Lacrimal sac diffuse large B-cell lymphoma presenting as sudden-onset binocular diplopia

Antoine Jeri-Yabar, Liliana Vittini-Hernandez, Bharati Dev, Marissa Patel, Meihuan Lin
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Abstract

Introduction: Diffuse large B-cell lymphoma (DLBCL) is a prevalent subtype of non-Hodgkin lymphoma (NHL) affecting predominantly elderly individuals. Case description: A 68-year-old man with a history of hypertension, hyperlipidaemia and a small pituitary gland tumour presented with sudden-onset binocular diplopia and right-eye blurry vision. A magnetic resonance imaging (MRI) of the brain revealed enhancing soft tissue in the right superolateral orbit inseparable from the lacrimal gland, extending medially to the right superior rectus muscle and soft tissue. Further scanning showed widespread metastasis to the bilateral retroperitoneal lymph nodes, adrenal gland, spine and lymph nodes in the neck. A biopsy of the lacrimal gland confirmed DLBCL. Conclusion: Primary lacrimal gland DLBCL is a rare and delayed diagnosis that often stems from the resemblance of its clinical manifestations to more benign conditions such as dacryocystitis, dacryostenosis or mucocele. Timely recognition and accurate diagnosis are essential for initiating appropriate treatment and improving patient outcomes.
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泪囊弥漫性大 B 细胞淋巴瘤表现为突发性双眼复视
导言:弥漫大 B 细胞淋巴瘤(DLBCL)是非霍奇金淋巴瘤(NHL)的一种流行亚型,主要影响老年人。病例描述一名有高血压、高脂血症和垂体小肿瘤病史的 68 岁男子突然出现双眼复视和右眼视力模糊。脑部磁共振成像(MRI)显示,右侧眼眶上外侧软组织增强,与泪腺密不可分,向内侧延伸至右侧上直肌和软组织。进一步扫描显示,肿瘤广泛转移至双侧腹膜后淋巴结、肾上腺、脊柱和颈部淋巴结。泪腺活检证实为 DLBCL。结论原发性泪腺DLBCL是一种罕见的延误诊断病症,其临床表现往往与泪囊炎、泪管狭窄症或粘液囊肿等良性病症相似。及时识别和准确诊断对于开始适当治疗和改善患者预后至关重要。
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