Results 201 to 210 of about 45,090 (245)
Some of the next articles are maybe not open access.
Endocrinology and Metabolism Clinics of North America, 1994
None of the endocrine causes for hypertension is more fascinating and challenging for the clinician than pheochromocytoma. Its protean manifestations can make diagnosis difficult, yet its sinister prognostic implications demand prompt recognition and expert management.
R W, Gifford, W M, Manger, E L, Bravo
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None of the endocrine causes for hypertension is more fascinating and challenging for the clinician than pheochromocytoma. Its protean manifestations can make diagnosis difficult, yet its sinister prognostic implications demand prompt recognition and expert management.
R W, Gifford, W M, Manger, E L, Bravo
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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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EVOLUTION OF A PHEOCHROMOCYTOMA
Endocrine Practice, 2006To present a case that demonstrates the evolution of a pheochromocytoma over a several-year period and to emphasize the importance of a thorough work-up for pheochromocytoma in patients with neurofibromatosis type 1 (NF1) and hypertension.We review the long-term clinical, biochemical, and imaging findings in a man with a complex medical history of ...
Steven B, Magill +4 more
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The Annals of Thoracic Surgery, 1986
A patient with a pheochromocytoma involving the posterior wall of the left ventricle and the coronary sinus is reported. Complete surgical removal of the tumor was possible, although it caused a perioperative myocardial infarction. The literature regarding cardiac pheochromocytoma is reviewed.
T E, David +4 more
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A patient with a pheochromocytoma involving the posterior wall of the left ventricle and the coronary sinus is reported. Complete surgical removal of the tumor was possible, although it caused a perioperative myocardial infarction. The literature regarding cardiac pheochromocytoma is reviewed.
T E, David +4 more
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Pheochromocytoma of the bladder
JAAPA, 2017ABSTRACT Pheochromocytoma is a rare catecholamine-secreting tumor. Unless recognized and treated appropriately it can be lethal. Common symptoms include sustained or paroxysmal hypertension associated with headaches, sweating, or palpitations.
Paige, Williams +2 more
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PHEOCHROMOCYTOMA AND PREGNANCY
Annals of Internal Medicine, 1957Excerpt The diagnosis of pheochromocytoma is being made with greater frequency since more reliable tests for its recognition have come into more or less widespread use.
I L, STUTZ +4 more
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The American Journal of Cardiology, 2000
This is a presentation of a unique case of cardiac pheochromocytoma during pregnancy. The case is significant because pheochromocytoma is a difficult diagnosis and its rarity during pregnancy may lead to this important diagnosis being overlooked, even though treatment is specific and highly successful.
T G, Pickering +3 more
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This is a presentation of a unique case of cardiac pheochromocytoma during pregnancy. The case is significant because pheochromocytoma is a difficult diagnosis and its rarity during pregnancy may lead to this important diagnosis being overlooked, even though treatment is specific and highly successful.
T G, Pickering +3 more
openaire +2 more sources