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Pheochromocytoma is a rarely seen neoplasm, and orginating from neural crest chromoffin cells which are responsible from producing, storing and secretion of catecholamines. Patients may refers to hospitals(or emergency services) with headache, sweating, palpitations and seizure attacks. Sometime the patients may be asemtomatic and the diagnose is esteblished incidentally. It is thought that if there are having distant metastasis, recurrent attacks and invasion to peripheral tissues, the disease is malign. The hypertension induced from pheochromocytoma can be treated effectively by some drugs. It may leads to mortality, if the patient’s diagnosis is not made timely or given treatment is inaccurate.
Alan : Sağlık Bilimleri
Dergi Türü : Ulusal
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