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当一切都崩溃时我们能做什么?塌陷性肾小球病合并系统性红斑狼疮伴弥漫性肺泡出血的致命结局:病例报告

What Can We Do When All Collapses? Fatal Outcome of Collapsing Glomerulopathy and Systemic Lupus Erythematosus With Diffuse Alveolar Hemorrhage: Case Report.

作者信息

Pinto H, Leal R, Rodrigues L, Santos L, Romãozinho C, Macário F, Alves R, Pratas J, Sousa V, Marinho C, Prado E Castro L, Costa F, Campos M, Mota A, Figueiredo A

机构信息

Nephrology Department, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.

Nephrology Department, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.

出版信息

Transplant Proc. 2017 May;49(4):913-915. doi: 10.1016/j.transproceed.2017.03.007.

Abstract

INTRODUCTION

Collapsing glomerulopathy (CG) is a rare form of glomerular injury. Although commonly associated with human immunodeficiency virus (HIV) infection, it can occur in association with systemic lupus erythematosus (SLE).

CASE REPORT

We present the case of a 50-year-old man, with chronic kidney disease secondary to focal and segmental glomerulosclerosis, who received a cadaveric kidney transplant in 2007. There were no relevant intercurrences until May 2015, when he presented with nephrotic range proteinuria (± 4 g/d). A graft biopsy was performed and it did not show any significant pathological changes. In September, he developed a full nephrotic syndrome (proteinuria 19 g/d) and a graft biopsy was repeated. CG features were evident with a rich immunofluorescence. Antinuclear antibodies (ANA) and anti-double-stranded DNA (anti-dsDNA) antibodies were positive; the remaining immunologic study was normal. Viral markers for HIV, hepatitis C virus (HCV), and hepatitis B virus (HBV) were negative. The patient was treated with corticosteroid pulses and plasmapheresis (seven treatments). A rapid deterioration of kidney function was seen and he became dialysis dependent. He was discharged with a low-dose immunosuppressive treatment. In October, he was hospitalized with diffuse alveolar hemorrhage (DAH). The auto-immune study was repeated, revealing complement consumption and positive titers of ANA and Anti-dsDNA antibodies. Anti-neutrophil cytoplasmic antibodies (ANCAs) and antiglomerular basement membrane antibody (anti-GBM) were negative. Treatment with intravenous corticosteroids, plasmapheresis, and human immunoglobulin was ineffective and the outcome was fatal.

CONCLUSION

This case report highlights the possible association of CG and SLE. To our knowledge, it is the first case of SLE presenting with CG and DAH, with the singularity of occurring in a kidney transplant recipient receiving immunosuppression.

摘要

引言

塌陷性肾小球病(CG)是一种罕见的肾小球损伤形式。虽然它通常与人类免疫缺陷病毒(HIV)感染相关,但也可与系统性红斑狼疮(SLE)相关联。

病例报告

我们报告一例50岁男性病例,该患者因局灶节段性肾小球硬化继发慢性肾脏病,于2007年接受了尸体肾移植。直到2015年5月之前都没有相关并发情况,当时他出现了肾病范围蛋白尿(±4g/d)。进行了移植肾活检,未显示任何显著病理变化。9月,他发展为完全肾病综合征(蛋白尿19g/d),并再次进行了移植肾活检。CG特征明显,免疫荧光丰富。抗核抗体(ANA)和抗双链DNA(抗dsDNA)抗体呈阳性;其余免疫学检查正常。HIV、丙型肝炎病毒(HCV)和乙型肝炎病毒(HBV)的病毒标志物均为阴性。患者接受了大剂量糖皮质激素冲击治疗和血浆置换(7次治疗)。肾功能迅速恶化,他开始依赖透析。出院时接受低剂量免疫抑制治疗。10月,他因弥漫性肺泡出血(DAH)住院。再次进行自身免疫检查,发现补体消耗以及ANA和抗dsDNA抗体滴度呈阳性。抗中性粒细胞胞浆抗体(ANCA)和抗肾小球基底膜抗体(抗GBM)均为阴性。静脉注射糖皮质激素、血浆置换和人免疫球蛋白治疗均无效,最终患者死亡。

结论

本病例报告强调了CG与SLE之间可能存在的关联。据我们所知,这是首例SLE合并CG和DAH的病例,其独特之处在于发生在一名接受免疫抑制治疗的肾移植受者身上。

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