Suri Ashish, Ahmad Faiz U, Mahapatra Ashok K
Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.
Neurosurgery. 2007 Mar;60(3):483-8; discussion 488-9. doi: 10.1227/01.NEU.0000255333.95532.13.
Cavernous sinus hemangiomas (CSHs) are uncommon lesions and comprise fewer than 1% of all parasellar masses. Because of their location, propensity for profuse bleeding during surgery, and relationship to complex neurovascular structures, they are notoriously difficult to excise.
The authors describe their experience with seven cases of CSHs. Headache and visual impairment were the most common presenting complaints, followed by facial hypesthesia and diplopia. Computed tomographic scans revealed iso- to hyperdense expansile lesions in the region of the cavernous sinus and middle cranial fossa. Magnetic resonance imaging scans revealed hypo- to isointense lesions on T1-weighted images and markedly hyperintense lesions on T2-weighted images, with marked homogeneous enhancement after contrast administration.
All CSHs were treated by a purely extradural transcavernous approach. This involved reduction of sphenoid ridge, exposure of the superior orbital fissure, drilling of the anterior clinoid process, coagulation and division of the middle meningeal artery, and peeling of the meningeal layer of the lateral wall of the cavernous sinus from the inner membranous layer. The cranial nerves in the lateral wall of the cavernous sinus were exposed (Cranial Nerves III and IV, as well as V1, V2, and V3). The tumor was accessed through its maximum bulge through either the lateral or anterolateral triangle. The tumor was removed via rapid decompression, coagulation of the feeder from the meningohypophyseal trunk, and dissection along the cranial nerves. All but one patient had complete tumor excision. Transient ophthalmoparesis (complete resolution in 6-8 wk) was the most common surgical complication.
To our knowledge, we describe one of the largest series of pure extradural transcavernous approaches to CSHs. CSHs are uncommon but challenging cranial base lesions. The extradural transcavernous approach allows complete excision with minimal mortality or long-term morbidity.
海绵窦血管瘤(CSHs)是罕见病变,占所有鞍旁肿块的比例不到1%。因其位置特殊、手术中容易大量出血以及与复杂神经血管结构的关系,其切除难度极大。
作者描述了7例海绵窦血管瘤的治疗经验。头痛和视力障碍是最常见的主诉,其次是面部感觉减退和复视。计算机断层扫描显示海绵窦区和中颅窝区域有等密度至高密度的膨胀性病变。磁共振成像扫描显示,在T1加权图像上为低信号至等信号病变,在T2加权图像上为明显高信号病变,增强扫描后有明显均匀强化。
所有海绵窦血管瘤均采用单纯硬膜外经海绵窦入路治疗。该方法包括磨除蝶骨嵴、暴露眶上裂、磨除前床突、凝固并切断脑膜中动脉,以及从内侧膜层剥离海绵窦外侧壁的脑膜层。暴露海绵窦外侧壁的脑神经(动眼神经、滑车神经以及眼神经、上颌神经和下颌神经)。通过外侧或前外侧三角的最大隆起处进入肿瘤。通过快速减压、凝固来自脑膜垂体干供血动脉以及沿脑神经进行分离来切除肿瘤。除1例患者外,其余患者肿瘤均完全切除。短暂性眼球运动麻痹(6 - 8周内完全恢复)是最常见的手术并发症。
据我们所知,我们描述了最大系列之一的单纯硬膜外经海绵窦入路治疗海绵窦血管瘤的病例。海绵窦血管瘤虽不常见,但却是具有挑战性的颅底病变。硬膜外经海绵窦入路可实现肿瘤的完全切除,且死亡率和长期发病率极低。