Pheochromocytoma is a rare tumor, usually benign, potentially lethal in case of crisis with
acute release of catecholamines. The heart is a target and the clinical presentation can …

Pheochromocytoma is a relatively rare catecholamine-secreting tumor (0.1 to 0.8% of
hypertensives). It has a large spectrum of clinical and biochemical manifestations. The …

Pheochromocytoma, a relatively rare (0.1-0.8% of hypertensives), catecholamine-secreting
tumor, is almost always lethal unless recognised and appropriately treated. Histological …

Pheochromocytoma is a tumor originating from chromaffin tissue. It commonly presents with
symptoms and signs of catecholamine excess, such as hypertension, tachycardia, headache …

Pheochromocytoma is a rare neuroendocrine tumor characterized by overproduction of
catecholamines. The overproduction of catecholamines leads to cardiac remodeling which …

Pheochromocytoma is a rare, catecholamine-secreting tumor. The classic symptoms are
headache, diaphoresis, and tachycardia with paroxysmal hypertension. Other less common …

Cardiac involvement in pheochromocytoma is rare but may be associated with serious
clinical deterioration. A 70-year-old woman arrived at our Emergency Department because …

Catecholamine-induced cardiomyopathy is a rarecomplication of pheocromocytoma. We
present acase of pheocromocytoma that developed preoperativeheart failure. Left …

Introduction Pheochromocytomas are infrequent tumors arised from the chromaphine cells
of the adrenal sympathetic system. The excess of circulating catecholamines may lead to …

Pheochromocytoma is a neuroendocrine tumor, characterized by an excess of
catecholamine production, which results in paroxysmal or sustained hypertension, even …