Mixed epithelial and stromal tumor of the kidney: a rare case report and review of the literatures.

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-08-15 DOI:10.14740/jmc1797w
Cheng Yang, Jianzhong Wang, Hexi Du, Mingwei Chen, Xia Zhu, Jun Zhou, Z. Hao, Haoqiang Shi, Li Zhang, C. Liang
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引用次数: 3

Abstract

Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare complex renal neoplasm composed of a mixture of cystic and solid components. Until date only few cases of MESTK have been reported. We present here a rare case of MESTK that was diagnosed in a 56-year-old female. The patients were referred to our hospital due to a mass on the right kidney identified incidentally in a routine physical examination. A pre-operative diagnosis of cystic renal cell carcinoma was made and a right radical nephrectomy was carried out. Macroscopically, a cystic tumor was noticed in the upper portion of the right kidney. Various-sized cysts accompanied by multiple cysts and few solid areas were observed. Immunohistochemically, various epithelial markers as well as stromal markers were identified. Taken together with all the immunohistochemical results and morphological pattern of the tumor, a diagnosis of MESTK was made. MESTK is relatively rare and generally benign. However, it is difficult to distinguish between benign or malignant tumors according to the current radiological method. Therefore a complete resection of the tumor by partial or radical nephrectomy is suggested.
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肾上皮和间质混合瘤:罕见病例报告及文献复习。
肾脏混合性上皮和间质瘤(mesk)是一种罕见的由囊性和实性成分混合组成的复杂肾脏肿瘤。迄今为止,仅报告了几例MESTK病例。我们在此报告一例罕见的MESTK病例,诊断为56岁女性。患者因在常规体检中偶然发现右肾肿块而转诊至我院。术前诊断为囊性肾细胞癌,行右侧根治性肾切除术。镜下可见右肾上部一囊性肿瘤。大小不一的囊肿伴多发囊肿,实心区少见。免疫组织化学鉴定了各种上皮标志物和基质标志物。结合所有免疫组化结果和肿瘤的形态学特征,诊断为MESTK。MESTK相对罕见,通常为良性。然而,根据目前的放射学方法,很难区分良性或恶性肿瘤。因此,建议通过部分或根治性肾切除术来完全切除肿瘤。
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