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Publikováno v:
Rare Tumors, Vol 5, Iss 3, Pp e46-e46 (2013)
Epithelioid angiomyolipomas (EAMLs) are rare mesenchymal tumors whose malignant variant is extremely uncommon and highly aggressive. Treatment strategies include chemoradiation, transcatheter arterial embolization and surgical resection, which has re
Externí odkaz:
https://doaj.org/article/e8f95f7ac53b4fd08c237d9d2b36f4b2