{"id":13360,"date":"2024-08-23T00:52:49","date_gmt":"2024-08-22T22:52:49","guid":{"rendered":"https:\/\/valintermed.com\/?p=13360"},"modified":"2024-08-23T00:52:49","modified_gmt":"2024-08-22T22:52:49","slug":"opuhol-vilmsa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/vilmsa-tumor\/","title":{"rendered":"Wilms tumor"},"content":{"rendered":"
<\/div>\n

Wilms tumor, or nephroblastoma, is a malignant tumor of the kidneys, mainly detected in children. This disease is well known for its rapidly progressive course and is usually diagnosed between the ages of 2 and 5. The tumor arises from immature kidney cells and can be associated with various developmental anomalies. In the early stages, the tumor may be asymptomatic, but as it grows in size, it can manifest itself through an enlarged abdomen, pain in the kidney area, as well as various systemic symptoms, such as anemia and loss of appetite. Despite its aggressive characteristics, high patient survival is achieved thanks to modern diagnostic and treatment methods, which makes Wilms tumor a relevant topic in pediatric oncology.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n