Results 81 to 90 of about 74,479 (241)
Spontaneous adrenal pheochromocytoma rupture complicated by intraperitoneal hemorrhage and shock
MEN2A is a hereditary syndrome characterized by medullary thyroid carcinoma, hyperparathyroidism, and pheochromocytoma. Classically patients with a pheochromocytoma initially present with the triad of paroxysmal headaches, palpitations, and diaphoresis ...
Kwasnik Edward+4 more
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Extracorporeal membrane oxygenation for pheochromocytoma-induced cardiogenic shock
BackgroundPheochromocytoma, a rare catecholamine-producing tumor, might provoke stress-induced Takotsubo-like cardiomyopathy and severe cardiogenic shock.
G. Hékimian+12 more
semanticscholar +1 more source
Cushing's syndrome due to adrenocorticotropic hormone-secreting pheochromocytoma
Adrenocorticotropic hormone (ACTH) producing pheochromocytoma is the rare cause of Cushing's syndrome (CS). Herein, we present a 53-year-old female patient with ectopic ACTH-dependent Cushing's syndrome due to pheochromocytoma.
G V Chanukya, Manoj Mengade, Babu Reddy
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MANAGEMENT OF ENDOCRINE DISEASE: Outcome of adrenal sparing surgery in heritable pheochromocytoma.
The management of hereditary pheochromocytoma has drastically evolved in the last 20 years. Bilateral pheochromocytoma does not increase mortality in MEN2 or von Hippel-Lindau (VHL) mutation carriers who are followed regularly, but these mutations induce
F. Castinetti+8 more
semanticscholar +1 more source
A Narrative Review of Pheochromocytoma in VHL
This systematic review aims to investigate the clinical presentation, diagnostic methods, and management strategies for pheochromocytoma in patients with von Hippel-Lindau (VHL) disease, an autosomal dominant disorder that predisposes individuals to the
Danilo Coco, Silvana Leanza
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Anesthetic Management of Pheochromocytoma [PDF]
J. Richard Crout, Burnett R. Brown
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Cardiac Arrhythmias Associated with Succinylcholine in a Patient with Pheochromocytoma [PDF]
Theodore K. Stoner, KARL F. URBACH
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