Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary and Alberta Precision Laboratories, Calgary, AB, Canada.
Histol Histopathol. 2022 May;37(5):405-413. doi: 10.14670/HH-18-435. Epub 2022 Feb 14.
Low-grade oncocytic tumor (LOT) of kidney has been recently proposed as a new renal entity. LOT was identified in the spectrum of oncocytic renal tumors with overlapping features between oncocytoma and eosinophilic chromophobe renal cell carcinoma, or it has been labelled as one of those entities in prior studies and in practice. LOT is often a single, relatively small tumor, found in a non-syndromic setting, but rare examples of multiple LOTs or admixed with other tumors have been found in patients with tuberous sclerosis complex. LOT typically has solid architecture, and it is composed of eosinophilic cells, with round to oval 'low-grade' nuclei, lacking irregularities and showing focal perinuclear halos. Sharp transition into edematous stromal areas, with scattered or loosely arranged cells are frequently found. LOT has a consistent immunohistochemical profile with diffuse reactivity for cytokeratin 7 and absent (or rarely weak) expression for CD117, a profile different from oncocytoma and eosinophilic chromophobe renal cell carcinoma. Similarly, in contrast to those entities, it also lacks or shows only weak expression for FOXI1. Recent studies have shown that LOT has a molecular/genetic profile different from other renal tumors, with frequent alterations affecting the MTOR/TSC pathway genes. LOT demonstrates either disomic pattern or deletions of 19p13, 19q13 and 1p36, and lacks complete chromosomal losses or gains. In all published studies to date, LOT has shown benign behavior. In this review, we summarize the evidence from recently published studies, which strongly supports the conclusion that LOT is a distinct and unique renal entity.
低级别嗜酸细胞瘤(LOT)是最近提出的一种新的肾脏实体。LOT 存在于嗜酸细胞瘤和嗜酸性染色性肾细胞癌之间重叠特征的嗜酸细胞瘤谱中,或者在之前的研究和实践中被标记为这些实体之一。LOT 通常是一个相对较小的单个肿瘤,发生在非综合征环境中,但在结节性硬化症患者中也发现了少数多发性 LOT 或与其他肿瘤混合的罕见病例。LOT 典型表现为实性结构,由嗜酸性细胞组成,圆形至椭圆形“低级别”核,无不规则性,并有局灶性核周晕。常可见到与水肿基质区呈锐利过渡,伴有散在或排列疏松的细胞。LOT 具有一致的免疫组织化学特征,对细胞角蛋白 7弥漫性反应,CD117 表达缺失(或很少为弱阳性),与嗜酸细胞瘤和嗜酸性染色性肾细胞癌的特征不同。同样,与这些实体相比,它也缺乏或仅显示微弱的 FOXI1 表达。最近的研究表明,LOT 的分子/遗传特征与其他肾脏肿瘤不同,常影响 MTOR/TSC 通路基因。LOT 表现为二倍体模式或 19p13、19q13 和 1p36 的缺失,缺乏完全的染色体缺失或获得。在迄今为止所有已发表的研究中,LOT 均表现出良性行为。在本综述中,我们总结了最近发表的研究证据,这些证据有力地支持了 LOT 是一种独特的肾脏实体的结论。