Rico Pereira Marta, Muñoz Hernández Fernando
Department of Neurosurgery, Hospital Sant Pau, Barcelona, Spain.
Institut d'Investigació Biomèdica Sant Pau, Sant Quintí, Barcelona, Spain.
Asian J Neurosurg. 2025 Mar 24;20(2):423-426. doi: 10.1055/s-0045-1806729. eCollection 2025 Jun.
Anterior clinoid process metastases are rare. We present an unusual case of anterior clinoid process metastasis with sudden deterioration of visual function requiring emergency optic nerve decompression, resulting in recovery of visual function. The patient was a 41-year-old man with a diagnosis of leiomyosarcoma of the radius, operated on in 2014, with bone and lung metastases, who had been treated with chemotherapy and appeared to have stable disease at his last follow-up. Six years later, he developed a 1-month history of progressive unilateral loss of visual acuity and visual field defect (initially quadrantanopia that progressed to nasal hemianopia). Brain imaging showed a contrast-enhancing lesion affecting the left anterior clinoid process with extension to the cavernous sinus and sphenoid sinus, causing compression of the left optic nerve. Although the lesion could have suggested a meningioma given the location, in the context of the patient's oncological history, the diagnosis of metastasis was considered more likely. The patient was admitted to the hospital and, during the hospital stay, developed sudden left retro-orbital pain progressing to left amaurosis over approximately 8 hours. Urgent surgery was performed: a pterional craniotomy with partial tumor removal and optic nerve decompression with extradural anterior clinoidectomy. After surgery, the patient had an immediate but partial improvement in visual acuity and in the visual field defect. Metastasis to the anterior clinoid process is very uncommon, with only one case previously reported in the literature. In cases of visual impairment, symptoms may deteriorate rapidly to complete loss of vision, so urgent decompressive surgery of the optic pathway may be indicated to recover visual function, although recovery may be partial.
前床突转移瘤较为罕见。我们报告了一例不寻常的前床突转移瘤病例,患者视觉功能突然恶化,需要紧急进行视神经减压,术后视觉功能得以恢复。该患者为一名41岁男性,2014年诊断为桡骨平滑肌肉瘤,已发生骨和肺转移,接受过化疗,上次随访时病情似乎稳定。六年后,他出现了1个月的渐进性单侧视力丧失和视野缺损病史(最初为象限盲,逐渐发展为鼻侧偏盲)。脑部影像学检查显示,一个强化病灶累及左侧前床突,并延伸至海绵窦和蝶窦,压迫左侧视神经。尽管鉴于病灶位置可能提示为脑膜瘤,但结合患者的肿瘤病史,转移瘤的诊断更有可能。患者入院后,住院期间突然出现左侧眶后疼痛,并在约8小时内发展为左侧黑矇。遂紧急进行手术:经翼点开颅,部分切除肿瘤,并通过硬膜外前床突切除术进行视神经减压。术后,患者视力和视野缺损立即得到部分改善。前床突转移非常罕见,文献中此前仅报道过一例。在出现视力损害的病例中,症状可能迅速恶化至完全失明,因此尽管恢复可能不完全,但可能仍需紧急对视神经通路进行减压手术以恢复视觉功能。