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Clinical characteristics and treatment outcome for nonvestibular schwannomas of the head and neck.

机译:头颈部非前庭神经鞘瘤的临床特征和治疗结果。

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Abstract Purpose Studies involving head and neck schwannomas have focused predominantly on involvement of the vestibulocochlear nerve complex (acoustic neuroma) because of the associated morbidity related to lesions involving that region. However, the majority of head and neck schwannomas are not of vestibular nerve origin and may also produce significant morbidity due to involvement of the orbit, skull base, and cranial nerves. The purpose of this study is to examine the presenting signs and symptoms, location, nerve of origin, and outcome after treatment of patients with nonvestibular schwannomas of the head and neck. Materials and methods The medical and pathological records of all patients with nonvestibular head and neck schwannomas treated at a single institution between 1979 and 1999 were retrospectively reviewed. Results Eighteen (69%) of 26 patients presented with symptoms secondary to mass effect or nerve deficit. The parapharyngeal space was the most common site of tumor origin occurring in 8 patients (31%). The nerve of origin was identified in 16 patients (62%). Twenty-three patients (88%) had complete surgical excision, and 3 patients (12%) had subtotal resection. Postoperative nerve injury occurred in 16 patients (62%) with resolution in 7 patients (44%). Conclusions Nonvestibular head and neck schwannomas occur most commonly in the parapharyngeal space, and presenting signs or symptoms are usually related to mass effect or neural deficit. Complete tumor removal is often achieved, but subtotal or near-total resection may be indicated for patients with extensive skull base, middle ear, or facial nerve involvement. Postoperative morbidity is associated with nerve injury from the surgical approach and/or resection of the involved nerve.
机译:摘要目的涉及头颈部神经鞘瘤的研究主要集中在前庭耳蜗神经复合体(听神经瘤)的介入,因为与该区域病变相关的发病率很高。但是,大多数头颈部神经鞘瘤不是起源于前庭神经,并且由于眶,颅底和颅神经的参与,也可能产生大量发病。这项研究的目的是检查头颈部非前庭神经鞘瘤患者治疗后的体征和症状,位置,起源神经和结局。资料与方法回顾性分析了1979年至1999年在同一机构接受治疗的所有非前庭头颈部神经鞘瘤的患者的医学和病理记录。结果26例患者中有18例(69%)表现为继发于质量效应或神经缺陷的症状。咽旁间隙是8例患者中最常见的肿瘤起源部位(31%)。 16例患者中有起源神经(62%)。 23例(88%)已完成手术切除,3例(12%)进行了大体切除。术后神经损伤发生在16例患者(62%)中,而在7例患者中(44%)消退。结论非前庭头颈部神经鞘瘤多见于咽旁间隙,其体征或症状通常与质量效应或神经功能缺损有关。通常可以实现完全的肿瘤切除,但是对于颅底广泛,中耳或面神经受累的患者,可能需要进行次全切除或近全切除。术后发病与手术方法和/或受累神经切除引起的神经损伤有关。

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