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一名68岁男性喉鳞状细胞癌的孤立性脑转移:病例报告

Solitary brain metastasis from laryngeal squamous cell carcinoma in a 68-year-old male: A Case Report.

作者信息

Khan Allahdad, Riaz Abdul Ahad, Ahmed Shahroze, Malik Anam, Antar Mohamed, Ahmed Raheel

机构信息

Department of Medicine, Nishtar Medical University, Multan, Pakistan.

Department of Radiology, Shaukat Khanum Memorial Cancer Hospital & Research Centre, Lahore, Pakistan.

出版信息

Ann Med Surg (Lond). 2025 Jul 18;87(8):5296-5299. doi: 10.1097/MS9.0000000000003549. eCollection 2025 Aug.

Abstract

INTRODUCTION AND IMPORTANCE

Laryngeal squamous cell carcinoma (LSCC) commonly metastasizes to regional lymph nodes, lungs, liver, and bones. Intracranial metastasis from LSCC is exceedingly rare, reported in only 0.4% of cases. The atypical presentation can delay diagnosis and negatively impact prognosis. We report a rare case of solitary brain metastasis from LSCC, highlighting the diagnostic challenges and clinical considerations.

CASE PRESENTATION

A 68-year-old Pakistani male with a prior diagnosis of LSCC presented with new-onset generalized tonic-clonic seizures. He had previously undergone total laryngectomy, radiotherapy, and chemotherapy. Brain MRI revealed a right frontal lobe lesion with surrounding edema, consistent with a solitary metastasis. Histopathology following craniotomy confirmed metastatic squamous cell carcinoma. The patient was managed with antiepileptics and referred for palliative whole-brain radiotherapy. He and his family opted for palliative care, declining further aggressive treatment.

CLINICAL DISCUSSION

Distant brain metastasis in LSCC is rare and may occur without prior systemic spread. The mechanism may involve perineural invasion, although the exact pathophysiology remains unclear. Current diagnostic approaches include MRI and FDG-PET/CT. Due to limited cases, standardized treatment protocols are lacking. Management options include surgery, radiotherapy, chemotherapy, and palliative care, depending on disease progression and patient preference. Seizures as a presenting symptom are uncommon but may indicate intracranial involvement.

CONCLUSION

This case emphasizes the need for high clinical suspicion and comprehensive neurological assessment in patients with advanced LSCC. Early diagnosis and multidisciplinary management are essential for improving outcomes in this rare but serious manifestation.

摘要

引言与重要性

喉鳞状细胞癌(LSCC)通常会转移至区域淋巴结、肺、肝和骨骼。LSCC发生颅内转移极为罕见,仅在0.4%的病例中报道过。非典型表现会延迟诊断并对预后产生负面影响。我们报告一例LSCC孤立性脑转移的罕见病例,强调诊断挑战和临床考量。

病例介绍

一名68岁的巴基斯坦男性,既往诊断为LSCC,出现新发全身性强直阵挛性癫痫发作。他此前接受了全喉切除术、放疗和化疗。脑部MRI显示右侧额叶有一个伴有周围水肿的病灶,符合孤立性转移。开颅术后的组织病理学证实为转移性鳞状细胞癌。患者接受抗癫痫药物治疗,并被转诊接受姑息性全脑放疗。他和家人选择了姑息治疗,拒绝进一步积极治疗。

临床讨论

LSCC发生远处脑转移很罕见,可能在没有先前全身扩散的情况下出现。其机制可能涉及神经周围侵犯,尽管确切的病理生理学仍不清楚。目前的诊断方法包括MRI和FDG-PET/CT。由于病例有限,缺乏标准化的治疗方案。治疗选择包括手术、放疗、化疗和姑息治疗,具体取决于疾病进展和患者偏好。癫痫作为首发症状并不常见,但可能提示颅内受累。

结论

该病例强调了对晚期LSCC患者要有高度的临床怀疑和全面的神经学评估。早期诊断和多学科管理对于改善这种罕见但严重表现的预后至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8477/12333697/a726dcd9cb60/ms9-87-5296-g001.jpg

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