| Literature DB >> 16575763 |
Konrad Szosland1, Barbara Kopff, Andrzej Lewiński.
Abstract
Pheochromocytoma is a rare tumor derived from chromaffin cells, which produces catecholamins. The presence of this tumor is considered a cause of secondary hypertension, arrhythmias, sweating and also, but very rarely, mental disorders. Update diagnostic methods of pheochromocytoma are summarized in this article. Pheochromocytoma also coexists with endocrinological syndroms, e.g. multiple endocrine neoplasia type 2 (MEN 2). Studies confirm genetic background of pheochromocytoma occurrence.Entities:
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Year: 2006 PMID: 16575763
Source DB: PubMed Journal: Endokrynol Pol ISSN: 0423-104X Impact factor: 1.582