Results 11 to 20 of about 51,442 (242)

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

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 [PDF]

open access: yesAnesthesiology, 1978
Pheochromocytoma, a relatively rare (<0.05% of hypertensives), catecholamine‐secreting tumor, is almost always lethal unless recognized and appropriately treated. Clinical and biochemical manifestations are mainly caused by excess circulating catecholamines and hypertension.
William M, Manger, Ray W, Gifford
openaire   +2 more sources

A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?

open access: yesInternational Journal of Endocrinology, 2018
Pheochromocytoma is very rare at a pediatric age, and when it is present, the probability of a causative genetic mutation is high. Due to high costs of genetic surveys and an increasing number of genes associated with pheochromocytoma, a sequential ...
Bernardo Dias Pereira   +6 more
doaj   +1 more source

The importance of pheochromocytoma case detection in patients with neurofibromatosis type 1: A case report and review of literature

open access: yesSAGE Open Medical Case Reports, 2017
Neurofibromatosis type 1 is a complex, multi-system genetic disorder that is associated with an increased prevalence of pheochromocytoma and paraganglioma compared to the general population, 1.0%–5.7% versus 0.2%–0.6%, respectively.
Joshua M Tate   +2 more
doaj   +1 more source

Pheochromocytomas and paragangliomas [PDF]

open access: yesCurrent Opinion in Pediatrics, 2021
Purpose of review Great progress has been made in understanding the genetic and molecular basis of pheochromocytoma and paragangliomas (PPGLs). This review highlights the new standards in the diagnosis and management of pediatric PPGLs. Recent findings The vast majority of pediatric
Yen, Kevin, Lodish, Maya
openaire   +3 more sources

Pulsed Electromagnetic Fields: A Novel Attractive Therapeutic Opportunity for Neuroprotection After Acute Cerebral Ischemia

open access: yesNeuromodulation: Technology at the Neural Interface, EarlyView., 2021
Abstract Objectives Acute cerebral ischemia is characterized by several pathological processes evolving during time, which contribute to the final tissue damage. Secondary processes, such as prolonged inflammatory response, impaired mitochondrial function and oxidative stress, are responsible for the progression of brain injury to the peri‐infarct area,
Fioravante Capone   +8 more
wiley   +1 more source

Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C

open access: yesJournal of Pediatric Research, 2018
Pheochromocytoma is a rare disease that is characterized by the increased production and secretion of catecholamines from the adrenal medulla. The disease is autosomal dominant, and frequently sporadic and unilateral. Pheochromocytoma, which is diagnosed
Sezer Acar   +9 more
doaj   +1 more source

Silent Hypertensive Crisis in an Adolescent: First Case Report of Pediatric Pheochromocytoma from Indonesia

open access: yesGlobal Pediatric Health, 2021
Secondary hypertension in children, to the rare extent, can be caused by endocrine factors such as pheochromocytoma, an adrenal tumor that secretes catecholamine. Only a few cases have been reported in the past 3 decades.
Cahyani Gita Ambarsari   +6 more
doaj   +1 more source

PHEOCHROMOCYTOMA

open access: bronzeSouthern Medical Journal, 1958
Koji Ochiai   +7 more
openalex   +4 more sources

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