Recurrent Spontaneous Tumor Lysis Syndrome in Undiagnosed Follicular T-Cell Lymphoma.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-02-21 eCollection Date: 2025-01-01 DOI:10.1159/000544865
Feehaan H Sultan, Priya K Jindal, Zeeshaan H Sultan, Nahush R Bansal, Shuhao Qiu
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引用次数: 0

Abstract

Introduction: Spontaneous tumor lysis syndrome (TLS) is a rare, life-threatening metabolic complication that typically occurs in malignancies with high tumor burden. Early recognition is critical, even in the absence of a known malignancy, to prevent severe outcomes.

Case presentation: We report the case of an 89-year-old male with a history of chronic kidney disease, hyperparathyroidism, and myasthenia gravis, who experienced three episodes of TLS within 1 month. Initially, his metabolic disturbances were misattributed to dehydration. During his second admission, imaging revealed extensive lymphadenopathy, and a lymph node biopsy confirmed follicular helper T-cell lymphoma before his third hospitalization. Despite aggressive treatment, he developed metabolic encephalopathy and lost his decision-making capacity, while his family declined palliative care discussions.

Conclusion: This case highlights the importance of considering TLS in patients with unexplained hyperkalemia, hyperuricemia, and hyperphosphatemia, even in the absence of a malignancy diagnosis. Early diagnosis and multidisciplinary care are essential to improve outcomes.

未确诊滤泡性t细胞淋巴瘤复发性自发肿瘤溶解综合征。
自发性肿瘤溶解综合征(TLS)是一种罕见的危及生命的代谢并发症,通常发生在高肿瘤负担的恶性肿瘤中。即使在没有已知恶性肿瘤的情况下,早期识别对于预防严重后果也是至关重要的。病例介绍:我们报告一例89岁男性,有慢性肾脏疾病、甲状旁腺功能亢进和重症肌无力病史,在1个月内经历了3次TLS发作。起初,他的代谢紊乱被误认为是脱水造成的。第二次入院时,影像学显示广泛的淋巴结病变,第三次住院前淋巴结活检证实滤泡辅助t细胞淋巴瘤。尽管进行了积极的治疗,他还是患上了代谢性脑病,失去了决策能力,而他的家人拒绝讨论姑息治疗。结论:本病例强调了在不明原因的高钾血症、高尿酸血症和高磷血症患者中考虑TLS的重要性,即使没有恶性诊断。早期诊断和多学科治疗对于改善预后至关重要。
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
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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