Chernov S V, Rzaev D A, Kalinovsky A V, Dmitriev A B, Kasymov A R, Zotov A V, Gormolysova E V, Uzhakova E K
Federal Neurosurgical Center, Nemirovicha-Danchenko Str., 132/1, Novosibirsk, 630087, Russia.
Zh Vopr Neirokhir Im N N Burdenko. 2017;81(1):74-80. doi: 10.17116/neiro201780774-80.
Resection of anterior clinoidal meningiomas is a challenging task due to their localization, frequent involvement of the major cerebral arteries and cranial nerves, a high risk of postoperative neurological deficits, and low radicalness of surgery.
To evaluate the radicalness of microsurgical removal and a neurological deficit in the early postoperative period in patients with anterior clinoidal meningiomas.
A total of 35 patients with anterior clinoidal meningiomas underwent surgery at the Department of Neurooncology of the Novosibirsk Federal Neurosurgical Center in the period from 2013 to July 2016. There were 29 (82.9%) females and 6 (17.1%) males. The mean patient age was 50.1 years (31-72 years). According to the Al-Mefty classification (1990), type 1 tumors occurred in 10 (28.6%) patients, type 2 tumors were in 22 (62.8%) patients, and type 3 tumors were in 3 (8.6%) patients. Twenty four (68.6%) patients had large (greater than 4.0 cm) tumors, 7 (20.0%) patients had medium (2.0-4.0 cm) tumors, and 4 (11.4%) patients had small (less than 2.0 cm) meningiomas. The tumor involved the major arteries in 21 (60.0%) patients.
The lateral supraorbital approach was used in 26 (74.3%) patients, and the pterional approach was used in 9 (25.7%) cases. The tumor was resected totally (Simpson II) in 25 (71.4%) cases and subtotally (Simpson IV, subtype A and B) in 10 (28.6%) patients. In the early postoperative period, cerebral symptoms regressed in 20 (57.1%) patients; visual acuity improved in 2 of 13 (15.4%) patients. Four (11.4%) patients developed IIIrd nerve palsy; 2 (5.7%) patients developed severe hemiparesis. The mortality rate was 2.9%.
The completeness of resection directly depends on the tumor consistency: soft meningiomas can be totally resected (Simpson II) with a good functional outcome. In the case of solid tumors, total resection may lead to serious ischemic disorders with a high risk of death.
前床突脑膜瘤的切除是一项具有挑战性的任务,因其位置特殊,常累及大脑主要动脉和颅神经,术后神经功能缺损风险高,且手术根治性低。
评估前床突脑膜瘤患者显微手术切除的根治性及术后早期的神经功能缺损情况。
2013年至2016年7月期间,共有35例前床突脑膜瘤患者在新西伯利亚联邦神经外科中心神经肿瘤学部门接受手术。其中女性29例(82.9%),男性6例(17.1%)。患者平均年龄为50.1岁(31 - 72岁)。根据Al - Mefty分类(1990年),1型肿瘤患者10例(28.6%),2型肿瘤患者22例(62.8%),3型肿瘤患者3例(8.6%)。24例(68.6%)患者肿瘤较大(直径大于4.0 cm),7例(20.0%)患者肿瘤中等大小(2.0 - 4.0 cm),4例(11.4%)患者肿瘤较小(直径小于2.0 cm)。21例(60.0%)患者的肿瘤累及主要动脉。
26例(74.3%)患者采用眶上外侧入路,9例(25.7%)患者采用翼点入路。25例(71.4%)患者肿瘤全切(Simpson II级),10例(28.6%)患者肿瘤次全切除(Simpson IV级,A和B亚型)。术后早期,20例(57.1%)患者的脑部症状消退;13例患者中有2例(15.4%)视力改善。4例(11.4%)患者出现动眼神经麻痹;2例(5.7%)患者出现严重偏瘫。死亡率为2.9%。
切除的完整性直接取决于肿瘤质地:质地柔软的脑膜瘤可全切(Simpson II级),功能预后良好。对于质地坚实的肿瘤,全切可能导致严重的缺血性病变,死亡风险高。