Avacopan治疗复发性多软骨炎伴髓过氧化物酶-抗中性粒细胞细胞质抗体相关性血管炎1例。

Jack Tang Nguyen, Manish Anand
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引用次数: 0

摘要

背景:本病例报告描述了一例复发性多软骨炎患者的髓过氧化物酶抗中性粒细胞细胞质抗体相关血管炎并肾脏受累,并成功地用Avacopan治疗。虽然复发性多软骨炎与抗中性粒细胞细胞质抗体相关的血管炎有关,但重叠可导致严重的器官受累,特别是肾脏损害进展为终末期肾脏疾病。本病例提供了一个独特的机会来评估Avacopan作为治疗髓过氧化物酶-抗中性粒细胞细胞质抗体相关血管炎的替代治疗选择的潜在作用,在复发性多软骨炎的背景下,突出了治疗挑战的积极肾反应。病例总结:这是一个69岁的白人妇女,她以4周的耳廓软骨炎性多软骨炎病史就诊于我院急诊科,并伴有急性肾损伤。入院时,血清肌酐升高至4.0 mg/dL,第6天逐渐升高至6.07 mg/dL。肾活检显示坏死和新月形肾小球肾炎影响超过50%的肾小球。患者接受静脉注射甲基强的松2500mg 3天,随后口服强的松。诱导治疗包括静脉环磷酰胺诱导,计划共2剂,然后过渡到利妥昔单抗。然而,由于过敏反应,患者无法耐受利妥昔单抗,因此继续静脉注射环磷酰胺共6次剂量(累计剂量3000 mg)。在持续性急性肾损伤的情况下,在诊断后3个月加入Avacopan。维持治疗包括硫唑嘌呤和Avacopan。强的松在6个月时逐渐减少。结论:Avacopan可能对抗中性粒细胞细胞质抗体相关血管炎合并复发性多软骨炎的治疗有益,特别是在保存肾功能至关重要的情况下。进一步的研究对于验证这些发现和完善此类复杂病例的治疗方案至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Avacopan in the treatment of relapsing polychondritis with myeloperoxidase-antineutrophil cytoplasmic antibody associated vasculitis: A case report.

Background: This case report describes myeloperoxidase-anti-neutrophil cytoplasmic antibody associated vasculitis with kidney involvement in a patient with relapsing polychondritis, which was successfully treated with Avacopan. Although relapsing polychondritis has been associated with anti-neutrophil cytoplasmic antibody-associated vasculitis, overlap can result in severe organ involvement, particularly renal damage progressing to end-stage kidney disease. This case presents a unique opportunity to evaluate the potential role of Avacopan as an alternative therapeutic option in managing myeloperoxidase-anti-neutrophil cytoplasmic antibody-associated vasculitis in the context of relapsing polychondritis highlighting a positive renal response despite treatment challenges.

Case summary: This is a case of a 69-year-old Caucasian woman who presented to our hospital's emergency department with a 4 week history of inflammatory polychondritis affecting the auricular cartilage, accompanied by acute kidney injury. On admission, serum creatinine was elevated at 4.0 mg/dL, which progressively increased to 6.07 mg/dL on day 6. The renal biopsy revealed necrotizing and crescentic glomerulonephritis affecting more than 50% of the glomeruli. She was treated with a total of 2500 mg intravenous methylprednisolone over 3 days followed by oral prednisone. Induction treatment included intravenous cyclophosphamide induction, with plans for a total of 2 doses followed by transition to rituximab. However the patient was unable to tolerate rituximab due to allergic reaction so intravenous cyclophosphamide was continued for a total of 6 doses (cumulative dose 3000 mg). In the setting of persistent acute kidney injury, Avacopan was added to the regimen 3 months after diagnosis. Maintenance therapy included azathioprine in addition to Avacopan. Prednisone gradually tapered off at 6 months.

Conclusion: Avacopan may be beneficial in treating anti-neutrophil cytoplasmic antibody-associated vasculitis with coexisting relapsing polychondritis, especially in cases where preservation of kidney function is critical. Further research will be essential to validate these findings and refine treatment protocols for such complex cases.

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