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Glomerular sparing pattern in primary kidney neoplasms: clinical morphological and immunohistochemical study

机译:原发性肾肿瘤的肾小球保留模式:临床形态学和免疫组化研究

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摘要

Glomerular sparing (GS) is defined as a unique growth pattern in which tumor cells replace the majority of renal tubes and overrun intact glomeruli. This phenomenon has been well recognized by pathologists as a typical infiltrative pattern and some studies suggested it was an independent risk factor. Here, we study the clinical, pathological, and immunohistochemical features of primary kidney neoplasms with glomerular sparing pattern. We searched the archives of our pathology department for nephrectomy specimens and reviewed all pathology reports from 2009-2013. We selected cases with tumor and collected clinicopathological information, focusing on re-evaluation of cases with glomerular sparing pattern. To facilitate our study we performed immunohistochemical stains of PAX-8, p63, and InI-1 on selected cases. We selected a total of 204 nephrectomy cases in this study, including 163 cases of renal cell carcinoma; 37 cases of urothelial carcinoma; 4 cases from other categories (Wilms tumor, primary diffuse large B-cell lymphoma, angiolipoma, rhabdoid tumor). Finally, we identified 7 cases of primary kidney tumors with glomerular sparing pattern: 2 cases of clear cell renal cell carcinomas (ccRCC), 1 case of collecting duct carcinoma, 2 cases of urothelial carcinoma (UC), 1 case of diffuse large B-cell lymphoma and 1 case of malignant rhabdoid tumor. The primary kidney tumors with glomerular sparing pattern are rare and incidence in our study is <4% (7/204). There is no specificity for any tumor type, but more commonly seen in high grade UC rather than RCC. It can also be seen in rare neoplasms such as collecting duct carcinoma, lymphoma and malignant rhabdoid tumor. These GS cases need to be recognized as they are often associated with high grade, high stage, large tumor size, and worse prognosis.
机译:肾小球保留(GS)被定义为一种独特的生长方式,其中肿瘤细胞取代了大部分的肾管,并使完整的肾小球溢出。这种现象已被病理学家公认是典型的浸润方式,一些研究表明这是一个独立的危险因素。在这里,我们研究肾小球保留型的原发性肾脏肿瘤的临床,病理和免疫组织化学特征。我们在病理科的档案馆中搜索了肾切除术标本,并回顾了2009-2013年的所有病理报告。我们选择了肿瘤病例并收集了临床病理信息,重点是对肾小球保留型病例的重新评估。为了促进我们的研究,我们对部分病例进行了PAX-8,p63和InI-1的免疫组化染色。我们总共选择了204例肾切除术病例,其中包括163例肾细胞癌。尿路上皮癌37例;其他类别(Wilms肿瘤,原发性弥漫性大B细胞淋巴瘤,血管脂肪瘤,横纹肌瘤)中有4例。最后,我们确定了7例肾小球保留型原发性肾脏肿瘤:2例透明细胞肾细胞癌(ccRCC),1例收集导管癌,2例尿路上皮癌(UC),1例弥漫性大B-细胞淋巴瘤和恶性横纹肌瘤1例。具有肾小球保留型的原发性肾脏肿瘤很少见,在我们的研究中发生率<4%(7/204)。没有针对任何肿瘤类型的特异性,但更常见于高级UC而非RCC。在罕见的肿瘤中也可以看到它,例如收集导管癌,淋巴瘤和恶性横纹肌瘤。这些GS病例通常与高级别,高分期,大肿瘤大小和预后较差有关,因此需要得到认可。

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