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肼屈嗪诱发的孤立性狼疮性肾炎。

Hydralazine-Induced Isolated Lupus Nephritis.

作者信息

Khan Naseer, Reichel Ronald, Khurshid Ayesha, Tso Katie, Broussard Joan, Dass Amrika

机构信息

Department of Nephrology, Ochsner Clinic Foundation, Baton Rouge, LA.

The Institute for Evidence-Based Reform, Baton Rouge, LA.

出版信息

Ochsner J. 2020 Summer;20(2):187-192. doi: 10.31486/toj.18.0128.

Abstract

Hydralazine has been known to cause multiple side effects, both localized and systemic. The literature includes case reports of systemic vasculitis caused by hydralazine. A 79-year-old male with stage 3 chronic kidney disease attributable to hypertension and type 2 diabetes was started on hydralazine to control his hypertension. Three weeks after starting hydralazine, the patient developed nephrotic syndrome and acute kidney injury with progressively worsening proteinuria. Pathologic evaluation of the kidney tissue revealed that the patient had lupus nephritis. Immunologic markers confirmed hydralazine-induced lupus nephritis with positive antihistone antibodies. No evidence of systemic vasculitis was found. The patient's hydralazine was stopped, and the patient was treated with immunosuppressive therapy. After 7 months of immunosuppressive therapy, the patient achieved complete remission of lupus nephritis. Isolated renal disease induced by hydralazine as part of drug-induced lupus is uncommon. Our patient developed isolated classic lupus nephritis after hydralazine therapy with no associated systemic vasculitis. Treatment required stopping the hydralazine and initiating systemic immunosuppressive therapy to achieve complete remission.

摘要

已知肼屈嗪会引起多种副作用,包括局部和全身的副作用。文献中有关于肼屈嗪引起系统性血管炎的病例报告。一名79岁男性,因高血压和2型糖尿病导致3期慢性肾脏病,开始使用肼屈嗪控制高血压。开始使用肼屈嗪三周后,患者出现肾病综合征和急性肾损伤,蛋白尿逐渐加重。肾脏组织的病理评估显示患者患有狼疮性肾炎。免疫标志物证实为肼屈嗪诱导的狼疮性肾炎,抗组蛋白抗体呈阳性。未发现系统性血管炎的证据。停用了患者的肼屈嗪,并对患者进行免疫抑制治疗。经过7个月的免疫抑制治疗,患者的狼疮性肾炎完全缓解。作为药物性狼疮一部分的肼屈嗪诱导的孤立性肾脏疾病并不常见。我们的患者在接受肼屈嗪治疗后出现了孤立性典型狼疮性肾炎,无相关系统性血管炎。治疗需要停用肼屈嗪并启动全身免疫抑制治疗以实现完全缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/411d/7310176/65cc07415641/toj-18-0128-figure1.jpg

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