Systemic Hodgkin Lymphoma with Presumed Intraocular Involvement

Victoria A. Marks, Vijitha S. Vempuluru, Carol L. Shields
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Abstract

We report a rare case of systemic Hodgkin lymphoma with presumed intraocular involvement that resolved following systemic chemotherapy. Observational case report. A 32-year-old woman with known stage II Hodgkin lymphoma presented with 3 months of photopsia and decreased vision in the left eye. Fundus examination demonstrated vitreous cells, more than 100 yellow choroidal infiltrates involving the entire fundus, and retinal pigment epithelial defects in the macular region of the left eye. Ultrasonography showed chorioretinal thickening and optical coherence tomography demonstrated vitreous opacities with outer retinal atrophy, irregular retinal pigment epithelial thickening, and hyper-transmission defects. A diagnosis of Hodgkin lymphoma with vitreoretinal involvement was considered. Fine needle aspiration biopsy was considered, but the patient preferred deferral as she was already on cycle 3 of systemic chemotherapy (doxorubicin, bleomycin, vinblastine, dacarbazine). Following the fourth cycle of systemic treatment, the vitreous cells and choroidal lesions resolved. This case details a rare presentation of systemic Hodgkin lymphoma with presumed vitreoretinal and choroidal involvement that responded to anti-Hodgkin lymphoma chemotherapy.
推测眼内受累的系统性霍奇金淋巴瘤
我们报告了一例罕见的全身性霍奇金淋巴瘤眼内受累病例。 观察性病例报告。 一名 32 岁的女性患者患有已知的霍奇金淋巴瘤 II 期,发病 3 个月来左眼出现畏光和视力下降。眼底检查显示左眼玻璃体细胞、100 多个黄色脉络膜浸润累及整个眼底,黄斑区视网膜色素上皮缺损。超声波检查显示脉络膜视网膜增厚,光学相干断层扫描显示玻璃体混浊,视网膜外层萎缩,视网膜色素上皮不规则增厚,以及过度透射缺陷。考虑诊断为玻璃体视网膜受累的霍奇金淋巴瘤。曾考虑进行细针穿刺活检,但由于患者已经接受了第 3 个周期的全身化疗(多柔比星、博来霉素、长春新碱、达卡巴嗪),因此她倾向于推迟。在接受了第四个周期的全身治疗后,玻璃体细胞和脉络膜病变得到了缓解。 本病例详细描述了一个罕见的全身性霍奇金淋巴瘤病例,患者推测玻璃体视网膜和脉络膜受累,并对抗击霍奇金淋巴瘤化疗产生了反应。
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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