Cunningham Calhoun D, Friedman Rick A, Brackmann Derald E, Hitselberger William E, Lin Harrison W
House Ear Clinic and House Ear Institute, Los Angeles, California, USA.
Otol Neurotol. 2005 Mar;26(2):231-6. doi: 10.1097/00129492-200503000-00017.
Innovations in diagnosis, surgical techniques, and perioperative care have dramatically improved outcomes in lateral skull base procedures in recent years. There is a belief, however, that children with skull base tumors have yet to benefit from these technological and procedural advances. The purpose of this study is to provide a clinical review of neurotologic skull base surgery in the pediatric population.
Retrospective case review.
Private practice tertiary referral center.
Eighty-nine pediatric patients undergoing 115 neurotologic procedures for lateral skull base tumors from July 1992 to September 2003.
Initial clinical presentation, tumor type, pre- and postoperative hearing and facial nerve status, treatment course, complications, and functional outcomes.
The majority of tumors in this series were vestibular schwannomas, and 65 patients were diagnosed with neurofibromatosis Type 2. Surgical approaches included 70 middle fossa, 40 translabyrinthine, 2 transcochlear, 2 infratemporal fossa, and 1 retrosigmoid craniotomy. Complete tumor removal was accomplished in the majority of cases (97%), with good preservation of facial nerve function (House-Brackmann Grade I or II) in 80% of patients. In patients undergoing middle fossa surgery for hearing preservation, measurable hearing was preserved in 61.4% of cases. The incidence of complications was low.
With advances in diagnostic procedures and use of current neurotologic techniques, pediatric patients may undergo successful treatment of lateral skull base tumors, with good functional outcomes and minimal morbidity.
近年来,诊断、手术技术及围手术期护理方面的创新显著改善了侧颅底手术的疗效。然而,有一种观点认为,患有颅底肿瘤的儿童尚未从这些技术和手术进展中获益。本研究的目的是对儿科患者的神经耳科颅底手术进行临床综述。
回顾性病例分析。
私立三级转诊中心。
1992年7月至2003年9月期间,89例儿科患者接受了115例针对侧颅底肿瘤的神经耳科手术。
初始临床表现、肿瘤类型、术前和术后听力及面神经状况、治疗过程、并发症及功能结局。
本系列中的大多数肿瘤为前庭神经鞘瘤,65例患者被诊断为2型神经纤维瘤病。手术入路包括70例中颅窝入路、40例迷路后入路、2例经耳蜗入路、2例颞下窝入路和1例乙状窦后开颅术。大多数病例(97%)实现了肿瘤完全切除,80%的患者面神经功能得到良好保留(House-Brackmann Ⅰ级或Ⅱ级)。在接受中颅窝手术以保留听力的患者中,61.4%的病例保留了可测量的听力。并发症发生率较低。
随着诊断程序的进步和当前神经耳科技术的应用,儿科患者可以成功治疗侧颅底肿瘤,获得良好的功能结局且并发症最少。