A 17-year-old male with symptoms of headache and diaphoresis presented to the emergency department. He had eight months of noted hypertension attributed to medications. On arrival his blood pressure was 229/117mmHg, and he was ill-appearing. His blood pressure was managed aggressively, and he was diagnosed with extra-adrenal pheochromocytoma by computed tomography. He eventually underwent resection of the mass. Children with severe, symptomatic hypertension should be evaluated for pheochromocytoma. Although rare, it is curable. Failure to diagnose carries a high risk of morbidity and mortality. [West J Emerg Med. 2011;12(2):258-261.
Pheochromocytomas are rare adrenal neoplasms characterized by excess secretion of catecholamines. We...
There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is...
Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its fre...
A 17-year-old male with symptoms of headache and diaphoresis presented to the emergency department. ...
A 17-year-old male with symptoms of headache and diaphoresis presented to the emergency department. ...
AbstractPheochromocytoma, (PCC) is a sympathetic paraganglioma of chromaffin cell origin. Individual...
Report of a case of sustained arterial hypertension due to an adrenal medullary tumor, excision of w...
*** When persistent hypertension in adolescents has a rare endocrine etiology: report of two cases ...
Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. ...
AbstractA 15-month-old boy was diagnosed with malignant hypertension caused by a catecholamine excre...
Exta-adrenal pheochromocytomas are rare tumors that arise from extra-adrenal chromaffin cells of the...
Exta-adrenal pheochromocytomas are rare tumors that arise from extra-adrenal chromaffin cells of the...
Fourteen children (10 boys and 4 girls, aged 8 to 17 years) had 20 pheochromocytomas treated over a ...
Objective: Pheochromocytoma is a neoplosia of chromaffin cells that is very rare in children. Its si...
Background and Objective: Less than 1% of pheochromocytoma account for hypertensive vascular disease...
Pheochromocytomas are rare adrenal neoplasms characterized by excess secretion of catecholamines. We...
There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is...
Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its fre...
A 17-year-old male with symptoms of headache and diaphoresis presented to the emergency department. ...
A 17-year-old male with symptoms of headache and diaphoresis presented to the emergency department. ...
AbstractPheochromocytoma, (PCC) is a sympathetic paraganglioma of chromaffin cell origin. Individual...
Report of a case of sustained arterial hypertension due to an adrenal medullary tumor, excision of w...
*** When persistent hypertension in adolescents has a rare endocrine etiology: report of two cases ...
Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. ...
AbstractA 15-month-old boy was diagnosed with malignant hypertension caused by a catecholamine excre...
Exta-adrenal pheochromocytomas are rare tumors that arise from extra-adrenal chromaffin cells of the...
Exta-adrenal pheochromocytomas are rare tumors that arise from extra-adrenal chromaffin cells of the...
Fourteen children (10 boys and 4 girls, aged 8 to 17 years) had 20 pheochromocytomas treated over a ...
Objective: Pheochromocytoma is a neoplosia of chromaffin cells that is very rare in children. Its si...
Background and Objective: Less than 1% of pheochromocytoma account for hypertensive vascular disease...
Pheochromocytomas are rare adrenal neoplasms characterized by excess secretion of catecholamines. We...
There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is...
Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its fre...