Please use this identifier to cite or link to this item: https://cris.library.msu.ac.zw//handle/11408/6862
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHlupeni, Admireen_US
dc.contributor.authorAdebisi Adejolaen_US
dc.contributor.authorAmirseena Tolebeyanen_US
dc.contributor.authorJeramey Stewarten_US
dc.contributor.authorJoseph Fritzen_US
dc.date.accessioned2025-10-19T13:40:02Z-
dc.date.available2025-10-19T13:40:02Z-
dc.date.issued2025-
dc.identifier.urihttps://cris.library.msu.ac.zw//handle/11408/6862-
dc.description.abstractBackground Prosthetic valve endocarditis due to Histoplasma capsulatum is exceedingly rare and difficult to diagnose. Case Summary A 79-year-old man with a bioprosthetic mitral valve presented with subacute cognitive decline, pancytopenia, and hypercalcemia. He was afebrile and hemodynamically stable. Echocardiography showed vegetations on the valve. Initially, blood cultures were negative. Urine Histoplasma antigen and serum beta-D-glucan were positive, and fungal blood cultures later grew H capsulatum after 4 weeks of incubation. He was managed with liposomal amphotericin B followed by isavuconazole due to itraconazole contraindications. He gradually recovered without surgical intervention. Discussion This case illustrates the diagnostic and treatment complexities of Histoplasma endocarditis. Take-Home Messages In endemic regions, consider Histoplasma in culture-negative prosthetic valve endocarditis. Early diagnosis may rely on beta-D-glucan and H capsulatum urine antigen before cultures become positive. Isavuconazole is a viable alternative when itraconazole is not an option. Selected patients can be managed successfully without surgery.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofJACC: Case Reportsen_US
dc.subjectEchocardiographyen_US
dc.subjectEndocarditisen_US
dc.subjectMitral valveen_US
dc.subjectValve replacementen_US
dc.titleCulture-Confirmed Histoplasma Endocarditis on Bioprosthetic Mitral Valve Managed Successfully Without Surgeryen_US
dc.typeresearch articleen_US
dc.identifier.doihttps://doi.org/10.1016/j.jaccas.2025.105315-
dc.contributor.affiliationInternal Medicine Residency Department, St Luke’s Hospital, Chesterfield, Missouri, USA; Faculty of Medicine, Midlands State University, Senga, Gweru, Zimbabween_US
dc.contributor.affiliationInternal Medicine Residency Department, St Luke’s Hospital, Chesterfield, Missouri, USAen_US
dc.contributor.affiliationInternal Medicine Residency Department, St Luke’s Hospital, Chesterfield, Missouri, USAen_US
dc.contributor.affiliationInternal Medicine Residency Department, St Luke’s Hospital, Chesterfield, Missouri, USAen_US
dc.contributor.affiliationInternal Medicine Residency Department, St Luke’s Hospital, Chesterfield, Missouri, USAen_US
dc.relation.issn2666-0849en_US
dc.description.volume30en_US
dc.description.issue30en_US
dc.description.startpage1en_US
dc.description.endpage7en_US
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairetyperesearch article-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
Appears in Collections:Research Papers
Show simple item record

Page view(s)

58
checked on Oct 22, 2025

Download(s)

6
checked on Oct 22, 2025

Google ScholarTM

Check

Altmetric


Items in MSUIR are protected by copyright, with all rights reserved, unless otherwise indicated.