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对一名双侧肾嗜酸细胞瘤患者的11个肿瘤进行1号、2号、6号、10号和17号染色体着丝粒探针的间期细胞遗传学分析。

Interphase cytogenetic analysis with centromeric probes for chromosomes 1, 2, 6, 10, and 17 in 11 tumors from a patient with bilateral renal oncocytosis.

作者信息

Cossu-Rocca Paolo, Eble John N, Zhang Shaobo, Bonsib Stephen M, Martignoni Guido, Brunelli Matteo, Cheng Liang

机构信息

Department of Pathology and Laboratory Medicine, Indiana University, Indianapolis, IN, USA.

出版信息

Mod Pathol. 2008 Apr;21(4):498-504. doi: 10.1038/modpathol.2008.16. Epub 2008 Feb 8.

Abstract

Renal oncocytosis is characterized by the presence of multiple tumors with oncocytic features, often associated with small clusters of tubule-like structures with oncocytic change. The morphologic features of the oncocytic nodules encompass a spectrum of appearances, with patterns typical of renal oncocytoma or classic chromophobe renal cell carcinoma, as well as 'hybrid' tumors with features resembling both oncocytoma and chromophobe renal cell carcinoma. We utilized interphase cytogenetic methods to study 11 tumors from the kidneys of a 45-year-old woman. The tumors included morphologically classical oncocytomas and 'hybrid' tumors with features reminiscent of chromophobe carcinoma. The kidneys also showed foci of oncocytic change in renal tubules. Fluorescence in situ hybridization was performed with centromeric probes for chromosomes 1, 2, 6, 10, and 17 in each of the 11 tumors to determine whether or not there were losses of the chromosomes that are most frequently lost in chromophobe renal cell carcinomas. Neoplastic nuclei from each tumor were evaluated for the number of hybridization signals and scored according to the percentage of nuclei with one, two, and three or more signals. The normal renal parenchyma surrounding the tumors was used as control tissue. All 11 tumors from this patient with renal oncocytosis showed no loss of any of the chromosomes 1, 2, 6, 10, or 17, a pattern identical to that found in normal control tissues. These observations weigh against the concept that hybrid tumors of oncocytosis are closely related to chromophobe renal cell carcinoma.

摘要

肾嗜酸细胞瘤的特征是存在多个具有嗜酸细胞特征的肿瘤,常伴有小簇具有嗜酸细胞改变的小管样结构。嗜酸细胞结节的形态学特征呈现出一系列表现,具有肾嗜酸细胞瘤或经典嫌色肾细胞癌的典型模式,以及兼具嗜酸细胞瘤和嫌色肾细胞癌特征的“混合”肿瘤。我们采用间期细胞遗传学方法研究了一名45岁女性肾脏的11个肿瘤。这些肿瘤包括形态学上典型的嗜酸细胞瘤和具有类似嫌色癌特征的“混合”肿瘤。肾脏还显示肾小管有嗜酸细胞改变灶。对11个肿瘤中的每一个进行了荧光原位杂交,使用针对染色体1、2、6、10和17的着丝粒探针,以确定是否存在嫌色肾细胞癌中最常丢失的染色体缺失情况。评估每个肿瘤的肿瘤细胞核杂交信号数量,并根据具有一个、两个和三个或更多信号的细胞核百分比进行评分。肿瘤周围的正常肾实质用作对照组织。该肾嗜酸细胞瘤患者的所有11个肿瘤均未显示染色体1、2、6、10或17中的任何一条缺失,这一模式与正常对照组织中发现的模式相同。这些观察结果不支持嗜酸细胞瘤混合肿瘤与嫌色肾细胞癌密切相关的观点。

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