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Case report: Disseminated Scedosporium apiospermum infection with invasive right atrial mass in a heart transplant patient

Scedosporium apiospermum associated endocarditis is extremely rare. We report a case of a disseminated S. apiospermum infection with an invasive right atrial mass in a 52-year-old male, 11 months after heart transplantation, referred to our institution for an endogenous endophthalmitis with a one-mo...

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Detalles Bibliográficos
Autores principales: Bourlond, Baudouin, Cipriano, Ana, Regamey, Julien, Papadimitriou-Olivgeris, Matthaios, Kamani, Christel, Seidel, Danila, Lamoth, Frederic, Muller, Olivier, Yerly, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660239/
https://www.ncbi.nlm.nih.gov/pubmed/36386301
http://dx.doi.org/10.3389/fcvm.2022.1045353
Descripción
Sumario:Scedosporium apiospermum associated endocarditis is extremely rare. We report a case of a disseminated S. apiospermum infection with an invasive right atrial mass in a 52-year-old male, 11 months after heart transplantation, referred to our institution for an endogenous endophthalmitis with a one-month history of diffuse myalgias and fatigue. The patient had been supported two times with extracorporeal membrane oxygenation (ECMO) during the first three postoperative months. The echocardiography on admission revealed a mass in the right atrium attached to a thickened lateral wall. The whole-body [(18)F]FDG PET/CT revealed systemic dissemination in the lungs, muscles, and subcutaneous tissue. Blood cultures were positive on day three for filamentous fungi later identified as S. apiospermum. The disease was refractory to a 3-week dual antifungal therapy with voriconazole and anidulafungin in addition to reduced immunosuppression, and palliative care was implemented.