Rectus Muscle Metastasis from Primary Uveal Melanoma: A Case Series and Literature Review.

IF 1.2 Q4 OPHTHALMOLOGY
Ocular Oncology and Pathology Pub Date : 2026-06-01 Epub Date: 2026-01-22 DOI:10.1159/000550593
Saloni Kapoor, Asad Javed, Nasreen A Syed, Erin M Shriver, Julius I Yevdash, Colin Kenny, Jennifer Menke, H Culver Boldt, Elaine Binkley
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引用次数: 0

Abstract

Introduction: We aim to describe 2 patients with metastatic uveal melanoma who developed metastases to the contralateral rectus muscles and review the literature on this rare presentation.

Case presentations: Patient 1 was a woman in her 60s with a history of cirrhosis who presented with a medium-sized choroidal melanoma in the right eye that was treated with plaque brachytherapy. She underwent regular hepatic imaging for surveillance post-treatment. Two-and-a-half years later, she developed diplopia, and a left medial rectus muscle lesion was found on MRI imaging. Biopsy was consistent with metastatic uveal melanoma. Systemic therapy with tebentafusp was initiated. The lesion slowly progressed over 2 years. The patient passed away from complications from her cirrhosis. Patient 2 was a man in his 70s with a large choroidal melanoma in the left eye treated with enucleation. He had metastatic disease at the time of diagnosis that was treated with multiple systemic therapies. Metastases to the right superior and lateral rectus muscles were noted on MRI imaging and were initially observed. He developed painful proptosis and was found to have acute enlargement of the lesions. Treatment with 30 Gy external beam radiation to the right orbit was performed with good local response. He passed away from tumor progression.

Conclusion: Metastasis to rectus muscles from uveal melanoma has historically been exceedingly rare. These cases highlight new challenges in treating symptomatic intraorbital metastasis as surgical outcomes and survival improve in patients due to advances in systemic therapy.

原发性葡萄膜黑色素瘤的直肌转移:一个病例系列和文献回顾。
简介:我们的目的是描述2例转移性葡萄膜黑色素瘤患者,他们转移到对侧直肌,并回顾有关这种罕见表现的文献。病例介绍:患者1是一名60多岁的女性,有肝硬化病史,右眼出现中等大小的脉络膜黑色素瘤,接受了斑块近距离放疗。治疗后定期行肝显像监测。两年半后,患者出现复视,MRI检查发现左内直肌病变。活检符合转移性葡萄膜黑色素瘤。开始用替本他福进行全身治疗。病变在2年内缓慢进展。病人死于肝硬化并发症。患者2是一名70多岁的男性,左眼有一个大的脉络膜黑色素瘤,接受了去核治疗。他在诊断时患有转移性疾病,并接受了多种全身治疗。转移到右侧上直肌和外侧直肌在MRI成像上被注意到,并最初观察到。他出现了疼痛的突出,并发现病变急性扩大。采用30 Gy外束放射治疗右眼,局部反应良好。他因肿瘤恶化而去世。结论:葡萄膜黑色素瘤向直肌转移在历史上极为罕见。这些病例强调了治疗症状性眼眶内转移的新挑战,因为全身治疗的进展改善了手术结果和患者的生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
20
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