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Published on: August 8, 2022
Actinobacillus endocarditis associated with hypertrophic cardiomyopathy
Vanda Cristina Jorge1, Ana Carolina Araújo, Ana Grilo
1Department 2, Curry Cabral's Hospital, Lisbon, Portugal. vandacristinajorge@gmail.com
Insights
Infective endocarditis caused by Actinobacillus actinomycetemcomitans is rare but serious. This case highlights the challenges in diagnosing and managing this infection, emphasizing the need for prompt surgical intervention.
Area of Science:
- Infectious Diseases
- Cardiology
- Microbiology
Background:
- Infective endocarditis (IE) poses complex clinical and management challenges.
- Actinobacillus actinomycetemcomitans (Aa) accounts for 5-10% of native valve IE.
- Aa infections are characterized by slow growth, potential for negative cultures, and systemic embolism.
Observation:
- A 59-year-old man with hypertrophic cardiomyopathy presented with fever of unknown origin after dental work.
- Transesophageal echocardiography confirmed mitral valve endocarditis.
- Blood cultures eventually isolated Actinobacillus actinomycetemcomitans.
Findings:
- The patient experienced multiple septic embolic events including skin, cerebral abscesses, spondylodiscitis, and uveitis despite antibiotic treatment.
- Surgical intervention was necessary, involving myectomy and mitral valve replacement with a mechanical prosthesis.
Implications:
- This case underscores the importance of considering rare pathogens like Aa in IE, especially with specific risk factors.
- Early and aggressive management, including surgical intervention, is crucial for favorable outcomes in complex IE cases.
- Multidisciplinary collaboration is essential for managing challenging IE presentations.
Abstract:
Infective endocarditis can be associated with complex clinical presentations, sometimes with a difficult multi-disciplinary management. Actinobacillus actinomycetemcomitans belongs to the Haemophilus species, Actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens and Kingella species group, responsible for 5% to 10% of infective endocarditis in native heart valves. These organisms have slow fastidious growth pattern, often associated with negative cultures, and cause systemic embolism with abscess formation. The authors present the case of a 59-year-old man, admitted due to fever of unknown origin, with a personal history of obstructive hypertrophic cardiomyopathy and recent dental manipulation. The diagnosis of mitral valve's endocarditis was established after a transoesophageal ecocardiography, with a late isolation of A actinomycetemcomitans in blood culture. Despite the institution of antibiotic therapy, the patient suffered from multiple episodes of septic embolism: skin, mucosae, cerebral abscesses, spondylodiscitis and uveitis. He was submitted to heart surgery with miectomy and replacement of the native mitral valve by a mechanical prosthesis, while on antibiotics.
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