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Juxtaglomerular cell tumor of the kidney: a clinicopathological analysis of five cases 预览 被引量:1
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作者 任国平 余心如 +3 位作者 黎永祥 史时芳 王丽君 叶惠惠 《中华医学杂志:英文版》 SCIE CAS CSCD 2003年第11期 1789-1792,共4页
Juxtaglomerular cell tumor (JGCT) is a kind of rare renal neoplasm that was first described by Robertson in 1967.1 This tumor typically is found in young adults, and patients usually have hypertension, hyperaldosteron... Juxtaglomerular cell tumor (JGCT) is a kind of rare renal neoplasm that was first described by Robertson in 1967.1 This tumor typically is found in young adults, and patients usually have hypertension, hyperaldosteronism and hypokalemia secondary to tumor renin secretion .1-8 To our knowledge, only about 70 cases have been reported including no more than 8 cases in China. Because of its rarity, the clinicopathological features of the tumor have not been clearly established. In this article, 5 cases of JGCT were reported, in order to give a better understanding of its morphological and immunohistochemical profiles. In addition, the immunophenotypical findings of JGCT were compared with 5 cutaneous glomus tumors and 5 hemangiopericytomas, which shared morphological features with JGCT. 展开更多
关键词 肾小球细胞肿瘤 临床病理学 超微结构 诊断 症状
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