm,结膜充血、有分泌物,下角膜及旁中央角膜混浊,左眼外观正常。右侧严重眼球突出(超过15mm),右侧鼻呼吸障碍,有鼻(血性)分泌物。磁共振成像和螺旋计算机断层扫描显示右侧眼眶、鼻腔、上颌窦及筛骨迷路区域有骨质密度病变。患者接受了经鼻内镜下病变切除术。
病变被完全切除,术后CT检查证实。右侧眼球突出部分消退(右侧:眼球突出8mm;突出度:右眼=23mm,左眼=15mm;眼球向下和向外移位)。视觉和动眼功能未改变。神经状态维持在术前水平。
颅底骨纤维异常增殖症是一种极其罕见的疾病。现代技术扩大了采用微创方法,特别是经鼻内镜入路手术治疗巨大颅底肿瘤的适应证。