scholarly journals EOSINOPHILIC MYOCARDITIS ASSOCIATED WITH HYPEREOSINOPHILIC SYNDROME

2019 ◽  
Vol 73 (9) ◽  
pp. 2186
Author(s):  
Junya Komatsu ◽  
Ayaka Machida ◽  
Hikaru Imafuku ◽  
Ryota Kida ◽  
Yoshihiro Ohkawa ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Hanyin Wang ◽  
John K. Erban

We present the case of a 48-year-old female with acute onset altered mental status, who was found to have eosinophilia, elevated troponin, and embolic strokes. Extensive testing for autoimmune, infectious, and coronary artery etiologies was unremarkable. After a cardiac MRI revealed focal myocardial hyperenhancement, the patient underwent an endomyocardial biopsy with findings consistent with eosinophilic myocarditis. The patient was diagnosed of idiopathic hypereosinophilic syndrome and started on prednisone and apixaban. Our case highlights the importance of considering hypereosinophilic syndrome when eosinophilia is associated with multisystem impairments, as tissue biopsy is usually required to diagnose this rare condition.


Imaging ◽  
2021 ◽  
Author(s):  
Laura Ceriello ◽  
Antonino Scarinci ◽  
Cesare Mantini ◽  
Sabina Gallina ◽  
Filippo Cademartiri ◽  
...  

Abstract A 27-years-old female with multiple autoimmune disorders presented to our cardiology unit for acute chest pain and worsening dyspnoea. Admission blood tests revealed increased serum levels of high-sensitive cardiac troponin, eosinophilic count and C-reactive protein. Laboratory findings, low QRS voltages by ECG, mildly reduced left ventricular systolic function in the context of pseudohypertrophy, mild and diffuse late gadolinium enhancement associated with markedly increased native T1 and T2 mapping levels assessed by echocardiography and cardiovascular magnetic resonance imaging, raised the suspicion of massive eosinophilic myocarditis, subsequently confirmed by histological examination of endomyocardial biopsy. Prompt initiation of immunosuppressive treatment allowed swift regression of myocardial inflammation and full recovery of left ventricular systolic function within one month. After ruling-out clonal myeloid disorder, lymphocyte-variant and reactive hypereosinophilia, the young lady was eventually diagnosed with idiopathic hypereosinophilic syndrome. This case report turns the spotlight on the role and importance of advanced multi-modality cardiovascular imaging for raising clinical suspicion of acute eosinophilic myocarditis, guiding diagnostic work-up and monitoring response to treatment.


2020 ◽  
Vol 81 (1) ◽  
pp. 25
Author(s):  
Rui Assis ◽  
Andreia Brito

2019 ◽  
Vol 15 (1) ◽  
pp. 8-12 ◽  
Author(s):  
Muhammad Ali Chaudhry ◽  
Luanda Grazette ◽  
Andrew Yoon ◽  
Adrian Correa ◽  
Michael W. Fong

Background:Acute eosinophilic myocarditis (EM) is a rare form of heart failure that is characterized by myocardial eosinophilic infiltration usually in association with peripheral eosinophilia. The underlying cause is variable and can include allergic reactions, parasitic infection, idiopathic hypereosinophilic syndrome, malignancy, Loeffler’s syndrome, Churg-Strauss syndrome (CSS), early giant cell myocarditis and malignancy. The course is potentially fatal, and early diagnosis and treatment with steroids is essential.Conclusion:Here, we present an illustrative case of eosinophilic myocarditis secondary to CSS followed by a brief review of epidemiology, pathogenesis, diagnosis and treatment of both disease entities.


2011 ◽  
Vol 86 (7) ◽  
pp. 607-608 ◽  
Author(s):  
Michael H. A. Roehrl ◽  
Mariam P. Alexander ◽  
Stephen B. Hammond ◽  
Marianna Ruzinova ◽  
Julia Y. Wang ◽  
...  

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