Evidence map›Paper›PMID 40996955›Full record

ArticleThe American journal of case reports2025

Native Aortic Valve Endocarditis Caused by Rothia mucilaginosa, Initially Misidentified as Neisseria sicca.

Tiffany S Liu, Austin Scro, Mustafa Awayda, Maroun Bou Zerdan

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Article in The American journal of case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tiffany S LiuDepartment of Medicine, State University of New York (SUNY) Upstate Medical University, Syracuse, NY, USA.
Austin ScroDepartment of Medicine, State University of New York (SUNY) Upstate Medical University, Syracuse, NY, USA.
Mustafa AwaydaDepartment of Medicine, State University of New York (SUNY) Upstate Medical University, Syracuse, NY, USA.
Maroun Bou ZerdanDepartment of Medicine, State University of New York (SUNY) Upstate Medical University, Syracuse, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Infective endocarditis is a potentially life-threatening disease predominantly affecting the heart valves. Common causative pathogens include Staphylococcus aureus and Streptococcus viridans. However, it can be caused by atypical organisms such as Rothia species (spp.). When Rothia spp. cause endocarditis, the organism often affects prosthetic valves and rarely native ones. We report a case of native aortic valve subacute endocarditis caused by R. mucilaginosa, initially misidentified as Neisseria sicca, in an immunocompromised middle-aged patient. CASE REPORT A 54-year-old man with histories of hemochromatosis, diabetes, hypertension, alcohol abuse, and smokeless tobacco use presented with 7 days of fever, intermittent cough, and headache. Diagnostic workup revealed a new systolic murmur, blood cultures positive for N. sicca, and a vegetation on the aortic valve noted on a transesophageal echocardiogram. He was diagnosed with subacute infective endocarditis using Duke criteria and discharged on 6 weeks of intravenous ceftriaxone. However, 1 day later, he presented to another facility with a new fever and had a chest X-ray showing atypical pneumonia. The initial blood isolates were re-identified as R. mucilaginosa. His hospital course was complicated by a small intraparenchymal hemorrhage and 2 embolic infarcts. He continued ceftriaxone and eventually recovered to baseline. CONCLUSIONS We present a case of an immunocompromised middle-aged man who developed subacute infective endocarditis caused by an atypical organism, R. mucilaginosa. Infective endocarditis should always be a differential diagnosis in patients presenting with fever of an unknown source.

Indexed as

Aortic ValveEndocarditis, BacterialMicrococcaceaeAnti-Bacterial AgentsDiagnosis, DifferentialDiagnostic ErrorsEchocardiography, TransesophagealHumansImmunocompromised HostMaleMiddle AgedNeisseriaNeisseriaceae InfectionsAnti-Bacterial Agents

Identifiers

PMID40996955
PMCPMC12482780

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.