Bilateral Blindness Due to Radiation-Induced Optic Neuropathy in a Patient with Nasal Mucosal Melanoma.

Mauricio Agustin Benetti, Luciana León-Cejas, Luis Ariel Miquelini, Dolores Ribero-Ayerza, Francisco Caiza-Zambrano, Ricardo Reisin
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Abstract

Radiation-induced optic neuropathy is an uncommon but devastating complication of radiotherapy for head and neck tumors, characterized by subacute, painless, irreversible visual loss. Nasal mucosal melanoma, although rare, carries a high risk of visual pathway toxicity due to its proximity to anterior optic structures. We report the case of a 73-year-old woman with right nasal mucosal melanoma treated with adjuvant radiotherapy (66 Gy) and anti-PD1 immunotherapy, who developed progressive bilateral vision loss. Neuro-ophthalmological examination revealed severe visual acuity reduction, bilateral mydriasis, and optic disc pallor. Optical coherence tomography showed retinal nerve fiber layer thinning. Brain MRI demonstrated contrast enhancement of the optic chiasm and prechiasmatic optic nerves. Despite intensive treatment, the patient progressed to bilateral blindness. This case underscores the importance of early recognition of radiation-induced optic neuropathy, particularly in high-risk anatomical sites and in patients receiving radiotherapy combined with immunotherapy.

鼻黏膜黑色素瘤患者放射性视神经病变致双侧失明1例。
放射性视神经病变是头颈部肿瘤放射治疗中一种罕见但具有破坏性的并发症,其特点是亚急性、无痛、不可逆的视力丧失。鼻黏膜黑色素瘤虽然罕见,但由于其靠近前视结构,因此具有很高的视觉通路毒性风险。我们报告一例73岁女性右鼻黏膜黑色素瘤患者,接受辅助放疗(66 Gy)和抗pd1免疫治疗,并发进行性双侧视力丧失。神经眼科检查显示严重的视力下降,双侧瞳孔肿大,视盘苍白。光学相干断层扫描显示视网膜神经纤维层变薄。脑MRI显示视交叉和交叉前视神经增强。尽管进行了强化治疗,患者仍发展为双侧失明。该病例强调了早期识别辐射引起的视神经病变的重要性,特别是在高危解剖部位和接受放疗联合免疫治疗的患者中。
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