Miyagi A, Maeda K, Sugawara T
Department of Neurosurgery, Higashijyujyo Hospital, Tokyo, Japan.
No Shinkei Geka. 1998 Feb;26(2):169-75.
We report a case of large clival chordoma. The patient was a 56-year-old male who was admitted to our hospital with left eye ptosis and diplopia of 2 months duration. On admission, neurological examinations revealed oculomotor nerve palsy of the left eye. Skull radiographs with polytomographs demonstrated marked destruction of the clivus. A plain computed tomography (CT) scan revealed a large iso-attenuated mass in the clivus, extending anteriorly into the sphenoidal sinus, superiorly into the suprasellar cistern, bilaterally into the petrous apex, posteriorly into the prepontine cistern and caudally into the foramen magnum. An enhanced CT scan demonstrated a slightly enhanced tumor. A high-resolution bone-window CT scan revealed marked destruction of the clivus and bilateral petrous apex. Magnetic resonance imaging (MRI) scans disclosed a large enhanced mass extending superiorly into the suprasellar cistern, bilaterally into the petrous apex and inferiorly into the foramen magnum. The tumor extended so widely that we decided on a one-stage operation via a transsphenoidal sublabial transseptal approach and transoral transpalatal approach. At surgery, we employed a neuronavigator and Codman 4-mm rigid neuroendoscope with 0 degree, 30 degrees and 70 degrees angled lenses. The tumor was very soft and suckable, and could be easily removed by applying CUSA, a pituitary curette and suction. The neuronavigator was particularly useful because the surgeon had a real-time two-dimensional representation of the position of the tip of this device in the corresponding imaging space intraoperatively. The neuroendoscope also proved useful, since remnant tumor tissues that could not be seen under an operating microscope were frequently recognized near or around the entrance of the tumor cavity, cavernous sinus region and petroclival junction area. The surgeon was able to remove these remnants safely by checking on the neuroendoscope monitor. The tumor was excised completely. The dead space of the tumor cavity was reconstructed using a free rectus abdominis muscle flap. Postoperatively, cerebrospinal fluid leakage and meningitis were recognized, but improved following spinal drainage for one week and intrathecal injection of antibiotic. The oculomotor nerve palsy of the left eye also showed good recovery at one month after the operation. Recently, skull base surgery has undergone considerable developments. Neuroendoscopes and neuronavigators are very helpful for the neurosurgeon in performing skull base tumor surgery safely and with precision, although further instrument modifications are needed.
我们报告一例巨大斜坡脊索瘤病例。患者为一名56岁男性,因左眼上睑下垂和复视2个月入院。入院时,神经系统检查发现左眼动眼神经麻痹。头颅X线断层摄影显示斜坡明显破坏。普通计算机断层扫描(CT)显示斜坡有一巨大等密度肿块,向前延伸至蝶窦,向上延伸至鞍上池,双侧延伸至岩尖,向后延伸至脑桥前池,向下延伸至枕骨大孔。增强CT扫描显示肿瘤轻度强化。高分辨率骨窗CT扫描显示斜坡和双侧岩尖明显破坏。磁共振成像(MRI)扫描显示一巨大强化肿块,向上延伸至鞍上池,双侧延伸至岩尖,向下延伸至枕骨大孔。肿瘤广泛蔓延,因此我们决定通过经蝶窦唇下经鼻中隔入路和经口经腭入路进行一期手术。手术中,我们使用了神经导航仪和Codman 4毫米刚性神经内镜,配有0度、30度和70度角的镜头。肿瘤非常柔软,可吸出,使用超声吸引器、垂体刮匙和吸引器可轻松切除。神经导航仪特别有用,因为术中外科医生能在相应成像空间中实时获得该设备尖端位置的二维图像。神经内镜也证明很有用,因为在手术显微镜下看不到的残留肿瘤组织常在肿瘤腔入口附近、海绵窦区域和岩斜交界区被发现。外科医生通过查看神经内镜监视器能够安全地清除这些残留组织。肿瘤被完全切除。肿瘤腔的死腔用游离腹直肌瓣重建。术后,出现了脑脊液漏和脑膜炎,但经一周的脊髓引流和鞘内注射抗生素后情况好转。术后1个月,左眼动眼神经麻痹也显示出良好的恢复。近来,颅底手术有了很大进展。神经内镜和神经导航仪对神经外科医生安全、精确地进行颅底肿瘤手术非常有帮助,不过还需要对器械做进一步改进。