Cardiomyopathie dilatée compliquant un phéochromocytome d’évolution favorable après chirurgie : à propos d'un cas à Dakar « cas clinique avec revue de littérature »

IF 0.3 Q4 Medicine

Annales de cardiologie et d'angeiologie Pub Date : 2025-03-10 DOI:10.1016/j.ancard.2025.101866

Wn Mboup , Sct Ndao , M Sarr , M Faye , Pm Guisse , Mm Ka , Mn Sarr , K Dia

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引用次数: 0

Abstract

Introduction

Dilated cardiomyopathy is a rare and often little-known complication of pheochromocytoma, it is likewise exceptionally its discovery circumstance. This is usually an acute, reversible cardiomyopathy.We report the case of a 20-year-old young adult hospitalized for hypokinetic dilated cardiomyopathy with severe impairment of left ventricular ejection fraction (LVEF) to 17%. High blood pressure persisted despite antihypertensive treatment, and the heart failure syndrome was refractory to medical treatment.

Abdominal CT scan revealed a heterogeneous adrenal mass strongly suggestive of pheochromocytoma. Determination of plasma metanephrines and normetanephrines led to the diagnosis of pheochromocytoma. After surgery, the course was marked by stabilization of blood pressure, normalization of Doppler echocardiography and complete clinical remission.

He remained asymptomatic at one year.

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来源期刊

Annales de cardiologie et d'angeiologie 医学-外周血管病

CiteScore

0.60

自引率

0.00%

发文量

审稿时长

6-12 weeks

期刊介绍： Organe scientifique de référence fondé en 1951, les Annales de cardiologie et d''angéiologie abordent tous les domaines qui intéressent quotidiennement les cardiologues et les angéiologues praticiens : neurologie et radiologie vasculaires, hémostase, diabétologie, médecine interne, épidémiologie et prévention. Les Annales de cardiologie et d''angéiologie sont indexées aux grandes bases de données et publient rapidement, et en conformité avec les normes internationales de publication scientifique, des articles en français sur la pathologie cardiaque.