Strauss Christian, Bischoff Barbara, Romstöck Johann, Rachinger Jens, Rampp Stefan, Prell Julian
Department of Neurosurgery, Martin Luther University of Halle-Wittenberg, Halle, Germany.
J Neurosurg. 2008 Jul;109(1):70-6. doi: 10.3171/JNS/2008/109/7/0070.
Vestibular schwannomas (VSs) with no or little extension into the internal auditory canal have been addressed as a clinical subentity carrying a poor prognosis regarding hearing preservation, which is attributed to the initially asymptomatic intracisternal growth pattern. The goal in this study was to assess hearing preservation in patients who underwent surgery for medial VSs.
A consecutive series of 31 cases in 30 patients with medial VSs (mean size 31 mm) who underwent surgery between 1997 and 2005 via a suboccipitolateral route was evaluated with respect to pre- and postoperative cochlear nerve function, extent of tumor removal, and radiological findings. Intraoperative monitoring of brainstem auditory evoked potentials was performed in all patients with hearing. Patients were reevaluated at a mean of 30 months following surgery.
Preoperative hearing function revealed American Academy of Otolaryngology-Head and Neck Surgery Foundation Classes A and B in 7 patients each, Class C in 4, and D in 9. Four patients presented with deafness. Hearing preservation was achieved in 10 patients (Classes A-C in 2 patients each, and Class D in 4 patients). Tumor removal was complete in all patients with hearing preservation, except for 2 patients with neurofibromatosis. In 4 patients a planned subtotal excision was performed due to the individual's age or underlying disease. In 1 patient a recurrent tumor was completely removed 3 years after the initial procedure.
The cochlear nerve in medial VSs requires special attention due to the atypical intracisternal growth pattern. Even in large tumors, hearing could be preserved in 37% of cases, since the cochlear nerve in medial schwannomas may not exhibit the adherence to the tumor capsule seen in tumors with comparable size involving the internal auditory canal.
未向或仅少量向内耳道延伸的前庭神经鞘瘤(VSs)被视为一种临床亚实体,在听力保留方面预后较差,这归因于其最初无症状的脑池内生长模式。本研究的目的是评估接受内侧VSs手术患者的听力保留情况。
对1997年至2005年间通过枕下外侧入路接受手术的30例内侧VSs患者(共31例,平均大小31mm)进行连续研究,评估术前和术后的蜗神经功能、肿瘤切除范围及影像学表现。所有有听力的患者均进行术中脑干听觉诱发电位监测。患者在术后平均30个月时进行复查。
术前听力功能显示,美国耳鼻咽喉头颈外科学会基金会分级中,A类和B类各7例,C类4例,D类9例。4例患者表现为耳聋。10例患者实现了听力保留(其中A-C类各2例,D类4例)。除2例神经纤维瘤病患者外,所有听力保留患者的肿瘤均完全切除。4例患者因年龄或基础疾病进行了计划中的次全切除。1例患者在初次手术后3年将复发性肿瘤完全切除。
由于内侧VSs具有非典型的脑池内生长模式,蜗神经需要特别关注。即使在大型肿瘤中,37%的病例仍可保留听力,因为内侧神经鞘瘤中的蜗神经可能不像累及内耳道的同等大小肿瘤那样与肿瘤包膜粘连。