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20 Οκτ 2019 · The surgical approach and extent of adrenalectomy is personalized based on multiple factors including germline genetic test results, the size of the tumor, body mass index, surgeon experience, and the likelihood of malignancy.
- Pheochromocytoma - Surgical Treatment - NCBI Bookshelf
Pheochromocytomas are relatively uncommon tumors, with a...
- Pheochromocytoma - Surgical Treatment - NCBI Bookshelf
Pheochromocytomas are relatively uncommon tumors, with a prevalence of 0.3% to 0.95% in autopsy series. Patients with pheochromocytomas have a potentially curable cause of hypertension and, if undetected, pheochromocytomas present a high risk of morbidity and mortality especially during surgical procedures and pregnancy.
6 Ιουλ 2023 · Pheochromocytoma (PCC) is a rare catecholamine-secreting tumor of adrenal origin. When it is extra-adrenal, it is referred to as paraganglioma. PCC is the cause of hypertension in 1 in 500 adults. These tumors are usually diagnosed by the 4th to 5th decade and are found equally in both genders.
6 Απρ 2017 · Pheochromocytomas are rare neuroendocrine tumors that produce and store catecholamines. Without adequate preparation, the release of excessive amounts of catecholamines, especially during anesthetic induction or during surgical removal, can produce life-threatening cardiovascular complications.
1 Μαρ 2024 · They include high blood pressure, headache, sweating and symptoms of a panic attack. If a pheochromocytoma isn't treated, serious or life-threatening damage to other body systems can happen. Surgery to remove a pheochromocytoma often returns blood pressure to a healthy range.
30 Αυγ 2024 · Pheochromocytoma is a rare neuroendocrine tumor of the adrenal glands. It can present with palpitations, diaphoresis, pallor, and paroxysmal hypertension. Risk factors include multiple endocrine neoplasia type 2, Von Hippel-Lindau syndrome, and neurofibromatosis type 1. Diagnosed by increased levels of metanephrines and normetanephrines.
8 Μαΐ 2023 · Objective. The aim of this review was to provide a practical approach for clinicians regarding the diagnosis and management of pheochromocytomas and paragangliomas (PPGLs). Methods. A literature search of PubMed was carried out using key words, including pheochromocytoma, paraganglioma, treatment, diagnosis, screening, and management.
