2014
DOI: 10.14740/jmc1797w
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Mixed Epithelial and Stromal Tumor of the Kidney: A Rare Case Report

Abstract: Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare kidney tumor that is composed of both epithelial and mesenchymal components with solid and cystic architecture. Up to the present, approximately 100 cases have been reported. It was introduced in the World Health Organization 2004 renal tumor classification. Here, we report a 49-year-old female with mixed epithelial and stromal tumor (MEST) in her kidney with no cystic components and no history of hormone use.

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(16 citation statements)
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“…Due to this information it can be considered that hormones are a risk factor for this tumor. The clinical presentation of MEST is similar to typical renal tumor (1,2,(4)(5)6,8,(10)(11)(12). However approximately ¼ of known diagnosed MESTs were asymptomatic.…”
Section: Introductionmentioning
confidence: 82%
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“…Due to this information it can be considered that hormones are a risk factor for this tumor. The clinical presentation of MEST is similar to typical renal tumor (1,2,(4)(5)6,8,(10)(11)(12). However approximately ¼ of known diagnosed MESTs were asymptomatic.…”
Section: Introductionmentioning
confidence: 82%
“…The risk of malignant transformation in a patient with MEST is highly dependent on the individual characteristics of a tumor. A few cases of malignant transformation have been described in the literature, affecting both epithelium or stromal tumor (1)(2)(3)(4)(5)(6)(7)(8)(10)(11)(12), including transformation into sarcoma, rhabdomyosarcoma, chondrosarcoma or papillary renal cell carcinoma. Thus, the differential diagnosis of MEST should include the above malignancies (1)(2)(3)(4)(5)(6)(7)11,12).…”
Section: Discussionmentioning
confidence: 99%
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