[Pheochromocytoma as a simulator of cardiac pathology].

Autor: Vallejo Herrera MJ; Servicio de Endocrinología, Hospital Regional de Málaga, Málaga, España; Servicio de Medicina Interna, Hospital Regional de Málaga, Málaga, España. Electronic address: mariajosevallejoherrera@gmail.com., Vallejo Herrera V; Servicio de Medicina Interna, Hospital Regional de Málaga, Málaga, España; Servicio de Radiodiagnóstico, Hospital Regional de Málaga, Málaga, España., Márquez Pérez V; Servicio de Radiodiagnóstico, Hospital Regional de Málaga, Málaga, España., Serrano Puche F; Servicio de Radiodiagnóstico, Hospital Regional de Málaga, Málaga, España., Vegas Vegas I; Servicio de Cardiología, Hospital Regional de Málaga, Málaga, España.
Jazyk: Spanish; Castilian
Zdroj: Hipertension y riesgo vascular [Hipertens Riesgo Vasc] 2024 Oct-Dec; Vol. 41 (4), pp. 260-263. Date of Electronic Publication: 2024 May 20.
DOI: 10.1016/j.hipert.2024.04.006
Abstrakt: Pheochromocytomas are rare neuroendocrine tumors that can present as hypertensive crises or serious cardiac and cerebrovascular complications that endanger the patient's life. Two unusual cases of adrenergic crises induced by pheochromocytoma with cardiovascular manifestations are presented, one with multiple complications/multiorgan failure, fatal outcome and definitive diagnosis in the post mortem autopsy, and another with a satisfactory evolution after diagnosis and appropriate treatment.
(Copyright © 2024 SEH-LELHA. Publicado por Elsevier España, S.L.U. All rights reserved.)
Databáze: MEDLINE
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