Department of Nephrology, Shengjing Hospital of China Medical University, 36 Sanhao Street, Shenyang, 110004, China.
BMC Infect Dis. 2023 May 2;23(1):272. doi: 10.1186/s12879-023-08232-w.
The renal involvement of brucellosis is not common. Here we reported a rare case of chronic brucellosis accompanied by nephritic syndrome, acute kidney injury, the coexistence of cryoglobulinemia and antineutrophil cytoplasmic autoantibodies (ANCA) associated vasculitis (AAV) superimposed on iliac aortic stent implantation. The diagnosis and treatment of the case are instructive.
A 49-year-old man with hypertension and iliac aortic stent implantation was admitted for unexplained renal failure with signs of nephritic syndrome, congestive heart failure, moderate anemia and livedoid change in the left sole with pain. His past history included chronic brucellosis and he just underwent the recurrence and completed the 6 weeks of antibiotics treatment. He demonstrated positive cytoplasmic/proteinase 3 ANCA, mixed type cryoglobulinemia and decreased C3. The kidney biopsy revealed endocapillary proliferative glomerulonephritis with a small amount of crescent formation. Immunofluorescence staining revealed only C3-positive staining. In accordance with clinical and laboratory findings, post-infective acute glomerulonephritis superimposed with AAV was diagnosed. The patient was treated with corticosteroids and antibiotics and sustained alleviation of renal function and brucellosis was achieved during the course of a 3-month follow-up.
Here we describe the diagnostic and treatment challenge in a patient with chronic brucellosis related glomerulonephritis accompanied by the coexistence of AAV and cryoglobulinemia. Renal biopsy confirmed the diagnosis of postinfectious acute glomerulonephritis overlapping with ANCA related crescentic glomerulonephritis, which was not ever reported in the literature. The patient showed a good response to steroid treatment which indicated the immunity-induced kidney injury. Meanwhile, it is essential to recognize and actively treat the coexisting brucellosis even when there are no clinical signs of the active stage of infection. This is the critical point for a salutary patient outcome for brucellosis associated renal complications.
布鲁氏菌病的肾脏受累并不常见。在这里,我们报告了一例罕见的慢性布鲁氏菌病合并肾病综合征、急性肾损伤、冷球蛋白血症和抗中性粒细胞胞质抗体(ANCA)相关血管炎(AAV)的病例,该病例继发于髂主动脉支架植入术后。该病例的诊断和治疗具有指导意义。
一名 49 岁男性,患有高血压和髂主动脉支架植入术,因不明原因的肾衰竭伴有肾病综合征、充血性心力衰竭、中度贫血和左足底疼痛性淤血性改变而入院。他的既往病史包括慢性布鲁氏菌病,且刚刚经历了复发并完成了 6 周的抗生素治疗。他表现为细胞质/蛋白酶 3 ANCA 阳性、混合冷球蛋白血症和 C3 降低。肾活检显示为毛细血管内增生性肾小球肾炎,伴有少量新月体形成。免疫荧光染色仅显示 C3 阳性染色。根据临床和实验室检查结果,诊断为感染后急性肾小球肾炎合并 AAV。患者接受了皮质类固醇和抗生素治疗,在 3 个月的随访过程中肾功能持续缓解,布鲁氏菌病也得到了控制。
本文描述了一例慢性布鲁氏菌病相关肾小球肾炎患者的诊断和治疗挑战,该患者同时存在 AAV 和冷球蛋白血症。肾活检证实了感染后急性肾小球肾炎重叠 ANCA 相关新月体性肾小球肾炎的诊断,这在文献中从未报道过。患者对类固醇治疗反应良好,表明免疫诱导的肾损伤。同时,即使没有感染活动期的临床症状,也需要认识并积极治疗共存的布鲁氏菌病。这是布鲁氏菌病相关肾并发症患者获得良好预后的关键。