Jallo George I, Benjamin Vallo
Division of Pediatric Neurosurgery, Institute for Neurology and Neurosurgery, Beth Israel Medical Center, New York, New York 10016, USA.
Neurosurgery. 2002 Dec;51(6):1432-39; discussion 1439-40.
Despite Cushing's accurate description of the anatomic origin of tuberculum sellae meningiomas, many subsequent authors have included tumors originating from the neighboring sella region in this classification. This has led to difficulty in evaluating the surgical results and consensus for an optimal surgical technique. We think this confusion has arisen from Cushing's description of these tumors under the heading "suprasellar meningiomas," which referred to their distinctive clinical symptoms and not their anatomic origin. We describe the microsurgical anatomy and tumor growth patterns to reemphasize the original classification of Cushing's tuberculum sellae meningiomas. Additionally, we describe our surgical approach, which decreases the risk of injury to anterior visual pathways and anterior cerebral circulation arteries.
During a 19-year period, 23 patients with meningiomas arising from the tuberculum and diaphragma sellae underwent craniotomies at New York University Medical Center. The tumor size ranged from 2 to 5 cm. All patients presented with symptoms of visual dysfunction; 15 were asymmetrical. Magnetic resonance imaging with and without gadolinium differentiated these tumors from other suprasellar tumors with a high degree of accuracy. All patients underwent a pterional transsylvian approach.
Twenty patients had total tumor removal, and three had subtotal tumor removal. There was one regrowth in the subtotal tumor removal group. Patients were observed for a mean follow-up time of 9.3 years (range, 3.6-18.5 yr). Visual acuity improved in 55%, was unchanged in 26%, and worsened in 19% of patients. Two of the oldest patients died from pulmonary complications, resulting in a mortality rate of 8.7%.
We think that tuberculum and diaphragma sellae meningiomas are anatomically indistinguishable and should be termed tuberculum sellae meningioma. A pterional craniotomy with microsurgical dissection of the sylvian fissure allows access to these tumors with minimal neurological and ophthalmological morbidity.
尽管库欣对鞍结节脑膜瘤的解剖起源描述准确,但许多后续作者在该分类中纳入了起源于相邻鞍区的肿瘤。这导致在评估手术结果和确定最佳手术技术的共识方面存在困难。我们认为这种混淆源于库欣在“鞍上脑膜瘤”标题下对这些肿瘤的描述,该描述指的是它们独特的临床症状而非解剖起源。我们描述显微手术解剖结构和肿瘤生长模式,以再次强调库欣鞍结节脑膜瘤的原始分类。此外,我们描述我们的手术方法,该方法可降低对视神经前通路和大脑前循环动脉损伤的风险。
在19年期间,23例起源于鞍结节和鞍隔的脑膜瘤患者在纽约大学医学中心接受了开颅手术。肿瘤大小为2至5厘米。所有患者均出现视觉功能障碍症状;15例不对称。增强和未增强的磁共振成像能高度准确地将这些肿瘤与其他鞍上肿瘤区分开来。所有患者均采用翼点经侧裂入路。
20例患者肿瘤全切,3例次全切除。次全切除组有1例复发。患者平均随访时间为9.3年(范围3.6 - 18.5年)。55%的患者视力改善,26%不变,19%恶化。2例年龄最大的患者死于肺部并发症,死亡率为8.7%。
我们认为鞍结节和鞍隔脑膜瘤在解剖学上无法区分,应称为鞍结节脑膜瘤。采用翼点开颅并对侧裂进行显微解剖,可在对神经和眼科发病率最小的情况下接近这些肿瘤。