{"id":12777,"date":"2024-10-11T16:00:14","date_gmt":"2024-10-11T14:00:14","guid":{"rendered":"https:\/\/valintermed.com\/?p=12777"},"modified":"2024-10-11T16:00:14","modified_gmt":"2024-10-11T14:00:14","slug":"rabdoidnaya-opuhol","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/rabidoid-tumor\/","title":{"rendered":"Rhabdoid tumor"},"content":{"rendered":"
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Rhabdomyosarcoma is a malignant neoplasm originating from the sympathetic nervous system and the chest, and also acting as an aggressive tumor process in soft tissues. The disease is associated with changes in the myogenic lineage and has various molecular subtypes, which makes it difficult to diagnose and treat. Rhabdoid tumors often occur in children and adolescents, but can also occur in adults. These tumors are characterized by an aggressive course, a high level of metastasis and a poor prognosis, which emphasizes the need for early diagnosis and effective treatment.<\/p>\n

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