Department of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, Florida, USA.
Department of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, Florida, USA.
World Neurosurg. 2021 Apr;148:205. doi: 10.1016/j.wneu.2021.01.069. Epub 2021 Jan 28.
Meningiomas of the cavernous sinus (CS) present a neurosurgical challenge. The anatomic complexity of the area can create a potential for injury to neurovascular structures. This has traditionally limited total tumor removal. A thorough understanding of the cavernous sinus surgical anatomy can help overcome this problem. Patients with CS meningiomas generally present with cranial nerve deficits (III-VI), proptosis, and visual disturbances. Management of CS tumors is controversial and includes observation, stereotactic radiosurgery, and surgical resection. We present the case of a 43-year-old right-handed male who presented with right facial numbness. A magnetic resonance imaging scan of the brain showed a right cavernous sinus tumor. He underwent stereotactic radiosurgery at an outside hospital. His facial numbness gradually improved. Four years later he had recurrence of the right facial numbness in the V3 distribution associated with right eyelid ptosis and diplopia. On neurologic examination he had decreased sensation to light touch in the 3 branches of the trigeminal nerve. He had a right eyelid ptosis and a 6-VI cranial nerve palsy. A new magnetic resonance imaging scan of the brain showed radiologic progression of the tumor. An orbitozygomatic craniotomy was performed and gross total tumor resection was achieved through lateral wall of the cavernous sinus working mainly between V2 and V3. The facial numbness he had preoperatively gradually improved, and his extraocular movements and eyelid ptosis recovered completely. Histopathology showed a clear cell grade 2 meningioma. The patient received adjuvant radiosurgery. At 3-year follow-up, the patient was free of disease recurrence. CS surgery for meningioma is feasible with low morbidity and can provide benefits in improving preexisting cranial nerve dysfunction (Video 1). Complete resection of the CS meningiomas is possible in most cases. CS tumors remain a surgical challenge, but accurate knowledge of surgical neuroanatomy and surgical approaches facilitates their safe and effective treatment. The patient gave informed consent for surgery, use of images, and video publication.
海绵窦脑膜瘤(CS)是神经外科的一个挑战。该区域的解剖复杂性可能导致对神经血管结构造成损伤。这传统上限制了肿瘤的完全切除。对海绵窦手术解剖的透彻理解可以帮助克服这个问题。CS 脑膜瘤患者通常表现为颅神经缺损(III-VI)、眼球突出和视力障碍。CS 肿瘤的治疗方法存在争议,包括观察、立体定向放射外科和手术切除。我们报告了一名 43 岁的右利手男性患者,他因右侧面部麻木就诊。颅脑磁共振成像扫描显示右侧海绵窦肿瘤。他在一家外院接受了立体定向放射外科治疗。他的面部麻木逐渐改善。四年后,他出现右侧 V3 分布的面部麻木复发,伴有右侧上睑下垂和复视。神经检查发现他的三叉神经三支的轻触觉感觉减退。他有右侧上睑下垂和 VI 颅神经麻痹。颅脑新磁共振成像扫描显示肿瘤的影像学进展。行眶颧开颅术,通过海绵窦外侧壁行大体全切除,主要在 V2 和 V3 之间操作。术前他的面部麻木逐渐改善,眼外肌运动和上睑下垂完全恢复。组织病理学显示为透明细胞 II 级脑膜瘤。患者接受了辅助放射外科治疗。在 3 年的随访中,患者无疾病复发。CS 脑膜瘤手术可行,发病率低,可以改善现有颅神经功能障碍(视频 1)。大多数情况下,CS 脑膜瘤可以实现完全切除。CS 肿瘤仍然是一个手术挑战,但对手术神经解剖和手术入路的准确了解可以促进其安全有效的治疗。患者对手术、图像使用和视频发表知情同意。