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Isolated left ventricular non-compaction cardiomyopathy complicated by acute ischemic stroke: A rare case repor

INTRODUCTION: and importance: Isolated left ventricular noncompaction cardiomyopathy (LVNC), uncommon type of primary hereditary cardiomyopathy. It is a spongy morphological appearance of the myocardium that occurs largely in the LV. CASE PRESENTATION: We discuss here a case of 19 years old female w...

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Detalles Bibliográficos
Autores principales: Ahmed, Said Abdirahman, Karataş, Mesut, Öcal, Lütfi, Hassan, Mohamed Sheikh, Mohamud, Mohmed Abdullahi, Hassan, Mohamed Omar, Dirie, Abdirahman Mohamed Hassan, Waberi, Mohamud Mire, Ali, Abdijalil Abdullahi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486750/
https://www.ncbi.nlm.nih.gov/pubmed/36147147
http://dx.doi.org/10.1016/j.amsu.2022.104543
Descripción
Sumario:INTRODUCTION: and importance: Isolated left ventricular noncompaction cardiomyopathy (LVNC), uncommon type of primary hereditary cardiomyopathy. It is a spongy morphological appearance of the myocardium that occurs largely in the LV. CASE PRESENTATION: We discuss here a case of 19 years old female with no known past medical history who present with Shortness of breath (SOB) and left sided weakness following delivery. Bedside Echocardiography demonstrated Left ventricular trabiculation with reduced ejection fraction. While brain Computed tomography showed acute ischemic stroke primly due to non-compaction cardiomyopathy as the embolic. Patient was discharged after successfully managed. CLINICAL DISCUSSION: Left ventricular non-compaction cardiomyopathy (LVNC) is characterized by progressive ventricular trabeculation and deep intratrabecular recesses caused by the functional arrest of myocardial maturation, which is a rare case of congenital cardiomyopathy. Our patient had isolated non-compaction cardiomyopathy of the type that was complicated by an acute ischemic stroke and was treated accordingly. CONCLUSION: It is usually associated with congenital heart disease, but isolated left ventricular non-compaction cardiomyopathy is very uncommon.