TY - JOUR
T1 - Successful treatment using corticosteroids in early phase of eosinophilic myocarditis with eosinophilic granulomatosis with polyangiitis
AU - Hase, Hiromu
AU - Yamamoto, Tatsuhiro
AU - Saito, Tetsuya
AU - Yamazaki, Hiroyuki
AU - Kuno, Toshiki
AU - Tabei, Ryota
AU - Kodaira, Masaki
AU - Motoda, Hiroyuki
AU - Numasawa, Yohei
N1 - Publisher Copyright:
© 2016 Japanese College of Cardiology
PY - 2016/12/1
Y1 - 2016/12/1
N2 - We report the case of a 50-year-old man with eosinophilic myocarditis and bronchial asthma treated successfully with prednisolone. He was initially diagnosed with eosinophilia, and complained of acute chest pain with electrocardiographic changes and elevation of cardiac enzymes. Coronary angiography showed no atherosclerotic changes; therefore, we performed endomyocardial biopsy and started oral prednisolone therapy immediately. His general condition improved with the disappearance of eosinophilia upon treatment. He was finally diagnosed with eosinophilic granulomatosis with polyangiitis complicated by eosinophilic myocarditis. This case report highlights that eosinophilic myocarditis may occur in association with systemic disease, and early steroid therapy is essential. <Learning objective: We report the case of a 50-year-old man diagnosed with eosinophilic granulomatosis with polyangiitis complicated by eosinophilic myocarditis. This was a rare case of eosinophilic granulomatosis with polyangiitis with eosinophilic infiltration that was observed pathologically in multiple organs, including the myocardium. This case report highlights that eosinophilic myocarditis may occur in association with systemic disease, and early steroid therapy is essential.>
AB - We report the case of a 50-year-old man with eosinophilic myocarditis and bronchial asthma treated successfully with prednisolone. He was initially diagnosed with eosinophilia, and complained of acute chest pain with electrocardiographic changes and elevation of cardiac enzymes. Coronary angiography showed no atherosclerotic changes; therefore, we performed endomyocardial biopsy and started oral prednisolone therapy immediately. His general condition improved with the disappearance of eosinophilia upon treatment. He was finally diagnosed with eosinophilic granulomatosis with polyangiitis complicated by eosinophilic myocarditis. This case report highlights that eosinophilic myocarditis may occur in association with systemic disease, and early steroid therapy is essential. <Learning objective: We report the case of a 50-year-old man diagnosed with eosinophilic granulomatosis with polyangiitis complicated by eosinophilic myocarditis. This was a rare case of eosinophilic granulomatosis with polyangiitis with eosinophilic infiltration that was observed pathologically in multiple organs, including the myocardium. This case report highlights that eosinophilic myocarditis may occur in association with systemic disease, and early steroid therapy is essential.>
KW - Endomyocardial biopsy
KW - Eosinophilic granulomatosis with polyangiitis
KW - Eosinophilic myocarditis
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U2 - 10.1016/j.jccase.2016.08.006
DO - 10.1016/j.jccase.2016.08.006
M3 - Article
AN - SCOPUS:84995676310
SN - 1878-5409
VL - 14
SP - 177
EP - 180
JO - Journal of Cardiology Cases
JF - Journal of Cardiology Cases
IS - 6
ER -