Xasanova, Nargis Qodirovna (2024) SPECIFIC FEATURES OF PHEOCHROMOCYTOMA. European Journal of Modern Medicine and Practice, 4 (10). pp. 297-303. ISSN 2795-921X
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Abstract
Pheochromocytomas and paragangliomas are catecholamine-producing tumors derived from the sympathetic or parasympathetic nervous system. These tumors may arise sporadically or be inherited as features of multiple endocrine neoplasia type 2 or several other pheochromocytoma-associated syndromes. The diagnosis of pheochromocytomas provides a potentially correctable cause of hypertension, and their removal can prevent hypertensive crises that can be lethal. The clinical presentation is variable, ranging from an adrenal incidentaloma to a patient in hypertensive crisis with associated cerebrovascular or cardiac complications
Item Type: | Article |
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Subjects: | R Medicine > R Medicine (General) |
Divisions: | Postgraduate > Master's of Management |
Depositing User: | Journal Editor |
Date Deposited: | 19 Dec 2024 07:52 |
Last Modified: | 19 Dec 2024 07:52 |
URI: | http://eprints.umsida.ac.id/id/eprint/14945 |
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