Malone James P, Lee Wha-Joon, Levin Roger J
Division of Otolaryngology-Head and Neck Surgery, Penn State University College of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA 17033, USA.
Am J Otolaryngol. 2005 Mar-Apr;26(2):108-12. doi: 10.1016/j.amjoto.2004.08.011.
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.
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.
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%).
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.
由于涉及该区域的病变会带来相关发病率,涉及头颈部神经鞘瘤的研究主要集中在前庭蜗神经复合体(听神经瘤)。然而,大多数头颈部神经鞘瘤并非起源于前庭神经,由于眼眶、颅底和颅神经受累,也可能导致显著的发病率。本研究的目的是检查头颈部非前庭神经鞘瘤患者的临床表现、位置、起源神经以及治疗后的结果。
回顾性分析了1979年至1999年在单一机构接受治疗的所有头颈部非前庭神经鞘瘤患者的医学和病理记录。
26例患者中有18例(69%)出现因占位效应或神经功能缺损引起的症状。咽旁间隙是最常见的肿瘤起源部位,有8例患者(31%)。16例患者(62%)确定了起源神经。23例患者(88%)接受了完整的手术切除,3例患者(12%)接受了次全切除。16例患者(62%)发生术后神经损伤,7例患者(44%)症状缓解。
头颈部非前庭神经鞘瘤最常发生于咽旁间隙,临床表现通常与占位效应或神经功能缺损有关。通常能够实现肿瘤的完整切除,但对于颅底、中耳或面神经广泛受累的患者,可能需要进行次全或近全切除。术后发病率与手术入路和/或受累神经切除导致的神经损伤有关。