Arch Esp Urol 2017 Sep;70(7):670-674
Departamento de Urología Oncológica. Instituto Nacional de Enfermedades Neoplásicas. Lima-Perú.
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J Pediatr Surg 2001 Dec;36(12):1796-801
Departments of Pediatric Surgery and Pediatric Oncology, Hacettepe University Medical Faculty, Ankara, Turkey.
Purpose: The aim of this study was to present an updated picture of surgical management of pediatric testicular tumors based on our 30 years' experience, which consisted of one of the largest noncollected series treated in a single medical center.
Methods: Records of children who were treated for testicular tumor in our unit from 1970 to 1999, inclusive, were reviewed retrospectively. Information recorded for each patient included age, sex, past medical history, clinical characteristics, diagnostic procedures, treatment methods, histopathologic findings, and outcome. Read More
Urology 2009 May 2;73(5):1163.e9-11. Epub 2008 Jul 2.
Department of Surgery, Division of Urology, Tri-Service General Hospital, Taipei, Taiwan.
Ipsilateral multiple synchronous primary renal neoplasms is an uncommon presentation, and only a few cases have been reported in published studies. We report the case of a 57-year-old woman with acute pyelonephritis as the initial presentation, in whom conservative treatment had no effect. Surgical intervention revealed the presence of concomitant renal cell carcinoma, collecting duct carcinoma, and urothelial carcinoma (transitional cell carcinoma) of the kidney. Read More
Actas Urol Esp 1997 Mar;21(3):260-3
Servicio de Urología, Hospital Universitario de Canarias, Tenerife.
Until very recently, bilateral renal cell carcinoma was considered to be of very poor prognosis due to the poor results obtained with either radiotherapy or chemotherapy, which were completely ineffective in this type of tumours. In 1952, Krumbach performed the first radical nephrectomy and partial nephrectomy to a patient with bilateral synchronic renal cell carcinoma. This aggressive approach to bilateral renal cell carcinoma definitely changed the prognosis of these patients. Read More
West Afr J Med 2011 Nov-Dec;30(6):447-52
Callaghan Brendon Costello, Madhuri Deolekker, North Manchester General Hospital,Departments of Urology and Pathology Delaunays Road, Crumpsall, Manchester, M8 5RB, United Kingdom.
Background: Paratesticular liposarcomas are uncommon and in view of this most practitioners would be unfamiliar with the diagnosis and management.
Objective: To report a case of paratesticular liposarcoma, a rare tumour and to review the literature on paratesticular liposarcoma.
Methods And Results: A 77-years old man with paratesticular liposarcoma originating from the left spermatic cord is reported. Read More