A case of pheochromocytoma presenting as syncope due to long QT syndrome
Article
| 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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Année:
2018
Type:
Article
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