Glomerulonephritis as a renal manifestation in a patient with systemic sclerosis overlapped with anti-neutrophil cytoplasmic antibody-associated vasculitis

Maysoun Kudsi, Yara Hodaifa, Raghad Tarcha, Rahaf Almajzoub, Suaad Hamsho, Afraa Ghazal
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Abstract

Systemic sclerosis (SSc) is a systemic immune disorder that may overlap with other rheumatologic disease; however, overlapping with antineutrophil cytoplasmic antibody-associated vasculitis is rare. A 28-year-old Syrian male patient with SSc diagnosed according to the American College of Rheumatology/European League against Rheumatism 2013 criteria with a disease duration of 4 years, was admitted to the hospital complaining of palpable purpura in the lower limbs and hemoptysis and later, a rise in creatinine level. Laboratory tests showed high levels of perinuclear antineutrophil cytoplasmic antibodies (p-ANCA). The renal biopsy results were consistent with the diagnosis of glomerulonephritis. He was treated with methylprednisolone, cyclophosphamide, and rituximab, as he was diagnosed with SSc overlapping antineutrophil cytoplasmic antibody-associated vasculitis. SSc most commonly renal manifestations are proliferative vasculopathy leading to scleroderma renal crisis. However, other types of renal involvement were also reported in SSc patients with comorbid autoimmune diseases such as glomerulonephritis and signs of concurrent vasculitis. SSc may overlap with rheumatoid arthritis, systemic lupus erythromatosus, polymyositis/dermatomyositis (PM/DM), and Sjogren Syndrome. Overlapping with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is mentioned in rare cases. The authors reported a rare case of overlapping SSc with antineutrophil cytoplasmic antibody-associated vasculitis with renal involvement. The authors revealed a rare case of overlapping SSc with antineutrophil cytoplasmic antibody-associated vasculitis with renal involvement. In SSc, renal involvement as glomerulonephritis is infrequent and should be detect in other rheumatologic disease such as systemic lupus erythematosus or antineutrophil cytoplasmic antibody-associated vasculitis.
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肾小球肾炎是一名系统性硬化症患者的肾脏表现,与抗中性粒细胞胞浆抗体相关性血管炎相重叠
系统性硬化症(SSc)是一种系统性免疫疾病,可能与其他风湿病重叠;但与抗中性粒细胞胞浆抗体相关性血管炎重叠的情况却很少见。 一名 28 岁的叙利亚男性患者根据美国风湿病学会/欧洲抗风湿病联盟 2013 年标准被诊断为 SSc,病程 4 年,入院时主诉下肢可触及紫癜、咯血,随后肌酐水平升高。实验室检查显示,患者体内存在高水平的核周抗中性粒细胞胞浆抗体(p-ANCA)。肾活检结果与肾小球肾炎的诊断一致。他被诊断为 SSc 合并抗中性粒细胞胞浆抗体相关性血管炎,因此接受了甲基强的松龙、环磷酰胺和利妥昔单抗治疗。 SSc 最常见的肾脏表现是导致硬皮病肾危象的增生性血管病变。不过,也有报道称,合并自身免疫性疾病(如肾小球肾炎)和并发血管炎症状的 SSc 患者也会出现其他类型的肾脏受累。SSc 可能与类风湿性关节炎、系统性红斑狼疮、多发性肌炎/皮肌炎(PM/DM)和 Sjogren 综合征重叠。与抗中性粒细胞胞浆抗体(ANCA)相关性血管炎重叠的病例很少见。作者报告了一例罕见的 SSc 与抗中性粒细胞胞浆抗体相关性血管炎重叠并累及肾脏的病例。 作者揭示了一例罕见的 SSc 与抗中性粒细胞胞浆抗体相关性血管炎重叠并累及肾脏的病例。在 SSc 中,肾脏受累为肾小球肾炎的情况并不常见,应在系统性红斑狼疮或抗中性粒细胞胞浆抗体相关性血管炎等其他风湿病中进行检测。
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