Jafri S Z, Freeman J L, Rosenberg B F, Cacciarelli A, Madrazo B L
Department of Diagnostic Radiology, William Beaumont Hospital, Royal Oak, MI 48073.
Urol Radiol. 1991;13(2):94-7. doi: 10.1007/BF02924598.
Rhabdoid tumor of the kidney (RTK) is a rare, highly malignant neoplasm of childhood. The clinical profile of this neoplasm differs from that of Wilms' tumor. We present two cases of RTK. In both our cases, large bulky masses with poorly defined margins and calcifications were demonstrated. The clinical and imaging findings are compared with other childhood renal neoplasms.
肾横纹肌样瘤(RTK)是一种罕见的儿童高度恶性肿瘤。该肿瘤的临床特征与肾母细胞瘤不同。我们报告两例肾横纹肌样瘤。在我们的两个病例中,均显示出边界不清且有钙化的巨大肿块。将临床和影像学表现与其他儿童肾肿瘤进行了比较。