Results 21 to 30 of about 74,479 (241)

Pheochromocytoma with Takotsubo Syndrome and acute heart failure: a case report

open access: yesWorld Journal of Surgical Oncology, 2022
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

Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years

open access: yesFrontiers in Endocrinology, 2023
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

Pheochromocytoma [PDF]

open access: yesClinical Chemistry, 2013
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

open access: yesIJU Case Reports, 2023
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

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2023
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

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2018
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

Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor.

open access: yesProceedings of the National Academy of Sciences of the United States of America, 1976
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.

open access: yesEuropean Journal of Endocrinology, 2020
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

Case Report: Successful Control of Pulmonary Metastatic Pheochromocytoma With Iodine-125 Seed Implantation

open access: yesFrontiers in Endocrinology, 2021
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.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2014
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

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