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Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report [PDF]
Annals of Noninvasive ElectrocardiologyPheochromocytoma, a type of neuroendocrine tumor, can cause numerous symptoms and signs similar to those of other clinical conditions, with the classic triad being palpitations, headache, and diaphoresis.
Gui‐yang Li +3 more
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The American Journal of Surgery, 1962 Since pheochromocytomas result in a curable form of hypertension, there should be an awareness of its diagnostic features. These include the following: paroxysmal hypertension, paroxysmal vasomotor phenomena, hypermetabolism with loss of weight or elevation of the basal metabolic rate, and “diabetes” with hyperglycemia and glycosuria.
V, VERTES, J, ANGELES, Y, KANTER
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Frontiers in Endocrinology, 2022 BackgroundMultiple endocrine neoplasia type 2A (MEN2A) is a rare syndrome that presents as medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism.
Yaohan Li +5 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.
and William M. Manger Md, Ray W. Gifford
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Targeting heat shock protein 90 for the treatment of malignant pheochromocytoma. [PDF]
PLoS ONE, 2013 Metastatic pheochromocytoma represents one of the major clinical challenges in the field of neuroendocrine oncology. Recent molecular characterization of pheochromocytoma suggests new treatment options with targeted therapies.
Alessio Giubellino +9 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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IJU Case Reports, 2022 Introduction Patients with multiple endocrine neoplasia type 2A (MEN2A) harboring a pathological variant in the RET gene are characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and hyperparathyroidism.
Koshiro Nishimoto +11 more
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Pheochromocytoma with Takotsubo Syndrome and acute heart failure: a case report
World 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
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Frontiers 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
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Clinical 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
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