Orbital mass as the presenting symptom of diffuse large B-cell lymphoma causing spontaneous tumor lysis syndrome and rapid multisystem organ failure.

Pub Date : 2024-10-01 Epub Date: 2023-07-27 DOI:10.1080/01676830.2023.2240410
Steven S Bae, Steve Rasmussen, David J A Plemel
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Abstract

A 68-year-old male presented with a one-month history of progressive proptosis and vision loss in the left eye. Examination of the left eye showed visual acuity of NLP, marked relative proptosis of 10 mm, and complete external ophthalmoplegia. CT orbits showed an extensive left orbital lesion with proptosis. Urgent orbital biopsy was undertaken. Intraoperatively, the patient developed new atrial flutter and fever. Bloodwork revealed metabolic derangements suggestive of tumor lysis syndrome. Systemic evaluation revealed a large tumor burden involving the retroperitoneal space. Histopathology of the orbital specimen showed non-germinal center diffuse large B-cell lymphoma. The patient passed away 3 days postoperatively due to rapidly progressive multisystem organ failure. Our case demonstrates an unusually aggressive presentation of DLBCL in which orbital mass was the first presentation of spontaneous tumor lysis syndrome owing to large systemic tumor burden.

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以眼眶肿块为首发症状的弥漫大B细胞淋巴瘤导致自发性肿瘤溶解综合征和多系统器官迅速衰竭。
一名 68 岁的男性患者因左眼进行性突眼和视力下降就诊一个月。左眼检查显示视力为 NLP,眼球明显相对突出 10 毫米,完全性外眼球麻痹。眼眶 CT 显示左眼眶广泛病变并伴有突眼。紧急进行了眼眶活检。术中,患者出现新的心房扑动和发热。血液检查发现代谢紊乱,提示肿瘤溶解综合征。全身评估显示,腹膜后间隙存在巨大肿瘤。眼眶标本的组织病理学显示为非芽胞中心弥漫大B细胞淋巴瘤。术后3天,患者因快速进展的多系统器官衰竭而去世。我们的病例表明,眼眶肿块是DLBCL的一种异常侵袭性表现,它是自发性肿瘤溶解综合征的首发症状,原因是全身肿瘤负荷较大。
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