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显微镜下多血管炎以肾小管间质性肾炎为非典型表现。

Microscopic polyangiitis atypically presenting with tubulointerstitial nephritis.

作者信息

Wen Y K, Chen M L

机构信息

Department of Medicine, Changhua Christian Hospital, Changhua, Taiwan.

出版信息

Clin Nephrol. 2006 May;65(5):356-60. doi: 10.5414/cnp65356.

Abstract

A 65-year-old woman was admitted with a 4-week history of non-specific constitutional symptoms. Microscopic hematuria, proteinuria and mild renal insufficiency together with the presence of serum antineutrophil cytoplasmic antibodies prompted to perform a renal biopsy. The specimen showed tubulointerstitial nephritis without glomerular change. However, she developed purpura on lower limbs and hemoptysis, along with diffuse pulmonary infiltrates on chest radiograph, 2 weeks after admission. Skin and lung biopsies demonstrated leukocytoclastic vasculitis and diffuse alveolar hemorrhage, respectively. Microscopic polyangiitis was diagnosed based on clinical and pathological criteria. Clinical improvement occurred after intensive immunosuppressive therapy was given. This case illustrates an unusual renal presentation of tubulointerstitial nephritis in microscopic polyangiitis. The possible pathogenetic mechanism will be discussed.

摘要

一名65岁女性因4周的非特异性全身症状入院。镜下血尿、蛋白尿和轻度肾功能不全,以及血清抗中性粒细胞胞浆抗体的存在促使进行肾活检。标本显示为肾小管间质性肾炎,无肾小球改变。然而,入院2周后,她双下肢出现紫癜和咯血,胸部X线片显示弥漫性肺部浸润。皮肤和肺活检分别显示白细胞破碎性血管炎和弥漫性肺泡出血。根据临床和病理标准诊断为显微镜下多血管炎。给予强化免疫抑制治疗后临床症状改善。该病例说明了显微镜下多血管炎中肾小管间质性肾炎一种不寻常的肾脏表现。将讨论可能的发病机制。

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