Pheochromocytoma (Ph) is a rare catecholamine-secreting neuroendocrine tumour that arises from the chromaffin cells of the adrenal medulla. Ph usually presents with symptoms including paroxysmal headache, sweating, palpitations, and hypertension.

A case of pheochromocytoma with negative MIBG scintigraphy, PET-CT and genetic tests (VHL included) and a rare case of post-operative erectile dysfunction / Defeudis, G.; Fioriti, E.; Palermo, A.; Tuccinardi, D.; Minucci, A.; Capoluongo, Ettore Domenico; Pozzilli, P.; Manfrini, S.. - In: HORMONES. - ISSN 1109-3099. - 17:2(2018), pp. 279-284. [10.1007/s42000-018-0037-1]

A case of pheochromocytoma with negative MIBG scintigraphy, PET-CT and genetic tests (VHL included) and a rare case of post-operative erectile dysfunction

Capoluongo;
2018

Abstract

Pheochromocytoma (Ph) is a rare catecholamine-secreting neuroendocrine tumour that arises from the chromaffin cells of the adrenal medulla. Ph usually presents with symptoms including paroxysmal headache, sweating, palpitations, and hypertension.
2018
A case of pheochromocytoma with negative MIBG scintigraphy, PET-CT and genetic tests (VHL included) and a rare case of post-operative erectile dysfunction / Defeudis, G.; Fioriti, E.; Palermo, A.; Tuccinardi, D.; Minucci, A.; Capoluongo, Ettore Domenico; Pozzilli, P.; Manfrini, S.. - In: HORMONES. - ISSN 1109-3099. - 17:2(2018), pp. 279-284. [10.1007/s42000-018-0037-1]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/779611
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