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Pheochromocytomas are rare catecholamine secreting neuroendocrine tumors that can cause intracerebral hemorrhage sometimes and can very rarely cause cardiomyopathy simulating hypertrophic obstructive cardiomyopathy. We report a case of combination of these rare clinical complications occurring in a patient with pheochromocytoma. This case illustrates importance of early recognition of classic symptoms of catecholamine excess in young patients with hypertension.doi:10.18203/2349-3933.ijam20211065 fatcat:woszc5eus5cufijdtfksxoeene