与套细胞淋巴瘤诱发的血管闭塞有关的缺血性视网膜病变

IF 0.5 Q4 OPHTHALMOLOGY Journal of VitreoRetinal Diseases Pub Date : 2024-11-13 DOI:10.1177/24741264241297945
Christopher A Turski, Gunay Uludag Kirimli, Lejla Vajzovic, Stephen Scott, Majda Hadziahmetovic
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引用次数: 0

摘要

目的:描述一名双侧缺血性视网膜病变患者的情况,其病因可能是套细胞淋巴瘤诱发的血管闭塞。方法:对一个病例及其研究结果进行分析:对一个病例及其研究结果进行分析。结果:一名 54 岁的男子在 11 个月前出现双眼视力明显下降。他的病史中有明显的套细胞淋巴瘤,磁共振成像没有发现眶内受累的迹象。就诊时,外侧视力为 20/400,外侧为数指,眼前节检查无异常。眼底镜检查可见视神经苍白、血管硬化和棉絮斑。荧光素血管造影和光学相干断层扫描证实了严重的视网膜非灌注和视网膜内层缺失,但发病时没有黄斑水肿的迹象。结论:本报告是首例双侧缺血性视网膜病变,很可能源自套细胞淋巴瘤,主要表现为缺血性视网膜特征,并导致视力严重下降。由于很少有病例记录套细胞淋巴瘤累及视网膜,本报告让人们更好地了解了这种罕见病变及其对视网膜健康的影响。
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Ischemic Retinopathy Associated With Mantle Cell Lymphoma-Induced Vascular Occlusion.

Purpose: To describe a patient with bilateral ischemic retinopathy, likely attributable to vascular occlusion induced by mantle cell lymphoma. Methods: A case and its findings were analyzed. Results: A 54-year-old man presented with an 11-month history of significant vision loss in both eyes. His medical history was significant for mantle cell lymphoma with no signs of intraorbital involvement on magnetic resonance imaging. At presentation, the visual acuity was 20/400 OD and counting fingers OS, with an unremarkable anterior segment examination. On fundoscopy, optic nerve pallor, sclerotic blood vessels, and cotton-wool spots were seen. Profound retinal nonperfusion and inner retinal layer loss were confirmed with fluorescein angiography and optical coherence tomography, with no signs of macular edema at the time of presentation. Conclusions: This report represents the first instance of bilateral ischemic retinopathy, likely originating from mantle cell lymphoma, presenting predominantly with ischemic retinal features and resulting in profound vision loss. With few cases documenting retinal involvement in mantle cell lymphoma, this report provides a better understanding of this rare pathology and its effect on retinal health.

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CiteScore
1.20
自引率
16.70%
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