Vanishing Kidney: On the Far End of the Spectrum of Xanthogranulomatous Pyelonephritis

被引：0

作者：

Amini, Fariba ^{[1
]}

Onur, Mehmet Ruhi ^{[2
]}

Kosemehmetoglu, Kemal ^{[3
,4
]}

机构：

[1] Guven Hosp, Dept Pathol, Ankara, Turkiye

[2] Hacettepe Univ, Dept Radiol, Fac Med, Ankara, Turkiye

[3] Hacettepe Univ, Dept Pathol, Fac Med, Ankara, Turkiye

[4] Hacettepe Univ, Dept Pathol, Gevher Nesibe Caddesi 1, TR-06230 Ankara, Turkiye

来源：

INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY | 2024年 / 32卷 / 02期

关键词：

kidney; Actinomyces; chronic kidney disease; EXPERIENCE;

D O I：

10.1177/10668969231171938

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

Xanthogranulomatous pyelonephritis (XGP) is a rare and severe form of chronic pyelonephritis associated with the destruction of the renal parenchyma and granulomatous inflammation with foamy lipid-laden macrophages resulting from urinary tract obstruction, nephrolithiasis, infection, diabetes, and immune compromise. Kidney parenchyma could be detected easily in XGP even if it is atrophic. However, here we present a 58-year-old man with XGP in which the renal parenchyma has near completely disappeared, which we referred to as the "vanishing kidney."

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收藏

页码：359 / 361

页数：3

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