| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8807134 | Annales de Pathologie | 2017 | 5 Pages | 
Abstract
												We report the case of a large tumor in the left kidney with necrotic and hemorrhagic features in a 7-month-old child, which was clinically and radiologically suggestive of a nephroblastoma. The tumor was a nodular mass measuring 8 cm in diameter occupying two thirds of the kidney and presenting areas of necrosis and hemorrhage. No capsular rupture or renal sinus infiltration were found. Adjacent renal parenchyma appeared mascroscopically normal. Histologically, the tumor showed a strictly tubulopapillary architectural pattern with numerous psammomas. The initial hypothesis was a purely epithelial nephroblastoma. However, this hypothesis was rejected due to some immunohistochemical and histological characteristics and the final diagnosis was a metanephric adenoma. Metanephric adenoma is an exceptionally rare benign renal tumor in children. However, pathologists need to keep it in mind because simple surgical excision is curative.
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											Authors
												Anne-Sophie Bidaut, Sarah Bouchard, Yvan Samson, Françoise Rypens, Natalie Patey, Dorothée DalSoglio, 
											