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Intern Med ; 62(17): 2565-2569, 2023 Sep 01.
Article in English | MEDLINE | ID: mdl-37316277

ABSTRACT

Multisystem inflammatory syndrome in adults (MIS-A) is a life-threatening disease that can develop weeks after coronavirus disease 2019 (COVID-19). MIS-A symptoms include multiorgan involvement, especially gastrointestinal tract and heart involvement, and Kawasaki disease-like symptoms. We herein report a 44-year-old Japanese man with MIS-A who had contracted COVID-19 five weeks ago and went into shock after acute gastroenteritis, acute kidney injury, and Kawasaki disease-like symptoms. Methylprednisone pulse and high-dose intravenous immunoglobulin resulted in recovery of shock and his renal function, but diffuse ST-segment elevation on electrocardiography and pericardial effusion with a fever emerged after therapy. Additional granulocyte-monocyte adsorptive apheresis successfully ameliorated the cardiac involvement.


Subject(s)
Blood Component Removal , COVID-19 , Connective Tissue Diseases , Mucocutaneous Lymph Node Syndrome , Male , Humans , Adult , COVID-19/complications , COVID-19/therapy , Monocytes , Systemic Inflammatory Response Syndrome/complications , Systemic Inflammatory Response Syndrome/therapy , Granulocytes
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