Chi-Yeh Wu, Chun-Chen Chen, Shiow-Wen Liou, Ju-Chuan Yen
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引用次数: 0
摘要
本报告描述了一例独特的全身性弥漫大 B 细胞淋巴瘤(DLBCL)病例,其最初的眼部表现为双侧视盘水肿和浆液性视网膜脱离(SRD)。一名29岁的男子因左眼色觉改变、轻度发热、乏力和头痛就诊,随后出现双侧视力下降。眼前节和玻璃体检查显示没有炎症,光反射反应迟钝。他的眼底检查显示双侧多发性色素沉着,视盘肿胀,脉络膜增厚。在荧光素血管造影检查中,发现双侧有针尖状高荧光、伴有染料汇集和视盘染色渗漏。实验室检查显示,C 反应蛋白升高,白细胞轻度增多,中性粒细胞占优势。他被初步诊断为可能患有 Vogt-Koyanagi-Harada 综合征,并接受了甲基强的松龙脉冲治疗。五天后,在最初的眼部症状改善后,他的全身状况恶化。全身计算机断层扫描发现了簇状淋巴结病变,淋巴结活检后被解释为 DLBCL。DLBCL 化疗后,他的眼部症状有所改善。我们希望通过本病例和文献回顾,促进早期识别和适当检查。
Bilateral optic disc edema and serous retinal detachment as initial ocular manifestations of systemic lymphoma: A case report and literature review.
This report describes a unique case of systemic diffuse large B-cell lymphoma (DLBCL) with initial ocular manifestations of bilateral optic disc edema and serous retinal detachment (SRD). A 29-year-old man presented with altered color vision in the left eye, mild fever, weakness, and headache, followed by bilaterally reduced visual acuity. Anterior segment and vitreous examinations showed no inflammation with sluggish response of light reflex. His fundus examination revealed bilateral multiple SRDs and optic disc swelling with choroidal thickening. On fluorescein angiography, pinpoint hyperfluorescence, associated dye pooling, and optic disc staining with leakage were found bilaterally. Laboratory studies revealed elevated C-reactive protein and mild leukocytosis with neutrophil predominance. He was provisionally diagnosed with probable Vogt-Koyanagi-Harada syndrome and received methylprednisolone pulse therapy. Five days later, his systemic condition deteriorated following initial ocular symptom improvement. Whole-body computerized tomography revealed clustered lymphadenopathies, which were interpreted as DLBCL after lymph node biopsy. His ocular condition improved after DLBCL chemotherapy. We hope to promote early recognition with appropriate workups through this case and literature review.