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利妥昔单抗诱发生发中心进行性转化免疫球蛋白G4相关性疾病血清病:一例报告

Rituximab-induced serum sickness in progressive transformation of germinal centers immunoglobulin G4-related disease: a case report.

作者信息

Kumar Sharanya, Tuli Rahul, Seylani Allen, Abedi Eric, Friedman Alexander

机构信息

Internal Medicine, Riverside University Health System (RUHS), Moreno Valley, USA.

School of Medicine, University of California, Riverside, Riverside, USA.

出版信息

J Med Case Rep. 2025 Apr 19;19(1):181. doi: 10.1186/s13256-025-05222-1.

Abstract

INTRODUCTION

Serum sickness, a type III hypersensitivity reaction, can arise from various triggers such as vaccines, anti-venoms, and certain medications, particularly monoclonal antibodies. Rituximab, a monoclonal antibody targeting CD20 on B-cells, is known to induce a subtype of this reaction called rituximab-induced serum sickness, which primarily affects those with rheumatologic diseases.

CASE PRESENTATION

A 34-year-old Mexican-American female patient with focal segmental glomerulosclerosis was treated with rituximab for concomitant immunoglobulin G4-related disease. After her third infusion, she developed a rash, myalgias, arthralgias, and proteinuria, leading to a diagnosis of rituximab-induced serum sickness, which resolved with a prednisone taper.

CONCLUSION

Serum sickness should be considered as a potential differential diagnosis in patients exhibiting nonspecific systemic symptoms and dermatologic manifestations following exposure to a triggering factor, such as a newly administered monoclonal antibody medication. This is the first known case of rituximab-induced serum sickness in the context of immunoglobulin G4-related disease.

摘要

引言

血清病是一种III型超敏反应,可由多种触发因素引起,如疫苗、抗蛇毒血清和某些药物,尤其是单克隆抗体。利妥昔单抗是一种靶向B细胞上CD20的单克隆抗体,已知可诱发这种反应的一种亚型,称为利妥昔单抗诱导的血清病,主要影响患有风湿性疾病的患者。

病例介绍

一名34岁患有局灶节段性肾小球硬化的墨西哥裔美国女性患者因合并免疫球蛋白G4相关疾病接受利妥昔单抗治疗。在第三次输注后,她出现了皮疹、肌痛、关节痛和蛋白尿,最终被诊断为利妥昔单抗诱导的血清病,通过逐渐减少泼尼松剂量后病情得到缓解。

结论

对于在接触触发因素(如新使用的单克隆抗体药物)后出现非特异性全身症状和皮肤表现的患者,应考虑血清病作为一种潜在的鉴别诊断。这是已知的第一例在免疫球蛋白G4相关疾病背景下发生的利妥昔单抗诱导的血清病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75c/12009516/a8823db9e115/13256_2025_5222_Fig1_HTML.jpg

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