Results 21 to 30 of about 74,479 (241)
Pheochromocytoma with Takotsubo Syndrome and acute heart failure: a case report
Background Pheochromocytoma is a neuroendocrine tumor that can overproduce catecholamines. Heart failure and Takotsubo Syndrome (TTS) caused by excessive catecholamines are uncommon pheochromocytoma complications.
Lin Yang+3 more
doaj +1 more source
ObjectivePheochromocytoma is a rare catecholamine-producing neuroendocrine tumour originating from the chromaffin cells of the adrenal medulla or extra-adrenal paraganglia. However, there are few bibliometric studies on Pheochromocytoma.
Bi-ling Huang+17 more
doaj +1 more source
Pheochromocytomas are catecholamine-secreting tumors derived from chromaffin tissue of the adrenal medulla. Closely related tumors, called extra-adrenal paragangliomas, can arise at extra-adrenal sites. Catecholamine secretion from these tumors is often episodic, causing headache, perspiration, palpitations and hypertension.
Estey, MP+6 more
openaire +3 more sources
Composite pheochromocytoma associated with neurofibromatosis type 1
Introduction Composite pheochromocytoma is a rare tumor, occurring in only 3% of pheochromocytomas. We report a case of composite pheochromocytoma with neurofibromatosis type 1.
Akira Tachibana+5 more
doaj +1 more source
Acute heart failure with incidentally found cystic adrenal mass
Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Symptoms and signs associated with pheochromocytomas are usually intermittent and chronic but can rarely develop into life-threatening crises.
Salman Zahoor Bhat+4 more
doaj +1 more source
Unusual presentation of pheochromocytoma: thirteen years of anxiety requiring psychiatric treatment
Pheochromocytoma is a rare tumor of the adrenal gland. It often presents with the classic triad of headache, palpitations and generalized sweating. Although not described as a typical symptom of pheochromocytoma, anxiety is the fourth most common symptom
Catherine Alguire+4 more
doaj +1 more source
A single cell clonal line which responds reversibly to nerve growth factor (NGF) has been established from a transplantable rat adrenal pheochromocytoma. This line, designated PC12, has a homogeneous and near-diploid chromosome number of 40.
L. Greene, A. Tischler
semanticscholar +1 more source
Epidemiology of Pheochromocytoma and Paraganglioma: Population-based Cohort Study.
OBJECTIVE Despite the significant morbidity and mortality associated with pheochromocytoma and paraganglioma, little is known about their epidemiology.
A. Leung+7 more
semanticscholar +1 more source
Pheochromocytoma with lung metastases is rare in clinics, and the prognosis of metastatic pheochromocytoma is generally poor. In this case, a 57-year-old woman who presented with hypertension and palpitations was diagnosed with left adrenal ...
Hongbing Shi+6 more
doaj +1 more source
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
OBJECTIVE The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). PARTICIPANTS The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), seven experts in the ...
J. Lenders+8 more
semanticscholar +1 more source