[Blue toe syndrome as a clinical finding of pheochromocytoma]
Medicina (B Aires) . 2018;78(5):368-371.
Fecha de la publicación: 01/01/2018
Autor: Vicente Mosquera Rey (1), Carmen Palomo Antequer (2), Carmen Cienfuegos Basanta (2), Amer Zanabili Al-Sibbai (3), Alba Fidalgo Navarro (2), Manuel Alonso Pérez (3)
Palabras clave: blue toe syndrome, catecholamines; digital necrosis, hypertensive crises, pheochromocytoma
PMID
- PMID: 30285931
Affiliations
1Servicio de Angiología y Cirugía Vascular, Hospital Universitario Central de Asturias (HUCA), Oviedo, España. E-mail: vimosre@gmail.com.
2Servicio de Medicina Interna, Hospital Universitario Central de Asturias (HUCA), Oviedo, España.
3Servicio de Angiología y Cirugía Vascular, Hospital Universitario Central de Asturias (HUCA), Oviedo, España.
Abstract
Pheochromocytomas are tumors that arise from chromaffin cells of the sympathetic nervous system and act by synthesizing and releasing catecholamines. They usually occur between the fourth and fifth decade of life and have a very wide clinical presentation. They occur only in 0.1-0.2% of the hypertensive population and represent a treatable and curable cause of arterial hypertension, as well as other symptoms derived from the uncontrolled secretion of catecholamines. Peripheral arterial ischemia secondary to massive amines release by a pheochromocytoma is a very uncommon condition. Here we report a case of pheochromocytoma manifested as blue finger syndrome in a patient with palpable distal pulses and history of poor blood pressure control despite treatment with two drugs.