Elshamy Walid, Soylemez Burcak, Sayyahmelli Sima, Keser Nese, Baskaya Mustafa K
Department of Neurological Surgery, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, United States.
Department of Neurological Surgery, Ain Shams University, Faculty of Medicine, Cairo, Egypt.
J Neurol Surg B Skull Base. 2021 May 11;83(Suppl 3):e644-e645. doi: 10.1055/s-0041-1727124. eCollection 2022 Aug.
Chondrosarcomas are one of the major malignant neoplasms which occur at the skull base. These tumors are locally invasive. Gross total resection of chondrosarcomas is associated with longer progression-free survival rates. The patient is a 55-year-old man with a history of dysphagia, left eye dryness, hearing loss, and left-sided facial pain. Magnetic resonance imaging (MRI) showed a giant heterogeneously enhancing left-sided skull base mass within the cavernous sinus and the petrous apex with extension into the sphenoid bone, clivus, and the cerebellopontine angle, with associated displacement of the brainstem ( Fig. 1 ). An endoscopic endonasal biopsy revealed a grade-II chondrosarcoma. The patient was then referred for surgical resection. Computed tomography (CT) scan and CT angiogram of the head and neck showed a left-sided skull base mass, partial destruction of the petrous apex, and complete or near-complete occlusion of the left internal carotid artery. Digital subtraction angiography confirmed complete occlusion of the left internal carotid artery with cortical, vertebrobasilar, and leptomeningeal collateral development. The decision was made to proceed with a left-sided transcavernous approach with possible petrous apex drilling. During surgery, minimal petrous apex drilling was necessary due to autopetrosectomy by the tumor. Endoscopy was used to assist achieving gross total resection ( Fig. 2 ). Surgery and postoperative course were uneventful. MRI confirmed gross total resection of the tumor. The histopathology was a grade-II chondrosarcoma. The patient received proton therapy and continues to do well without recurrence at 4-year follow-up. This video demonstrates steps of the combined microsurgical skull base approaches for resection of these challenging tumors. The link to the video can be found at: https://youtu.be/WlmCP_-i57s .
软骨肉瘤是发生于颅底的主要恶性肿瘤之一。这些肿瘤具有局部侵袭性。软骨肉瘤的全切除与更长的无进展生存率相关。患者为一名55岁男性,有吞咽困难、左眼干涩、听力丧失和左侧面部疼痛病史。磁共振成像(MRI)显示左侧海绵窦和岩尖内有一个巨大的、不均匀强化的颅底肿块,延伸至蝶骨、斜坡和桥小脑角,并伴有脑干移位(图1)。内镜下鼻内活检显示为二级软骨肉瘤。随后患者被转诊进行手术切除。头颈部计算机断层扫描(CT)和CT血管造影显示左侧颅底肿块、岩尖部分破坏以及左侧颈内动脉完全或近乎完全闭塞。数字减影血管造影证实左侧颈内动脉完全闭塞,伴有皮质、椎基底和软脑膜侧支循环形成。决定采用左侧经海绵窦入路并可能进行岩尖钻孔。手术过程中,由于肿瘤导致的岩尖自切除,只需进行最小程度的岩尖钻孔。使用内镜辅助实现全切除(图2)。手术及术后过程顺利。MRI证实肿瘤已全切除。组织病理学检查为二级软骨肉瘤。患者接受了质子治疗,在4年随访中无复发,情况良好。本视频展示了联合显微外科颅底入路切除这些具有挑战性肿瘤的步骤。视频链接可在:https://youtu.be/WlmCP_-i57s 找到。