Literature DB >> 28954750

Eosinophilic myocarditis: an often subtle and potentially under-recognised phenomenon.

John Joseph Coughlan1, Gerald Paul Fitzgerald2, Filza Gul3, Richard Liston4.   

Abstract

A 34-year-old woman presented to our service with chest pain, a troponin rise and dynamic ECG changes. Of note, she had complained of fatigue, feeling constitutionally unwell and a generalised rash in the days prior to her presentation. Her echocardiogram showed normal wall motion and preserved ejection fraction. Her eosinophil count, normal at presentation, rose to a peak of 12.21×105/L. She was haemodynamically stable throughout with no evidence clinically of congestive cardiac failure. CT coronary angiogram showed no obstructive coronary artery disease. Cardiac MRI demonstrated areas of late gadolinium enhancement consistent with myocarditis. A diagnosis of eosinophilic myocarditis was made. No tissue biopsy was performed due to the patchy myocardial involvement and high potential for low-yield biopsy. Our patient was treated conservatively and has made an excellent recovery. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  Eosinophilia; Myocarditis; cardiovascular medicine; haematology (including blood transfusion)

Mesh:

Year:  2017        PMID: 28954750      PMCID: PMC5747783          DOI: 10.1136/bcr-2017-221289

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  1 in total

1.  Fast spontaneous recovery from acute necrotizing eosinophilic myopericarditis without need for immunosuppressive therapy: a case report of a 27-year-old male.

Authors:  Michael Kindermann; Nitin Sood; Peter Ehrlich; Karin Klingel
Journal:  Eur Heart J Case Rep       Date:  2020-06-17
  1 in total

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