Wang Huifang, Huang Yiqi, Jin Feng, Liu Xinxin
Department of Digestive System, Shaoxing Second Hospital, Shaoxing, Zhejiang, Zhejiang, China.
Department of Nephrology, Shaoxing Second Hospital, Shaoxing, Zhejiang, China.
Front Med (Lausanne). 2025 Aug 29;12:1621723. doi: 10.3389/fmed.2025.1621723. eCollection 2025.
Rituximab is widely used for autoimmune nephropathy. It depletes B cells, potentially increasing infection risk. Tuberculosis is a rare but severe complication of rituximab treatment. We report a case of liver tuberculosis in a patient with C1q nephropathy with Minimal Change Disease (MCD) treated with rituximab.
In March 2023, an 81-year-old male patient was admitted to Shaoxing Second Hospital with a 2-month history of bilateral lower extremity edema. He was diagnosed with C1q nephropathy with MCD through renal biopsy. After treatment with 2 g rituximab, his proteinuria was relieved. In October 2024, due to B-cell rebound, 0.5 g of rituximab was added. In December 2023, the patient visited our hospital due to a 7-day fever. Abdominal ultrasound revealed a non-uniform hypoechoic liver mass suspected to be an abscess. Empirical antibiotic treatment was ineffective and the condition worsened. A liver biopsy was immediately performed, and the pathology showed characteristic granulomatous inflammation and patchy coagulative necrosis. The patient was ultimately diagnosed with hepatic tuberculosis and received a 1-year anti-tuberculosis treatment, including rifampicin 450 mg qd, isoniazid 300 mg qd, pyrazinamide 1,500 mg qd, and ethambutol 1,000 mg qd. The patient's temperature returned to normal and abdominal pain was relieved on the third day of treatment. Two months later, a follow-up ultrasound showed a reduction in the left lobe liver mass, and an 8-month CT scan showed complete disappearance of the mass. The patient is currently under follow-up.
Rituximab may be an effective treatment option for C1q nephropathy with MCD. Although the risk of infection with rituximab is relatively low, rare infections such as tuberculosis still need to be vigilant, especially in elderly or immunocompromised patients. Additionally, we recommend routine screening for latent tuberculosis in elderly patients with nephropathy and hypogammaglobulinemia before rituximab treatment.
利妥昔单抗广泛用于自身免疫性肾病。它可消耗B细胞,可能增加感染风险。结核病是利妥昔单抗治疗罕见但严重的并发症。我们报告一例在用利妥昔单抗治疗的伴有微小病变性肾病(MCD)的C1q肾病患者中发生肝结核的病例。
2023年3月,一名81岁男性患者因双下肢水肿2个月入住绍兴第二医院。通过肾活检诊断为伴有MCD的C1q肾病。在用2g利妥昔单抗治疗后,他的蛋白尿得到缓解。2024年10月,由于B细胞反弹,加用了0.5g利妥昔单抗。2023年12月,患者因发热7天前来我院就诊。腹部超声显示肝脏有不均匀低回声肿块,怀疑是脓肿。经验性抗生素治疗无效,病情恶化。立即进行了肝活检,病理显示有特征性的肉芽肿性炎症和片状凝固性坏死。患者最终被诊断为肝结核,并接受了为期1年的抗结核治疗,包括利福平450mg每日一次、异烟肼300mg每日一次、吡嗪酰胺1500mg每日一次和乙胺丁醇1000mg每日一次。治疗第三天患者体温恢复正常,腹痛缓解。两个月后,随访超声显示左叶肝脏肿块缩小,8个月后的CT扫描显示肿块完全消失。患者目前正在接受随访。
利妥昔单抗可能是伴有MCD的C1q肾病的有效治疗选择。尽管利妥昔单抗的感染风险相对较低,但仍需警惕结核病等罕见感染,尤其是在老年或免疫功能低下的患者中。此外,我们建议在对患有肾病和低丙种球蛋白血症的老年患者进行利妥昔单抗治疗前,常规筛查潜伏性结核。