首页> 外文期刊>Virchows Archiv: an international journal of pathology >Chromophobe renal cell carcinoma with microcystic and adenomatous arrangement and pigmentation--a diagnostic pitfall. Morphological, immunohistochemical, ultrastructural and molecular genetic report of 20 cases.
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Chromophobe renal cell carcinoma with microcystic and adenomatous arrangement and pigmentation--a diagnostic pitfall. Morphological, immunohistochemical, ultrastructural and molecular genetic report of 20 cases.

机译:具有微囊性和腺瘤性排列和色素沉着的发色肾细胞癌-诊断的陷阱。形态,免疫组化,超微结构和分子遗传学报告20例。

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摘要

We present clinical, morphological, immunohistochemical, ultrastructural and molecular genetic features of 20 cases of a peculiar form of chromophobe renal cell carcinoma (CRCC) with morphology differing from that of conventional CRCC. Microscopically, the typical features of the tumors were microcystic arrangement and formation of adenomatous structures. Microcystic areas were composed of smaller eosinophilic and bigger pale cells having cytological appearance typical of conventional CRCC. Cytological features of the adenomatous structures were mostly different from those of conventional CRCC. They had a typical columnar arrangement with nuclei positioned at the base of the glandular structures and a small amount of a deeply eosinophilic cytoplasm often endowed with brush border facing the lumen of the glands. In addition, all the tumors showed a brown pigmentation. The pigmentation was located mostly extracellularly, where it formed pools of heavy deposits. Microscopic calcifications present in all cases formed psammoma bodies or else the calcifications were more extensive and amorphous in shape. Ultrastructurally, the cells showed features characteristic of CRCC: typical cytoplasmic vesicles were 100-700 nm in size and mitochondria had tubulovesicular, lamellar or circular cristae. Some tumor cells contained dark, variously sized electron-dense pigment granules. Neither melanosomes nor membrane-bound neurosecretory granules were seen. Using fluorescence in-situ hybridization probes for chromosomes 1, 2, 6, 10, 13, 17 and 21, the tumors revealed massive loss of tested chromosomes typical for conventional CRCC. Monosomy of chromosomes 1, 2, 6, 10, 13 and 21 was found in 100, 36, 91, 82, 82, 82 and 64% of cases, respectively. None of the cases showed mutation of exons 9, 11, 13 and 17 of the c-kit gene. The important feature of pigmented microcystic chromophobe renal cell carcinoma is a relatively benign biological behavior and the absence of distant metastases and sarcomatoid transformation.
机译:我们介绍20例特殊形式的发色性肾细胞癌(CRCC)的临床,形态,免疫组织化学,超微结构和分子遗传学特征,其形态与常规CRCC不同。在显微镜下,肿瘤的典型特征是微囊排列和腺瘤结构的形成。微囊区域由较小的嗜酸性粒细胞和较大的苍白细胞组成,具有常规CRCC典型的细胞学外观。腺瘤结构的细胞学特征与常规CRCC的大多数不同。它们具有典型的柱状排列,核位于腺结构的底部,少量的深嗜酸性细胞质通常具有面向腺腔的刷状边界。另外,所有肿瘤均显示出褐色的色素沉着。色素沉着大部分位于细胞外,形成大量沉积物。在所有情况下都存在的微观钙化形成了肺腺瘤体,否则钙化更加广泛且形状无定形。在超微结构上,这些细胞显示出CRCC的特征:典型的细胞质囊泡大小为100-700 nm,线粒体具有肾小管,层状或圆形cr。一些肿瘤细胞含有深色,大小不同的电子致密颜料颗粒。既没有看到黑素体,也没有看到膜结合的神经分泌颗粒。使用针对1、2、6、10、13、17和21号染色体的荧光原位杂交探针,肿瘤显示出常规CRCC典型的受试染色体大量丢失。分别在100%,36%,91%,82%,82%,82%和64%的病例中发现了1、2、6、10、13和21号染色体的单体性。这些病例均未显示出c-kit基因外显子9、11、13和17的突变。色素性微囊发色团肾细胞癌的重要特征是相对良性的生物学行为,没有远处转移和肉瘤样转化。

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