首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Cystic partially differentiated nephroblastoma in an adult: a case imitating the process of normal nephrogenesis along with corresponding WT1 expression
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Cystic partially differentiated nephroblastoma in an adult: a case imitating the process of normal nephrogenesis along with corresponding WT1 expression

机译:成人囊性部分分化肾母细胞瘤:一例模仿正常肾生成过程及相应WT1表达的病例

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Cystic partially differentiated nephroblastoma (CPDN) is extremely rare in adults. Only 2 cases have been documented in the English literature. Herein, we present a third case of CPDN with unique morphological and immunohistochemical features. A 45-year-old man had a multicystic right renal mass, with a maximum diameter of 3 cm on magnetic resonance imaging. Being unable to rule out malignancy, partial nephrectomy was performed. The surgically resected specimen contained a multicystic mass, 3 × 3 × 2.5 cm in size, without an expansile solid nodule. Histopathological examination revealed nephroblastomatous elements without identifiable blastema; transition from cap-mesenchyme-like cells to an immature glomerulus was observed and maturing tubules and a glomerulus were present. Despite the lack of a blastema, the diagnosis of CPDN was the most appropriate. Immunohistochemical WT1 expression imitated the pattern of ongoing normal nephrogenesis. Therefore, we believe that the blastema disappeared because of maturation.
机译:囊性部分分化肾母细胞瘤(CPDN)在成年人中极为罕见。英文文献中仅记录了2个案例。在本文中,我们介绍了第三例CPDN,具有独特的形态学和免疫组化特征。一名45岁的男子患有多囊性右肾肿块,磁共振成像最大直径为3厘米。为了排除恶性肿瘤,进行了部分肾切除术。手术切除的标本包含多囊肿,大小为3×3×2.5 cm,没有膨胀的实性结节。组织病理学检查显示肾母细胞瘤元素,没有可辨认的胚泡。观察到从帽间质样细胞向不成熟的肾小球的过渡,并且存在成熟的肾小管和肾小球。尽管没有胚泡,但诊断CPDN是最合适的。免疫组织化学WT1表达模仿正在进行的正常肾生成的模式。因此,我们认为胚泡由于成熟而消失。

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