A case of pheochromocytoma presenting as syncope due to long QT syndrome
Artigo
| IMSEAR
| ID: sea-193948
ABSTRACT
Pheochromocytoma, a catecholamine secreting tumour, is rare and we are presenting such a case who presened with syncopal episodes due to arrhythmias associated with the tumour. The patient was managed with pharmacologic and surgical treatment.
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Índice:
IMSEAR (Sudeste Asiático)
Ano de publicação:
2018
Tipo de documento:
Artigo
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