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病例报告:从IgA肾病到肺炎、阑尾周围脓肿、肺动脉高压和基底节钙化:一例儿童慢性活动性EB病毒感染病例

Case Report: From IgA nephropathy to pneumonia, periappendiceal abscess, pulmonary arterial hypertension, and basal ganglia calcification: a case of chronic active Epstein-Barr infection in a child.

作者信息

Fan Shuying, Wang Xin, Wei Ning, Zhou Qiumei, Wang Wenhong

机构信息

Department of Nephrology, Tianjin Children's Hospital, Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, China.

出版信息

Front Pediatr. 2025 Aug 4;13:1589151. doi: 10.3389/fped.2025.1589151. eCollection 2025.

Abstract

Chronic active Epstein-Barr virus infection (CAEBV) is a lymphoproliferative disorder characterized by persistent EBV infection, which can lead to multi-organ involvement. This case describes a child with CAEBV who initially presented with IgA nephropathy (IgAN) without characteristic infectious mononucleosis (IM) features. The patient initially presented with intermittent gross hematuria, Renal biopsy confirmed focal proliferative IgAN, and the child was treated with methylprednisolone pulse therapy followed by oral prednisone. During follow-up, the patient sequentially developed pneumonia caused by co-infection with EBV and , periappendiceal abscess, pancytopenia, Intermittently elevated peripheral blood EBV-DNA load, raising suspicion of CAEBV. Further investigations revealed the following findings: echocardiography demonstrated pulmonary arterial hypertension (PAH); cranial CT showed multiple bilateral basal ganglia calcifications; bone marrow biopsy detected EBV-DNA positivity (6.5 × 10³ copies/ml); renal tissue immunohistochemistry showed CD8+ cells (scattered, -50/HPF) and CD4+ cells (focal, -40/HPF), with negative LMP-1 but scattered EBER+ signals (-25/HPF). Based on persistently elevated peripheral blood EBV-DNA load, EBER-positive lymphocyte infiltration in renal tissue, evidence of multi-organ involvement, the diagnosis of CAEBV was established.

摘要

慢性活动性EB病毒感染(CAEBV)是一种以EB病毒持续感染为特征的淋巴增殖性疾病,可导致多器官受累。本病例描述了一名患有CAEBV的儿童,其最初表现为IgA肾病(IgAN),无典型传染性单核细胞增多症(IM)特征。该患者最初表现为间歇性肉眼血尿,肾活检确诊为局灶增生性IgAN,患儿接受了甲泼尼龙冲击治疗,随后口服泼尼松。在随访期间,患者相继出现由EB病毒合并感染引起的肺炎、阑尾周围脓肿、全血细胞减少,外周血EBV-DNA载量间歇性升高,引发了对CAEBV的怀疑。进一步检查发现以下结果:超声心动图显示肺动脉高压(PAH);头颅CT显示双侧基底节多发钙化;骨髓活检检测到EBV-DNA阳性(6.5×10³拷贝/ml);肾组织免疫组化显示CD8+细胞(散在,-50/HPF)和CD +细胞(局灶,-40/HPF),LMP-1阴性但有散在的EBER+信号(-25/HPF)。基于外周血EBV-DNA载量持续升高、肾组织中EBER阳性淋巴细胞浸润、多器官受累的证据,确诊为CAEBV。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/116b/12358464/393430fcdb20/fped-13-1589151-g001.jpg

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