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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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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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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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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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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
doaj +1 more source
Composite pheochromocytoma associated with neurofibromatosis type 1
IJU 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
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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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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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