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Mucorales endocarditis is an extremely rare and devastating disease, with few cases reported in the literature. The infection is predominantly found in immunocompromised patients, although a few cases involving immunocompetent individuals have been reported. We reviewed all cases of mucor endocarditis reported to date with a focus on demographics, clinical presentations, and the range of predisposing conditions, including immunosuppressive states, recent surgery, and cardiac device implantation. The management included a combination of radical surgeries, systemic antifungal therapy, and, in some cases, lifelong suppressive oral antifungals. Despite such aggressive forms of treatment, the survival rate remained exceedingly low, reflecting the poor prognosis of this illness. The current review provides an insight into the clinical features, treatment challenges, and outcomes of mucor endocarditis to guide future diagnostic and therapeutic approaches.
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http://dx.doi.org/10.1097/CRD.0000000000001026 | DOI Listing |
Cardiol Rev
September 2025
Division of Infectious Diseases, Department of Medicine, New York Medical College and Westchester Medical Center, Valhalla, NY.
Mucorales endocarditis is an extremely rare and devastating disease, with few cases reported in the literature. The infection is predominantly found in immunocompromised patients, although a few cases involving immunocompetent individuals have been reported. We reviewed all cases of mucor endocarditis reported to date with a focus on demographics, clinical presentations, and the range of predisposing conditions, including immunosuppressive states, recent surgery, and cardiac device implantation.
View Article and Find Full Text PDFEmerg Infect Dis
November 2023
We report a rare case of aorto-bi-iliac prosthetic allograft mucormycosis in a 57-year-old immunocompetent patient in France. Outcome was favorable after surgery and dual antifungal therapy with liposomal amphotericin B and isavuconazole. In a literature review, we identified 12 other cases of prosthetic vascular or heart valve mucormycosis; mortality rate was 38%.
View Article and Find Full Text PDFSurg Case Rep
September 2022
Division of Gastroenterological, Hepato-Biliary-Pancreatic, Transplantation and Pediatric Surgery, Department of Surgery, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, 390-8621, Japan.
Rinsho Ketsueki
August 2022
Department of Hematology and Oncology, Japanese Red Cross Society Himeji Hospital.
A 62-year-old female was presented to the hospital of the current study for pancytopenia and was diagnosed with severe aplastic anemia. She was treated with a combination therapy of antithymocyte globulin, cyclosporine A, and eltrombopag. The patient also presented with febrile neutropenia after commencement of the treatment and did not respond to the various antibiotics and antifungal agents.
View Article and Find Full Text PDFDiagnostics (Basel)
March 2022
Department of Pediatric Cardiology, "Marie Curie" Emergency Children's Hospital, 041451 Bucharest, Romania.
spp. is a group of fungi belonging to the order. Cases of fungal endocarditis are sporadic, but more frequent in immunocompromised patients.
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