Title: A Rare Presentation of Pheochromocytoma
Authors: Rajiv Mohan Nannapaneni, Chandu Meena, Sreesivakumar Raja Addagalla, Udayabhaskar Pamarthi
DOI: https://dx.doi.org/10.18535/jmscr/v8i3.24
Abstract
Pheochromocytomas and paragangliomas are catecholamine-producing tumors derived from the sympathetic and parasympathetic nervous system. These tumors may arise sporadically or be inherited as features of multiple endocrine neoplasia type 2, von hippel-Lindau disease, or several other pheochromocytoma-associated syndromes. The diagnosis of pheochromocytomas identifies a potentially correctable cause of hypertension, and their removal can prevent hypertensive crisis that can be lethal.The clinical presentation is variable, ranging from an adrenal incidentaloma to a hypertensive crisis with associated cerebrovascular or cardiac complications.
Keywords: PRES, Pheochromocytoma,Vonhippel Lindau.
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