Borba Luis A B, Ale-Bark Samir, London Charles
Department of Neurosurgery, Center for Neurological Surgery of Parana, Evangelical University Medical School, Curitiba, Parana, Brazil.
Neurosurg Focus. 2004 Aug 15;17(2):E8. doi: 10.3171/foc.2004.17.2.8.
Glomus jugulare tumors are benign lesions located in the jugular foramen that may or may not extend into the middle ear, petrous apex, and upper neck; these growths sometimes invade intradurally. The surgical management of these tumors is a challenge to neurosurgeons and skull base surgeons. Because of their abundant vascularity, deep location, complex anatomy, and difficult surgical approach, their treatment, has been a controversial issue for many years. Despite advancements in nonsurgical techniques, the only treatment with proven efficacy is radical surgical removal. The authors present a series of patients treated with radical removal, in which the feasibility of removing glomus jugulare tumors with low morbidity and a surgical approach limited to tumor removal are discussed. The extent of surgical exposure is tailored with emphasis placed on the routine anterior transposition of the facial nerve.
Between May 1997 and March 2004, 24 patients with glomus jugulare tumors were treated; 17 patients were women and seven were men. Their mean age at the time of diagnosis was 50 years (range 18-71 years). The most common symptom was hearing loss in 77%, followed by dysphagia and dysphonia in 55% of patients. In seven patients the clinical presentation was a facial palsy. Radical tumor removal was achieved in 23 patients. An anterior facial nerve transposition was not needed in any case. No surgery-related death was recorded in this series, although one patient died of a pulmonary embolism 70 days after the procedure. A one-stage procedure was performed in 23 patients and a two-stage procedure was used in the other patient. Cerebrospinal fluid leakage occurred in two patients. The lower cranial nerve function was worse in eight patients; however, only one had a new deficit. The facial nerve was preserved in all patients except one, in whom a large intradural tumor caused a temporary facial palsy. In the patients with preoperative facial palsy, the tumor only compressed the nerve in three and it invaded the nerve in four. The nerve was decompressed in the cases with no invasion and a graft was placed in the others. The greater auricular nerve was used as a graft in three and the sural nerve was used in one. On follow-up review, the facial nerve function was House-Brackmann Grade 3 in three patients and Grade 2 in three. After 6 months of follow up with no improvement, one patient was referred for a facial muscle transfer.
The surgical technique must be tailored to each case. The authors believe that the standard surgical approach to jugular foramen tumors with anterior transposition of the facial nerve should be avoided, and that the extent of surgical exposure must be tailored to each case based on the extent of the tumor and the clinical symptoms. Lower morbidity rates and radical removal can be achieved with a good surgical plan.
颈静脉球瘤是位于颈静脉孔的良性病变,可延伸至中耳、岩尖和上颈部,也可不延伸;这些肿瘤有时会侵犯硬膜内。对神经外科医生和颅底外科医生来说,这些肿瘤的手术治疗是一项挑战。由于其血管丰富、位置深、解剖结构复杂且手术入路困难,多年来其治疗一直是一个有争议的问题。尽管非手术技术有所进步,但唯一经证实有效的治疗方法是根治性手术切除。作者介绍了一系列接受根治性切除治疗的患者,讨论了以低发病率切除颈静脉球瘤以及仅限于肿瘤切除的手术入路的可行性。手术暴露范围根据具体情况进行调整,重点是面神经的常规前移。
1997年5月至2004年3月,对24例颈静脉球瘤患者进行了治疗;其中17例为女性,7例为男性。诊断时的平均年龄为50岁(范围18 - 71岁)。最常见的症状是听力丧失,占77%,其次是吞咽困难和发音困难,占55%。7例患者临床表现为面瘫。23例患者实现了肿瘤的根治性切除。无一例需要进行面神经前移。本系列中未记录到与手术相关的死亡,尽管有1例患者在术后70天死于肺栓塞。23例患者采用一期手术,另1例采用二期手术。2例患者发生脑脊液漏。8例患者的低位颅神经功能较差;然而,只有1例出现了新的功能缺损。除1例因硬膜内大肿瘤导致暂时性面瘫外,所有患者的面神经均得以保留。在术前有面瘫的患者中,3例肿瘤仅压迫神经,4例肿瘤侵犯神经。未受侵犯的病例中神经得到减压,其他病例则进行了神经移植。3例使用耳大神经作为移植神经,1例使用腓肠神经。随访复查时,3例患者的面神经功能为House - Brackmann 3级,3例为2级。随访6个月无改善后,1例患者接受了面肌转移术。
手术技术必须根据具体病例进行调整。作者认为,应避免采用面神经前移的标准手术入路治疗颈静脉孔肿瘤,手术暴露范围必须根据肿瘤范围和临床症状针对每个病例进行调整。制定良好的手术计划可实现较低的发病率和根治性切除。