Baba Füsun, Nanovic Lisa, Jaffery Jonathan B, Friedl Andreas
Department of Pathology and Laboratory Medicine, University of Wisconsin, Clinical Sciences Center K4/812, 600 Highland Avenue, Madison, WI 53562, USA.
Pathol Res Pract. 2006;202(7):555-9. doi: 10.1016/j.prp.2006.02.004. Epub 2006 May 5.
Karyomegalic tubulointerstitial nephritis is a rare disease of uncertain etiology, which leads to progressive renal failure. Here, we report on a 39-year-old patient who presented with asymptomatic progressive decline of renal function. Two sequential renal biopsies demonstrated chronic tubulointerstitial nephritis with bizarre and dramatic enlargement of proximal tubule epithelial cell nuclei - the hallmark of karyomegalic nephritis. Clinical and pathologic findings of this case are discussed in light of the available literature. The morphologic changes in this disease are highly characteristic if the pathologist is aware of this entity.
核肿大性肾小管间质性肾炎是一种病因不明的罕见疾病,可导致进行性肾衰竭。在此,我们报告一名39岁的患者,其肾功能呈无症状性进行性下降。两次连续的肾活检显示为慢性肾小管间质性肾炎,近端肾小管上皮细胞核出现怪异且显著的肿大,这是核肿大性肾炎的标志。结合现有文献对该病例的临床和病理结果进行了讨论。如果病理学家了解这种疾病,其形态学变化具有高度特征性。