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1.
Eur Rev Med Pharmacol Sci ; 27(23): 11479-11495, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-38095396

RESUMO

Acute myocarditis (AM) is an inflammatory affliction of the heart muscle characterized by recent onset with a broad spectrum of clinical manifestations that globally affect millions of individuals, notably children and young adults. The absence of distinct patterns of onset or predictable progression poses a significant threat to survival, potentially leading to advanced heart failure and malignant arrhythmias. Myocardial fibrosis, a hallmark of myocardial remodeling, is increasingly recognized as a contributor to adverse outcomes in acute myocarditis cases. Advances in molecular and immunological techniques have highlighted the intricate interplay between viral infections, dysregulated immune responses, and genetic susceptibility. Currently, there is no clear consensus for diagnosis or ongoing follow-up in pediatric patients. The conventional diagnostic tool, endomyocardial biopsy (EMB), considered the gold standard, has been complemented by the effectiveness of cardiac magnetic resonance imaging (CMRI) techniques. Given the procedural complexities and associated complications, there is a pressing need to explore non-invasive alternatives. In this context, biomarkers emerge as promising contenders by evaluating both the inflammatory processes and cardiac remodeling, providing valuable observations into disease severity, progression, and treatment response. Therapeutic strategies in these cases, focusing on the specific pathways or immune components associated with the etiologies, have exhibited promise for better outcomes. Acute myocarditis in children remains a multifaceted clinical challenge, necessitating a comprehensive understanding of its pathophysiology, diagnosis, and management. This review aims to delve into novel insights surrounding the pathophysiology, diagnosis, and management of acute myocarditis in pediatric patients.


Assuntos
Cardiomiopatias , Insuficiência Cardíaca , Miocardite , Humanos , Criança , Miocardite/diagnóstico , Miocardite/terapia , Miocardite/complicações , Miocárdio/patologia , Coração , Cardiomiopatias/patologia , Insuficiência Cardíaca/patologia , Biópsia/métodos
2.
Niger J Clin Pract ; 22(7): 1022-1025, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31293271

RESUMO

Paget-Schroetter syndrome (PSS), or effort thrombosis, refers to axillary and/or subclavian vein thrombosis associated with repetitive effort of the superior limbs, and is rare in the pediatric population. We report the case of a previously healthy 15-year-old boy who presented with a painful and swollen right arm after throwing firecrackers. Doppler ultrasound showed extensive right subclavian and axillary vein thrombosis. Anticoagulation therapy was started and had favorable evolution. We emphasize that PSS must be included in the differential diagnosis of a swollen arm.


Assuntos
Anticoagulantes/uso terapêutico , Veia Subclávia/diagnóstico por imagem , Ultrassonografia Doppler/métodos , Trombose Venosa Profunda de Membros Superiores/diagnóstico por imagem , Trombose Venosa/diagnóstico por imagem , Acenocumarol/uso terapêutico , Adolescente , Enoxaparina/uso terapêutico , Humanos , Masculino , Terapia Trombolítica , Resultado do Tratamento , Trombose Venosa Profunda de Membros Superiores/tratamento farmacológico , Trombose Venosa Profunda de Membros Superiores/etiologia , Trombose Venosa/tratamento farmacológico , Trombose Venosa/etiologia
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