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罕见巧合:甲型流感相关急性肾损伤并发管型肾病和淋巴瘤浸润

Unusual Coincidence: Concurrent Cast Nephropathy and Lymphoma Infiltration in an Influenza A-Associated Acute Kidney Injury.

作者信息

Lee Wan-Ching, Tsai Chun-Kuang, Li Szu-Yuan

机构信息

Division of Nephrology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei 11217, Taiwan.

Division of Hematology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei 11217, Taiwan.

出版信息

Case Rep Nephrol. 2024 Mar 1;2024:5524746. doi: 10.1155/2024/5524746. eCollection 2024.

DOI:10.1155/2024/5524746
PMID:38463384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10923615/
Abstract

Acute kidney injury (AKI) poses a substantial challenge in the management of lymphoma patients and is frequently associated with diverse causative factors. Herein, we report an illustrative case involving a 47-year-old male with influenza A infection who developed severe AKI, which was incongruent with his medical history. Laboratory investigations disclosed aberrant immunoglobulin levels and urinary protein excretion, prompting further evaluation. A renal biopsy revealed the presence of infiltrating lymphoid cells and cast nephropathy, raising suspicion of an underlying hematological disorder. A comprehensive diagnostic workup, including positron emission tomography imaging and bone marrow biopsy, culminated in the definitive diagnosis of splenic marginal zone lymphoma. This case highlights the crucial significance of including lymphoma-associated kidney disorders in the evaluation of unexplained AKI, particularly when encountering unconventional clinical and laboratory results. Swift and precise intervention is of utmost importance in attaining positive results in these rare and complex clinical situations. This study underscores the persistent concern of AKI in lymphoma patients, with lymphocytic infiltration and cast nephropathy as notable elements contributing to the intricate nature of this condition.

摘要

急性肾损伤(AKI)在淋巴瘤患者的管理中构成了重大挑战,且常常与多种致病因素相关。在此,我们报告一例典型病例,一名47岁男性感染甲型流感后发生了严重的AKI,这与他的病史不符。实验室检查发现免疫球蛋白水平异常和尿蛋白排泄异常,促使进一步评估。肾活检显示有浸润性淋巴细胞和管型肾病,这引发了对潜在血液系统疾病的怀疑。包括正电子发射断层扫描成像和骨髓活检在内的全面诊断检查最终确诊为脾边缘区淋巴瘤。该病例凸显了在评估不明原因的AKI时纳入淋巴瘤相关肾脏疾病的至关重要性,尤其是在遇到非常规的临床和实验室结果时。在这些罕见且复杂的临床情况下,迅速而精确的干预对于取得积极结果至关重要。本研究强调了淋巴瘤患者中AKI这一持续存在的问题,淋巴细胞浸润和管型肾病是导致这种情况复杂性的显著因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/996c6cfa2b89/CRIN2024-5524746.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/118605be760a/CRIN2024-5524746.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/0d0bb5c03338/CRIN2024-5524746.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/996c6cfa2b89/CRIN2024-5524746.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/118605be760a/CRIN2024-5524746.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/0d0bb5c03338/CRIN2024-5524746.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d28/10923615/996c6cfa2b89/CRIN2024-5524746.003.jpg

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