Ureteric extension of Wilms' tumour: A case report
نویسندگان
چکیده
منابع مشابه
Adult Wilms' tumour: a case report with review of literature
BACKGROUND Wilms' tumor is the commonest primary malignant renal tumor in childhood. Rarely, it may present in the adult age group. CASE PRESENTATION We report a 48-year-old male presenting with flank pain and haematuria. Abdominal ultrasound revealed a right renal mass measuring 11 x 10 cms, and a clinical diagnosis of renal cell carcinoma was made. Nephrectomy was performed, and a final dia...
متن کاملAdult Wilms’ Tumour: Case Report and Review of Literature
Wilms' tumour (nephroblastoma) is the most common renal tumour in children. Wilms' tumour in adults is extremely rare and has a poorer prognosis than paediatric Wilms' tumour. It is difficult to differentiate adult Wilms' tumour from renal cell carcinoma based on radiological findings alone. The diagnosis in adults is often serendipitous following nephrectomy for presumed renal cell carcinoma. ...
متن کاملWilms' tumour--a case of disrupted development.
Wilms' tumour is a paediatric kidney malignancy that arises through aberrant differentiation of nephric stem cells. We are studying the role of one Wilms' tumour predisposition gene, WT1. This is a tumour suppressor gene whose function is required for normal development of the genitourinary system. WT1 encodes a putative transcriptional repressor of the zinc finger family. Here we discuss how o...
متن کاملExtension of Retropiretoneal Neuroblastoma to Spinal Canal: A Case Report
Neuroblastoma is a nervous system malignancy. The extension of intra-abdominal neuroblastoma to the spinal canal is a rare condition. In this case report, we present a patient with monoplegia and a huge intra-abdominal mass with intra spinal extension and cord compression.
متن کاملAdult Wilms Tumor with Intracaval and Intracardiac Extension: Report of a Case and Review of Literature
Wilms tumor (WT) occurs infrequently in adults. Even rarer is adult WT with extension by direct intravascular spread into the right side of the heart. The present report describes a partially differentiated WT with intracaval and intracardiac extension in a 54-year-old man. The morphologic and immunohistochemical findings confirmed the diagnosis.
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ژورنال
عنوان ژورنال: Journal of Pediatric Urology
سال: 2013
ISSN: 1477-5131
DOI: 10.1016/j.jpurol.2012.03.018