Corazzelli Giuseppe, Russo Federico, Corvino Sergio, Germano Cristiana, Dello Iacovo Filippo, Cioffi Valentina, Di Colandrea Salvatore, Bonavolontà Paola, De Divitiis Oreste, De Falco Raffaele, Bocchetti Antonio
Department of Neurosciences and Reproductive and Odontostomatological Sciences, Neurosurgical Clinic, University of Naples Federico II, Naples, ITA.
Department of Public Health, Division of Pathological Anatomy, University of Naples Federico II, Naples, ITA.
Cureus. 2024 Nov 5;16(11):e73033. doi: 10.7759/cureus.73033. eCollection 2024 Nov.
Head and neck squamous cell carcinoma (HNSCC) can, in rare instances, metastasize to the CNS, which is often associated with a poor prognosis. We present the case of a 65-year-old male with a history of HNSCC who developed two enhancing brain lesions: one in the right parietal region and another in the right insular region. Initially, the patient was managed with CyberKnife radiosurgery targeting both lesions. However, he later experienced neurological symptoms, including confusion, gait instability, and a left Jacksonian march, primarily attributed to the progression of the right parietal lesion. Given this symptomatic presentation, surgical resection of the lesion was performed to confirm the diagnosis and provide symptomatic relief. The surgical approach was selected based on the patient's clinical progression and imaging findings, with the goal of improving his quality of life. Despite surgical intervention, the patient's condition deteriorated, and he passed away seven months later. This case illustrates the complexity of treating CNS metastases from HNSCC, highlighting the challenges in surgical decision-making and the role of adjuvant therapies. The rarity of CNS metastases in HNSCC adds to the difficulty of management, underscoring the importance of a multidisciplinary approach. Further investigation is needed to develop standardized treatment protocols for such rare presentations. CNS metastases in HNSCC are uncommon and typically indicate a poor outcome. This case reinforces the need for ongoing research to enhance management strategies and improve patient survival in similar cases.
头颈部鳞状细胞癌(HNSCC)在极少数情况下可转移至中枢神经系统(CNS),这通常与预后不良相关。我们报告一例65岁男性HNSCC患者,其脑部出现两个强化病灶:一个位于右侧顶叶区域,另一个位于右侧岛叶区域。最初,患者接受了针对这两个病灶的射波刀放射外科治疗。然而,他后来出现了神经症状,包括意识模糊、步态不稳和左侧杰克逊癫痫发作,主要归因于右侧顶叶病灶的进展。鉴于这种症状表现,对该病灶进行了手术切除以明确诊断并缓解症状。手术方式根据患者的临床进展和影像学检查结果选择,目的是改善其生活质量。尽管进行了手术干预,但患者病情仍恶化,七个月后去世。该病例说明了治疗HNSCC脑转移瘤的复杂性,凸显了手术决策的挑战以及辅助治疗的作用。HNSCC脑转移瘤的罕见性增加了治疗难度,强调了多学科方法的重要性。需要进一步研究以制定针对此类罕见病例的标准化治疗方案。HNSCC脑转移瘤并不常见,通常提示预后不良。该病例强化了持续开展研究以加强管理策略并改善类似病例患者生存率的必要性。