Gundes, EbubekirAksoy, FarukTasci, Halil IbrahimYilmaz, Osman2024-02-232024-02-2320161305-93191305-9327https://doi.org/10.5350/BTDMJB201612109https://hdl.handle.net/20.500.12452/16877Paraganglioma (PG), also known as extra-adrenal pheochromocytoma, is a rare neuroectodermal tumor. The incidence of extra-adrenal paraganglioma is between 00.1-0.1%. Paragangliomas originating from the retroperitoneum are generally functional. 40-50% of them are malignant and they generally have a slow progression. Surgical resection and radiotherapy are the preferred methods for the local treatment of these tumors. A case with a tumor localized in the retroperitoneal space that was totally resected by surgical method was evaluated.trinfo:eu-repo/semantics/closedAccessParagangliomaExtra-AdrenalRetroperitoneal SpaceArticle12151532-s2.0-84964720125Q4WOS:00037515620000910.5350/BTDMJB201612109