Results 11 to 20 of about 45,090 (245)
Pediatrics In Review, 2011 The book is divided into six sections. The first three sections focus on the pathophysiology of the disease, showing anatomo- and histopathological aspects, experimental models and signaling pathways and programmed cell death related to pheochromocytoma.
Sadiqa, Edmonds +2 more
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Endocrine Regulations, 2019 Abstract Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary syndrome. A considerable number of pheochromocytomas carry germline or somatic gene mutations, which are inherited in the autosomal dominant way. All patients should undergo genetic testing.
Farrugia Frederick-Anthony +1 more
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Anesthesiology, 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
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Unusual presentation of pheochromocytoma: thirteen years of anxiety requiring psychiatric treatment
Endocrinology, 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
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Acute heart failure with incidentally found cystic adrenal mass
Endocrinology, 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
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Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease. [PDF]
, 1996 Inherited pheochromocytomas are often part of familial syndromes, especially multiple endocrine neoplasia type 2 (MEN 2), retinal cerebellar hemangioblastomatosis [von Hippel-Lindau (vHL) disease] or neurofibromatosis type 1.
Crossey, P.A. +7 more
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A Case of Multiple Organ Failure (MOF) Caused by an Adrenal Pheochromocytoma that Ruptured Spontaneously [PDF]
, 2007 We report a case of an adrenal pheochromocytoma that ruptured spontaneously and caused multiple organ failure (MOF). Spontaneous rupture of pheochromocytoma is extremely rare, but it can be lethal because of dramatic changes in the circulation. A 44-year-
中山, 淳 +5 more
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Is It a Pheochromocytoma? [PDF]
The Journal of Clinical Hypertension, 2007 The patient is a 44‐year‐old man with a 4‐year history of intermittently elevated blood pressure (BP) controlled by diet and exercise. Three months before evaluation he described daily “spikes” of BP with sharp unilateral headaches. He was seen in the emergency department with a BP of 212/106 mm Hg and was started on hydrochlorothiazide 25 mg daily ...
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Frontiers 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
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Neuromodulation: 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