Pheochromocytoma and Catecholamine Crisis

aciltip-10-2-kapak-wos

Rümeysa BAYAZIT KESKİNa , Fatih Ahmet KAHRAMANa

aAnkara Bilkent City Hospital, Clinic of Emergency Medicine, Ankara, Türkiye

ABSTRACT
Pheochromocytoma presents in different clinical settings ranging from asymptomatic to nonspecific findings such as hypertension, tachycardia, sweating, headache which may be confused with other diagnoses and even shock. It may occur spontaneously or hereditarily. It is difficult to make a diagnosis in emergency departments, but early diagnosis and initiation of correct treatment is lifesaving, especially in patients with catecholamine crisis. Supporting laboratory tests with imaging findings in suspected patients makes the diagnosis. Curative treatment is surgical, and it is essential to suppress adrenergic activity before surgery.
Keywords: Pheochromocytoma; catekolamines; neuroendocrine tumor

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