We report a patient who presented with two episodes of severe hypertension after intramuscular injection of betamethasone. The first attack was associated with pulmonary edema, while the second attack was associated with high anion gap metabolic acidosis, renal failure, hyperglycemia, and hypokalemia. The attacks led to the diagnosis of pheochromocytoma, which was confirmed by appropriate diagnostic tests. The tumor was excised successfully and the patient is presently asymptomatic. We believe that these episodes were initiated by glucocorticoid injection, an event reported in a few cases. We briefly review potential mechanisms resulted in hypertensive crisis in such patients
Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. ...
Transient or permanent hypertension may result from the inappropriate activation of the sympathetic ...
Introduction We report an unusual case of pheochromocytoma unmasked by anaphylaxis. Clinical case A ...
Abstract Background There are several reports of pheochromocytoma crisis triggered by systemic gluco...
Context. Pheochromocytomas are hormone secreting tumors of the medulla of the adrenal glands found i...
BACKGROUND: Glucocorticoids as diagnostic or therapeutic agents have been reported to carry an incre...
Pheochromocytomas (PCCs) are rare catecholamine-secreting tumors arising from adrenomedullary chroma...
The dramatic presentation of pheochromocytoma in crisis is uncommon and is classically associated wi...
Background: Pheochromocytoma is a neuroendocrine tumor that predominantly presents with hypertension...
The dramatic presentation of pheochromocytoma in crisis is uncommon and is classically associated wi...
Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Sympto...
Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its fre...
In patients with pheochromocytomas it is well known that differentfactors can precipitate an acute p...
KEY CLINICAL MESSAGE: Adrenergic crisis induced by a pheochromocytoma leads to life-threatening cate...
Pheochromocytomas are rare adrenal neoplasms characterized by excess secretion of catecholamines. We...
Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. ...
Transient or permanent hypertension may result from the inappropriate activation of the sympathetic ...
Introduction We report an unusual case of pheochromocytoma unmasked by anaphylaxis. Clinical case A ...
Abstract Background There are several reports of pheochromocytoma crisis triggered by systemic gluco...
Context. Pheochromocytomas are hormone secreting tumors of the medulla of the adrenal glands found i...
BACKGROUND: Glucocorticoids as diagnostic or therapeutic agents have been reported to carry an incre...
Pheochromocytomas (PCCs) are rare catecholamine-secreting tumors arising from adrenomedullary chroma...
The dramatic presentation of pheochromocytoma in crisis is uncommon and is classically associated wi...
Background: Pheochromocytoma is a neuroendocrine tumor that predominantly presents with hypertension...
The dramatic presentation of pheochromocytoma in crisis is uncommon and is classically associated wi...
Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Sympto...
Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its fre...
In patients with pheochromocytomas it is well known that differentfactors can precipitate an acute p...
KEY CLINICAL MESSAGE: Adrenergic crisis induced by a pheochromocytoma leads to life-threatening cate...
Pheochromocytomas are rare adrenal neoplasms characterized by excess secretion of catecholamines. We...
Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. ...
Transient or permanent hypertension may result from the inappropriate activation of the sympathetic ...
Introduction We report an unusual case of pheochromocytoma unmasked by anaphylaxis. Clinical case A ...