A case report of aggressive mixed epithelial and stromal tumor of the kidney with malignant transformation

被引：0

作者：

Djafari, Anahita Ansari ^{[1
]}

Rahnama, Hossein ^{[2
]}

Javanmard, Babak ^{[2
]}

Hojjati, Seyyed Ali ^{[2
]}

Salarinejad, Sareh ^{[3
]}

机构：

[1] Shahid Beheshti Univ Med Sci, Shohada Etajrish Hosp, Laser Applicat Med Sci Res Ctr, Tehran, Iran

[2] Shahid Beheshti Univ Med Sci, Shohada E Tajrish Hosp, Dept Urol, Tehran, Iran

[3] Shahid Beheshti Univ Med Sci, Shohada E Tajrish Hosp, Fac Med, Dept Pathol, Tehran, Iran

来源：

UROLOGY CASE REPORTS | 2024年 / 53卷

关键词：

Kidney; Mixed epithelial and stromal tumor; Renal mass; Sarcomatoid component;

D O I：

10.1016/j.eucr.2024.102689

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare benign kidney tumor. In rare cases, malignant transformation, such as sarcomatoid features indicates poor clinical outcomes. In this study, we will describe a 45 years old man with a diagnosis of MESTK with malignant transformation of the sarcomatoid component, after right radical nephrectomy. The patient underwent chemotherapy with adriamycin, ifosfamide, and granulocyte-colony stimulating factor (G-CSF). The radiological characteristics of MESTK can pose diagnostic challenges due to its non-unique radiological appearance. The presence of sarcomatoid transformation is a hallmark feature of malignant MESTK which can be very aggressive.

引用

页数：3

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