Anti-glomerular basement membrane disease with concomitant myeloperoxidase antibodies in a pediatric patient: a case report of presentation, treatment and outcome a rare disease.

Childhood kidney diseases Pub Date : 2026-02-01 Epub Date: 2025-11-08 DOI:10.3339/ckd.25.015
Yiressy Pina, Emily Frierson, John Hicks, Partha Chakraborty, Alvaro Orjuela, Amit Thakral
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Abstract

Anti-glomerular basement membrane disease (anti-GBMD) is a rare small-vessel vasculitis presenting as rapidly progressive glomerulonephritis and/or diffuse alveolar hemorrhage. A third of patients with anti-GBMD have antineutrophil cytoplasmic antibodies and are known as double-positive patients. There are a limited number of pediatric double-positive cases published in the literature. In this case report, we summarize the presentation, treatment, and outcome of a patient with anti-GBMD with both anti-myeloperoxidase and anti-GBM antibodies, highlighting the safe use of rituximab. We also describe atypical complications in our case, including significant weight loss of unclear etiology and development of recurrent episodes of acute pericalcific arthritis.

抗肾小球基底膜病伴髓过氧化物酶抗体的儿科患者:一个罕见疾病的表现、治疗和结果的病例报告
抗肾小球基底膜病(anti-GBMD)是一种罕见的小血管炎,表现为快速进展的肾小球肾炎和/或弥漫性肺泡出血。三分之一的抗gbmd患者有抗中性粒细胞细胞质抗体,被称为双阳性患者。文献中发表的儿科双阳性病例数量有限。在本病例报告中,我们总结了一位同时具有抗髓过氧化物酶和抗gbm抗体的抗gbmd患者的表现、治疗和结果,强调了利妥昔单抗的安全使用。我们还描述了本病例的非典型并发症,包括病因不明的显著体重减轻和急性关节炎复发发作的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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