In 1938, Owen described a malignant renal neoplasm with a peculiar histological pattern. The peculiarity consisted in the tumour cells forming glomerular structures made up of cuboidal cells with clear cytoplasm, indistinct borders and round hyperchromatic nuclei. The glomerular structures had no vascular tufts but showed, at the periphery, a limiting membrane lined by cuboidal cells in one or ...

Primary small cell neuroendocrine carcinoma (SCNEC) is a rare high-grade malignant neoplasm with differentiation derived from the urothelium. Herein, we report case which presented symptomatic anaemia secondary to haematuria, complicated acute kidney injury following obstructive uropathy caused by SCNEC, along discussion of clinical presentation, radiological imaging and pathological findings d...

An interesting case of nonobstructive lower pole hydronephrosis associated with reflux and simulating a neoplasm is presented and discussed. Advanced hydronephrosis localized to one portion of a duplicated kidney in adults may simulate a renal neoplasm on intravenous pyelogram. Upper pole hydronephrosis is a well-described clinical entity and is prominent in the differential diagnosis of renal ...

We present a case of a 52-year-old Caucasian male who underwent a laparoscopic nephrectomy for an atrophic kidney and was found to have two unexpected, synchronous kidney cancers. He had a remote history of testicular cancer complicated by lymphadenopathy and external ureteral compression. Over time, he developed an atrophic left kidney from obstructive uropathy. Years later, due to flank pain ...

The etiology of adenoma of the ampulla of Vater is not well understood. Previous authors reported the association of this neoplasm with polycystic kidney disease of two fraternal sisters. They concluded that these two conditions were somehow related. We describe a case of ampullary adenoma associated with polycystic kidney disease. This presentation raises again the question of a possible link ...

We report a case of a large malignant solitary fibrous kidney tumor. A complete surgical resection of the primary tumor and peritoneal disease was carried out, and a histological examination confirmed the initial diagnosis. We describe and discuss the characteristics of this rare kidney neoplasm.

Nephrolithic non-functioning kidney and malakoplakia are major health problems. Kidney function cannot be fulfilled and also this leads to a high risk of development of urothelial neoplasm. We report herein a case of urothelial carcinoma concomitant with malakoplakia in non-functioning nephrolithic kidneys.

Solitary fibrous tumors are neoplasms of mesenchymal origin that may occur virtually in any body part, most commonly arising from the pleura. Solitary fibrous tumor of the kidney is exceptionally rare, and limited clinical knowledge regarding its behavior makes prognosis of the neoplasm difficult. We report a case of solitary fibrous tumor of the left kidney and describe its clinical, imaging, ...