Krishnan Bhuvaneswari, Truong Luan D
Department of Pathology, Veterans Affairs Medical Center, Houston, TX 77030, USA.
Hum Pathol. 2002 Jan;33(1):68-79. doi: 10.1053/hupa.2002.30210.
Several unsettled histogenetic, nosologic and diagnostic considerations for renal epithelial tumors may have ultrastructural ramifications. Yet, a comprehensive electron microscopic study of renal epithelial neoplasms, in light of the recent classification, is not available. The ultrastructural findings from fifty-five renal epithelial neoplasms [31 clear cell renal cell carcinomas (RCC), 11 papillary RCC, 5 chromophobe RCC, 3 sarcomatoid RCC and 5 oncocytomas] were correlated with their light microscopic appearance. Clear cell RCC showed long microvilli similar to the brush border of the normal proximal tubules, with abundant cytoplasmic lipid and glycogen. Papillary RCC showed variably sized microvilli, and small amounts of cytoplasmic lipid, but no glycogen. Chromophobe RCC showed many cytoplasmic vesicles and abnormal mitochondria, with rare short and stubby microvilli. Renal oncocytoma showed many mitochondria with a few vesicles in the apical portion of the cytoplasm and rare short and stubby microvilli. The eosinophilic cell variants of clear cell RCC, papillary RCC and chromophobe RCC showed ultrastructural features similar to those of their respective prototypes, except for an increased numbers of mitochondria in the cytoplasm. One sarcomatoid clear cell RCC showed skeletal muscle differentiation. Two types of cytoplasmic inclusions, i.e. hyaline globules and granules similar to those in the Paneth cells (PC-like granules) were identified only in clear cell RCC, which displayed distinctive ultrastructural features. The current EM study demonstrates distinctive ultrastructural features of renal epithelial neoplasms. The findings lend additional support to the current classification of the pertinent tumor types, facilitate the differential diagnoses, and provide insights into the possible histogenesis of renal epithelial neoplasms.
肾上皮肿瘤在组织发生、疾病分类及诊断方面存在一些未解决的问题,这些问题可能具有超微结构方面的影响。然而,目前尚无根据最新分类对肾上皮肿瘤进行的全面电子显微镜研究。对55例肾上皮肿瘤(31例透明细胞肾细胞癌、11例乳头状肾细胞癌、5例嫌色肾细胞癌、3例肉瘤样肾细胞癌和5例嗜酸细胞瘤)的超微结构观察结果与其光镜表现进行了对比分析。透明细胞肾细胞癌可见与正常近端小管刷状缘相似的长微绒毛,胞质内富含脂质和糖原。乳头状肾细胞癌可见大小不一的微绒毛,少量胞质脂质,但无糖原。嫌色肾细胞癌可见许多胞质小泡和异常线粒体,微绒毛短而粗,数量稀少。肾嗜酸细胞瘤可见许多线粒体,胞质顶端有少量小泡,微绒毛短而粗,数量稀少。透明细胞肾细胞癌、乳头状肾细胞癌和嫌色肾细胞癌的嗜酸性细胞变体,除胞质内线粒体数量增多外,其超微结构特征与其各自的原型相似。1例肉瘤样透明细胞肾细胞癌显示骨骼肌分化。仅在透明细胞肾细胞癌中发现了两种胞质内含物,即透明小体和类似于潘氏细胞的颗粒(类潘氏细胞颗粒),其具有独特的超微结构特征。当前的电镜研究显示了肾上皮肿瘤独特的超微结构特征。这些发现为相关肿瘤类型的现有分类提供了更多支持,有助于鉴别诊断,并为肾上皮肿瘤的可能组织发生提供了见解。