Grahnke Kurt, Burkett Daniel, Li Daphne, Szujewski Caroline, Leonetti John P, Anderson Douglas E
Departments of Neurological Surgery and Otolaryngology, Head and Neck Surgery, and Stritch School of Medicine, Loyola University Chicago, Health Sciences Campus, Maywood, Illinois, United States.
Department of Neurological Surgery, University of Wisconsin Hospitals and Clinics, Madison, Wisconsin, United States.
J Neurol Surg B Skull Base. 2018 Oct;79(5):445-450. doi: 10.1055/s-0037-1617431. Epub 2018 Jan 9.
Epidermoid cysts are rare lesions, accounting for 0.2 to 1.8% of all intracranial tumors. They most commonly occur in the cerebellopontine angle where they may cause a breadth of neurologic complications due to mass effect on the nearby cranial nerves (CN), vascular structures, and the brain stem. Treatment of epidermoid cysts is surgical, with the goal of complete resection using microsurgical technique and even more importantly preservation of the involved CNs, vasculature, and brain parenchyma. Successful surgery can result in total resolution of symptoms, but, in certain situations, may not be advisable due to adherence, scarring, or inflammation making dissection of CN fascicles difficult and possibly hazardous. We conducted a retrospective review from 1998 to 2016 and compiled a series of 28 skull base epidermoid cysts operated on at our institution. Cases were evaluated for presenting symptoms, history of prior resection, and postoperative results including CN function, extent of resection, residual tumor, and need for reoperations. The average tumor size (largest diameter) was 3.9 cm with a range of 1 to 7cm. Eighteen of twenty-eight (64%) patients underwent a gross total resection and ten underwent subtotal resection. No patients, whether presenting with CN deficits or not, experienced permanent worsening of CN function following surgery. Complete resection of epidermoid cysts should remain a high priority of therapy, but, in our opinion, preservation of CN function should be a primary goal, determining the extent of resection to provide patients with the highest quality of life possible following surgery.
表皮样囊肿是罕见病变,占所有颅内肿瘤的0.2%至1.8%。它们最常发生在桥小脑角,由于对附近颅神经(CN)、血管结构和脑干的占位效应,可能导致多种神经并发症。表皮样囊肿的治疗方法是手术,目标是使用显微外科技术完全切除,更重要的是保留受累的颅神经、脉管系统和脑实质。成功的手术可使症状完全缓解,但在某些情况下,由于粘连、瘢痕形成或炎症导致颅神经束分离困难且可能有危险,手术可能不可取。我们对1998年至2016年进行了回顾性研究,并汇总了在我们机构接受手术的28例颅底表皮样囊肿病例。对病例进行了评估,包括出现的症状、既往切除史以及术后结果,如颅神经功能、切除范围、残留肿瘤和再次手术的必要性。平均肿瘤大小(最大直径)为3.9厘米,范围为1至7厘米。28例患者中有18例(64%)接受了全切除,10例接受了次全切除。无论术前是否存在颅神经功能缺损,所有患者术后均未出现颅神经功能永久性恶化。表皮样囊肿的完全切除应始终是治疗的重中之重,但我们认为,保留颅神经功能应是主要目标,它决定了切除范围,以便为患者提供术后尽可能高的生活质量。