Ontology highlight
ABSTRACT:
SUBMITTER: Dai J
PROVIDER: S-EPMC5442980 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature

Dai Jin J Chen Shen-Jie SJ Yang Bing-Sheng BS Lü Shu-Min SM Zhu Min M Xu Yi-Fei YF Chen Jie J Cai Hong-Wen HW Mao Wei W
Journal of Zhejiang University. Science. B 20170501 5
Pheochromocytoma is a rare neuroendocrine tumor which derives from chromaffin cells of the adrenal gland or relevant to sympathetic nerves and ganglia. The clinical features of pheochromocytoma are various. Paroxysmal episodes of serious hypertension, headache, palpitation, and diaphoresis are the typical manifestations (Bravo, 2004). Hypotension shock, pulmonary edema, and acute coronary syndrome induced by pheochromocytoma are uncommon (Malindretos et al., 2008; Batisse-Lignier et al., 2015). ...[more]