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Published on: April 7, 2015
Insidious clinical presentation of uncommon infective endocarditis caused by Cardiobacterium species
Francesco Bassani1,2, Gabriele Pagani1, Marco Franzetti1
1Infectious Diseases Unit, ASST Ovest Milanese, Ospedale di Legnano (MI), Italy.
Insights
Infective endocarditis (IE) caused by Cardiobacterium species in young men presents insidiously, often with atypical symptoms. Early diagnosis and treatment are crucial for managing this uncommon but serious condition.
Area of Science:
- Infectious Diseases
- Cardiology
- Microbiology
Background:
- Infective endocarditis (IE) is a severe infection, typically caused by Gram-positive bacteria.
- Cardiobacterium species, part of the HACEK group, are uncommon causes of IE.
Purpose of the Study:
- To describe two unique cases of Cardiobacterium spp. endocarditis in young men.
- To review literature on HACEK-related IE and discuss diagnostic and therapeutic challenges.
Main Methods:
- Case report presentation.
- Literature review focusing on HACEK group pathogens and IE.
Main Results:
- Two cases of Cardiobacterium spp. IE in young men are detailed, one with a myxomatous mitral valve and neurological symptoms, the other with atrial myxoma.
- HACEK IE often presents insidiously, with atypical symptoms, and a high prevalence of congenital cardiac malformations.
- Blood cultures may show delayed positivity (under 5 days) compared to typical IE pathogens.
- Surgical intervention is common, with quinolones emerging as an alternative to cephalosporins.
Conclusions:
- Cardiobacterium spp. IE, though less fatal than other IE types, carries a high risk of complications and often presents atypically.
- Awareness of HACEK group pathogens is important for diagnosing IE, especially in patients with cardiac abnormalities and non-specific symptoms.
Abstract:
Infective endocarditis (IE) is a fatal disease caused by a wide range of pathogens, with a strong prevalence of Gram-positive bacteria. In this paper we describe two peculiar cases of Cardiobacterium spp. endocarditis in young men. These case reports emphasize the insidious clinical presentation of HACEK IE and lead to a brief review of the literature and discussion on this uncommon cause of infective endocarditis. One case is a man with a prior diagnosis of myxomatous mitral valve, presenting with neurological symptoms and a mycotic aneurysm of the right anterior cerebral artery. The second case was a man with no prior medical history, presenting with fever, lumbar and right-leg pain, which led to a diagnosis of atrial myxoma. The presence of congenital cardiac malformations and an insidious onset with early presentation but unusual or non-specific symptoms are evidenced with a high prevalence in this group of patients. The diagnostic workup including cultural examinations are analyzed in the discussion. We noticed, in accordance with recent literature, a time to positivity of blood cultures longer than for typical agents, but mostly inferior to 5 days. The majority of the reported cases went to surgery, while therapeutical regimens alternative to cephalosporins, especially quinolones, are recently gaining interest. While mortality rates are lower than those observed in other cases of IE, Cardiobacterium spp. IE is characterized by a high burden of complications, leading to an often-atypical presentation.
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