Multilocular cystic renal tumor |
Bimodal age distribution, young boys and middle-aged women |
Large, multiseptated, cystic mass separated by thick, enhancing septations |
Renal medullary carcinoma |
Predominance in black patients with sickle cell trait |
Aggressive, infiltrating neoplasm arising from the medulla |
Collecting duct carcinoma |
Aggressive neoplasm arising from the medulla |
Metanephric adenoma |
Produces erythropoietin and is associated with polycythemia in 12% of cases |
Benign neoplasm related histologically to Wilms tumor |
Leiomyoma |
Commonly found in women in the 2nd to 5th decade of life |
Hypervascular |
Benign |
Hemangioma |
Demonstrates early intense enhancement on the arterial phase that persists on the delayed phase |
Hyperintense on T2-weighted MR images |
Lymphangioma |
Well-defined uni-or multiloculated mass arising from the renal sinus or perinephric space; locules do not enhance |
Communicating cysts with lymphoid cells in their septa |
Sarcoma |
Different histologic subtypes: leiomyosarcoma, angiosarcoma, rhabdomyosarcoma, etc. |
Nonspecific imaging characteristics |
Renomedullary interstitial tumor |
Benign tumors arising from renomedullary interstitial cells |
Commonly found on autopsies as small lesions, but clinically are rare and not seen |
Carcinoid |
Neuroendocrine tumor that can manifest with carcinoid syndrome on liver metastasis |
Somatostatin receptor scintigraphy can aid in staging, but not often in locating the renal tumor |
Small cell carcinoma |
Resembles its counterparts arising from the trachea-bronchial tree |
Aggressive behavior |
Juxtaglomerular apparatus tumor |
May produce elevated renin, associated with hypertension |