SYSTEMIC LYMPHOMA MASQUERADING AS BIRDSHOT CHORIORETINOPATHY.

Q3 Medicine
Elizabeth Y Wei, Marko M Popovic, Panos G Christakis
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引用次数: 0

Abstract

Purpose: To report a rare case of systemic lymphoma causing a birdshot-like chorioretinopathy in a histocompatibility leukocyte antigen-A29-negative patient.

Methods: A 58-year-old man presented with a 1-year history of blurry vision and intermittent floaters. He had evidence of bilateral choroidal birdshot-like lesions that appeared atrophic without any vitritis. He had a history of low-grade B-cell lymphoma and chronic myeloid leukemia, both of which were diagnosed >10 years before presentation and treated with chemotherapy.

Results: The differential diagnosis of these birdshot-like lesions included autoimmune, neoplastic, and infectious etiologies. Work-up revealed a negative histocompatibility leukocyte antigen-A29 and negative results for syphilis and tuberculosis. Magnetic resonance imaging revealed enhancement of the trigeminal and oculomotor nerve cisternal segments but no overt evidence of malignancy. Full-field electroretinogram and multifocal electroretinogram tests were within normal limits. Serial follow-up clinical examinations, retinal imaging, full-field electroretinogram, and multifocal electroretinogram demonstrated no disease progression. Two years after his initial consultation, he developed a paraspinal mass that was biopsied and found to be diffuse large B-cell lymphoma and was treated with chemotherapy.

Conclusion: Clinicians should consider birdshot-like chorioretinopathy masquerade syndromes in patients who present with birdshot-like choroidal lesions with negative histocompatibility leukocyte antigen-A29, a history of lymphoma, or atypical characteristics. In this case, the authors suspect the patient's past low-grade B-cell lymphoma, and chemotherapy resulted in the chronic choroidal findings. It is unclear whether choroidal involvement predisposes a patient to high-grade transformation to diffuse large B-cell lymphoma. His ocular findings remained inactive throughout the treatment of his diffuse large B-cell lymphoma.

伪装成鸟射型脉络膜视网膜病变的全身性淋巴瘤。
目的:报告一例组织相容性白细胞抗原(HLA)-A29 阴性的全身淋巴瘤引起鸟枪样脉络膜视网膜病变(BSCR)的罕见病例:一名 58 岁的男子因视力模糊和间歇性浮游物就诊一年。双侧脉络膜鸟枪样病变,呈萎缩性,无玻璃体炎。他曾患低度B细胞淋巴瘤和慢性髓性白血病,这两种疾病均在发病前10年以上确诊,并接受了化疗:这些鸟枪样病变的鉴别诊断包括自身免疫、肿瘤和感染病因。检查结果显示,HLA-A29阴性,梅毒和结核阴性。磁共振成像(MRI)显示三叉神经和眼球运动神经睫状体节段增强,但没有明显的恶性证据。全场视网膜电图(ffERG)和多灶视网膜电图(mfERG)测试均在正常范围内。连续的后续临床检查、视网膜成像、ffERG 和 mfERG 均显示疾病没有进展。初诊两年后,他出现了脊柱旁肿块,经活检发现是弥漫大 B 细胞淋巴瘤(DLBCL),并接受了化疗:结论:临床医生应该考虑那些出现鸟枪状脉络膜病变、HLA-A29阴性、有淋巴瘤病史或特征不典型的患者的BSCR伪装综合征。在本病例中,我们怀疑患者过去曾患低度 B 细胞淋巴瘤,化疗导致了慢性脉络膜病变。目前尚不清楚脉络膜受累是否会导致患者向高级别DLBCL转化。在治疗 DLBCL 的整个过程中,他的眼部症状一直没有活动。
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
Retinal Cases and Brief Reports
Retinal Cases and Brief Reports Medicine-Ophthalmology
CiteScore
2.10
自引率
0.00%
发文量
342
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