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肾实质软斑病和巨细胞间质性肾炎:临床及组织学特征。两例报告并文献复习。

Renal parenchymal malacoplakia and megalocytic interstitial nephritis: clinical and histological features. Report of two cases and review of the literature.

作者信息

al-Sulaiman M H, al-Khader A A, Mousa D H, al-Swailem R Y, Dhar J, Haleem A

机构信息

Department of Nephrology, Riyadh Armed Forces Hospital, Saudi Arabia.

出版信息

Am J Nephrol. 1993;13(6):483-8. doi: 10.1159/000168668.

Abstract

We report 2 cases of acute renal failure caused by rare and closely related inflammatory conditions, i.e. renal parenchymal malacoplakia and megalocytic interstitial nephritis. We have discussed the clinical presentation, natural progression of the disease, the short- and longterm prognosis of the kidney, the histological appearances, the radiological features and the medical therapy together with a review of the literature.

摘要

我们报告了2例由罕见且密切相关的炎症性疾病引起的急性肾衰竭病例,即肾实质软斑病和巨细胞间质性肾炎。我们讨论了临床表现、疾病的自然进展、肾脏的短期和长期预后、组织学表现、放射学特征以及药物治疗,并对相关文献进行了综述。

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