Adrenal Pheochromocytoma: A Case Report
Milind Pande, Sunita Vagha, Aditi Goyal & Raunak Kotecha · Journal of Pharmaceutical Research International · 2021
Pheochromocytoma is a rare catecholamine secreting tumour originating usually from adrenal medulla and produces signs and symptoms due excessive catecholamine secretion from tumour. A young male patient of 36 yrs age presented with hypertension since 2 yrs, palpitation, profuse s...
Open access
Research Article
10.9734/jpri/2021/v33i64A35757