6A rare case of cardiac failure due to hypertensive crisis in pheochromocytoma in a 25-year-old young man is presented. In the Emergency Department the patient complained of persisting headache and vomiting; he was distressed but fully alert, his heart rate was 110 b/min and blood pressure 180/ 80 mmHg. Few hours after admission, the clinical course suddenly got worse with signs and symptoms of fatal cardiac shock (dyspnoea, cyanosis, pulmonary oedema, hypocontractility of left ventricle). Autopsy revealed a large tumour of the left adrenal gland. Histological examination confirmed macroscopic suspicion of pheochromocytoma. Catecholamine serum levels were analysed by high pressure liquid chromatography (HPLC) with electrochemical detection....
Pheochromocytoma (Pheo) is an uncommon neoplasm producing blood pressure troubles and it may be undi...
Introduction. Pheochromocytoma is a rare and usually benign catecholamine-secreting tumor with a bro...
This case report describes a patient who presented with severe biventricular cardiac failure and sho...
Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Sympto...
AbstractPheochromocytoma is a rare neuroendocrine tumor with a highly variable clinical presentation...
A 22-year-old man presented to the hospital with progressive shortness of breath, chest discomfort, ...
We report a 42-year-old female who presented with retrosternal pain, dyspnoea and nausea. Electrocar...
Background: Pheochromocytoma is a neuroendocrine tumor that predominantly presents with hypertension...
<p>Pheochromocytoma is a rare tumor in adults, with an estimated annual incidence of 0.8 per 100,000...
Pheochromocytoma, a rare catecholamine-secreting tumor, typically manifests itself with paroxysmal h...
Pheochromocytoma is a rare neuroendocrine tumor arising from the medulla of the adrenal glands, whic...
Pheochromocytoma is unusual catecholamine emit tumor start typically from adrenal medulla and maker ...
Pheochromocytomas are infrequent tumors arised from the chromaphine cells of the adrenal sympathetic...
Pheochromocytomas are infrequent tumors arised from the chromaphine cells of the adrenal sympathetic...
Pheochromocytoma is unusual catecholamine emit tumor start typically from adrenal medulla and maker ...
Pheochromocytoma (Pheo) is an uncommon neoplasm producing blood pressure troubles and it may be undi...
Introduction. Pheochromocytoma is a rare and usually benign catecholamine-secreting tumor with a bro...
This case report describes a patient who presented with severe biventricular cardiac failure and sho...
Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Sympto...
AbstractPheochromocytoma is a rare neuroendocrine tumor with a highly variable clinical presentation...
A 22-year-old man presented to the hospital with progressive shortness of breath, chest discomfort, ...
We report a 42-year-old female who presented with retrosternal pain, dyspnoea and nausea. Electrocar...
Background: Pheochromocytoma is a neuroendocrine tumor that predominantly presents with hypertension...
<p>Pheochromocytoma is a rare tumor in adults, with an estimated annual incidence of 0.8 per 100,000...
Pheochromocytoma, a rare catecholamine-secreting tumor, typically manifests itself with paroxysmal h...
Pheochromocytoma is a rare neuroendocrine tumor arising from the medulla of the adrenal glands, whic...
Pheochromocytoma is unusual catecholamine emit tumor start typically from adrenal medulla and maker ...
Pheochromocytomas are infrequent tumors arised from the chromaphine cells of the adrenal sympathetic...
Pheochromocytomas are infrequent tumors arised from the chromaphine cells of the adrenal sympathetic...
Pheochromocytoma is unusual catecholamine emit tumor start typically from adrenal medulla and maker ...
Pheochromocytoma (Pheo) is an uncommon neoplasm producing blood pressure troubles and it may be undi...
Introduction. Pheochromocytoma is a rare and usually benign catecholamine-secreting tumor with a bro...
This case report describes a patient who presented with severe biventricular cardiac failure and sho...