Abstract:Background: Pheochromocytoma (PCC) and paraganglioma (PGL) are rare tumors occurring in the adrenal medulla and extra-adrenal tissues, respectively. The clinicopathological features have not been fully elucidated, especially in Asian cohorts.
Methods:We retrospectively reviewed 65 patients with PCC/PGL between 1983 and 2020. Patient characteristics and clinical outcomes (overall survival [OS] and relapsefree survival [RFS]) were analyzed based on the medical records. Morphological assessment and immunostaining… Show more
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