Ramina Ricardo, Maniglia Joao Jarney, Fernandes Yvens Barbosa, Paschoal Jorge Rizzato, Pfeilsticker Leopoldo Nizan, Neto Mauricio Coelho, Borges Guilherme
Neurosurgery Department of Instituto de Neurologia de Curitiba, Brazil.
Neurosurg Focus. 2004 Aug 15;17(2):E5. doi: 10.3171/foc.2004.17.2.5.
Jugular foramen tumors are rare skull base lesions that present diagnostic and complex management problems. The purpose of this study was to evaluate a series of patients with jugular foramen tumors who were surgically treated in the past 16 years, and to analyze the surgical technique, complications, and outcomes.
The authors retrospectively studied 102 patients with jugular foramen tumors treated between January 1987 and May 2004. All patients underwent surgery with a multidisciplinary method combining neurosurgical and ear, nose, and throat techniques. Preoperative embolization was performed for paragangliomas and other highly vascularized lesions. To avoid postoperative cerebrospinal fluid (CSF) leakage and to improve cosmetic results, the surgical defect was reconstructed with specially developed vascularized flaps (temporalis fascia, cervical fascia, sternocleidomastoid muscle, and temporalis muscle). A saphenous graft bypass was used in two patients with tumor infiltrating the internal carotid artery (ICA). Facial nerve reconstruction was performed with grafts of the great auricular nerve or with 12th/seventh cranial nerve anastomosis. Residual malignant and invasive tumors were irradiated after partial removal. The most common tumor was paraganglioma (58 cases), followed by schwannomas (17 cases) and meningiomas (10 cases). Complete excision was possible in 45 patients (77.5%) with paragangliomas and in all patients with schwannomas. The most frequent and also the most dangerous surgical complication was lower cranial nerve deficit. This deficit occurred in 10 patients (10%), but it was transient in four cases. Postoperative facial and cochlear nerve paralysis occurred in eight patients (8%); spontaneous recovery occurred in three of them. In the remaining five patients the facial nerve was reconstructed using great auricular nerve grafts (three cases), sural nerve graft (one case), and hypoglossal/facial nerve anastomosis (one case). Four patients (4%) experienced postoperative CSF leakage, and four (4.2%) died after surgery. Two of them died of aspiration pneumonia complicated with septicemia. Of the remaining two, one died of pulmonary embolism and the other of cerebral hypoxia caused by a large cervical hematoma that led to tracheal deviation.
Paragangliomas are the most common tumors of the jugular foramen region. Surgical management of jugular foramen tumors is complex and difficult. Radical removal of benign jugular foramen tumors is the treatment of choice, may be curative, and is achieved with low mortality and morbidity rates. Larger lesions can be radically excised in one surgical procedure by using a multidisciplinary approach. Reconstruction of the skull base with vascularized myofascial flaps reduces postoperative CSF leaks. Postoperative lower cranial nerves deficits are the most dangerous complication.
颈静脉孔区肿瘤是罕见的颅底病变,存在诊断和复杂治疗问题。本研究旨在评估过去16年中接受手术治疗的一系列颈静脉孔区肿瘤患者,并分析手术技术、并发症及预后。
作者回顾性研究了1987年1月至2004年5月间接受治疗的102例颈静脉孔区肿瘤患者。所有患者均采用神经外科与耳鼻喉技术相结合的多学科方法进行手术。对副神经节瘤和其他血供丰富的病变进行术前栓塞。为避免术后脑脊液漏并改善美容效果,用特制的带血管蒂皮瓣(颞肌筋膜、颈筋膜、胸锁乳突肌和颞肌)修复手术缺损。两名肿瘤侵犯颈内动脉的患者采用大隐静脉移植搭桥术。采用耳大神经移植或第12/7颅神经吻合术进行面神经重建。部分切除后对残留的恶性和浸润性肿瘤进行放疗。最常见的肿瘤是副神经节瘤(58例),其次是神经鞘瘤(17例)和脑膜瘤(10例)。45例副神经节瘤患者(77.5%)和所有神经鞘瘤患者均可行完整切除。最常见且最危险的手术并发症是下组颅神经功能障碍。10例患者(10%)出现此功能障碍,但4例为短暂性。8例患者(8%)术后出现面神经和耳蜗神经麻痹;其中3例自行恢复。其余5例患者中,3例采用耳大神经移植重建面神经,1例采用腓肠神经移植,1例采用舌下神经/面神经吻合术。4例患者(4%)术后出现脑脊液漏,4例(4.2%)术后死亡。其中2例死于吸入性肺炎合并败血症。其余2例中,1例死于肺栓塞,另1例死于因巨大颈部血肿导致气管移位引起的脑缺氧。
副神经节瘤是颈静脉孔区最常见的肿瘤。颈静脉孔区肿瘤的手术治疗复杂且困难。根治性切除良性颈静脉孔区肿瘤是首选治疗方法,可能治愈,且死亡率和发病率较低。采用多学科方法,较大的病变可在一次手术中根治性切除。用带血管蒂肌筋膜瓣重建颅底可减少术后脑脊液漏。术后下组颅神经功能障碍是最危险的并发症。