Results 251 to 260 of about 82,056 (278)
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Acta Endocrinologica, 1961
ABSTRACT Two new cases of metastatic malignant pheochromocytoma are presented. An increased excretion of norepinephrine was demonstrated in both. The literature on malignant pheochromocytoma has been critically evaluated.
G, PALMIERI, D, IKKOS, R, LUFT
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ABSTRACT Two new cases of metastatic malignant pheochromocytoma are presented. An increased excretion of norepinephrine was demonstrated in both. The literature on malignant pheochromocytoma has been critically evaluated.
G, PALMIERI, D, IKKOS, R, LUFT
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Intrapericardial pheochromocytoma
The Annals of Thoracic Surgery, 1991In a 34-year-old man with hypertension and increased urinary catecholamine excretion for 12 years, an m-[131I]iodobenzylguanidine scan and chest computed tomography located an intrapericardial pheochromocytoma in the left atrium. The tumor was excised through a left thoracotomy with cardiopulmonary bypass and circulatory arrest.
C H, Chang +6 more
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The Annals of Thoracic Surgery, 2001
Primary pheochromocytomas of the heart are extremely uncommon. In this report, we present the case of a patient with primary cardiac pheochromocytoma arising from the interatrial septum. Metaiodobenzylguanidine-scintigraphy was negative and diagnosis was confirmed by a positive octreotide scintiscan.
J P, Meunier +4 more
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Primary pheochromocytomas of the heart are extremely uncommon. In this report, we present the case of a patient with primary cardiac pheochromocytoma arising from the interatrial septum. Metaiodobenzylguanidine-scintigraphy was negative and diagnosis was confirmed by a positive octreotide scintiscan.
J P, Meunier +4 more
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International Journal of Surgical Pathology, 2014
Introduction. Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare neuroendocrine tumors with an estimated occurrence of 2 to 5 patients per million per year and an incidence of about 1 per 100 000 in the general population. These tumors may arise sporadically or be associated to various syndromes, namely multiple endocrine neoplasia type 2 ...
Pedro, Santos +2 more
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Introduction. Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare neuroendocrine tumors with an estimated occurrence of 2 to 5 patients per million per year and an incidence of about 1 per 100 000 in the general population. These tumors may arise sporadically or be associated to various syndromes, namely multiple endocrine neoplasia type 2 ...
Pedro, Santos +2 more
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Cardiology in Review, 1983
Pheochromocytomas cause the most dramatic, life-threatening crises in all of endocrinology. Pheochromocytoma is an explosive clinical syndrome characterized by severe hypertension associated with cardiac complications, hypotension, or even shock and sudden death. The key to diagnosing pheochromocytoma is to suspect it, then confirm it.
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Pheochromocytomas cause the most dramatic, life-threatening crises in all of endocrinology. Pheochromocytoma is an explosive clinical syndrome characterized by severe hypertension associated with cardiac complications, hypotension, or even shock and sudden death. The key to diagnosing pheochromocytoma is to suspect it, then confirm it.
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