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Campylobacter coli Myocarditis: a case report

Published online by Cambridge University Press:  06 December 2021

Sílvia A. Gomes*
Affiliation:
Pediatric Cardiology Service, Hospital de Santa Marta, Lisbon, Portugal
Conceição Trigo
Affiliation:
Pediatric Cardiology Service, Hospital de Santa Marta, Lisbon, Portugal
Fátima F. Pinto
Affiliation:
Pediatric Cardiology Service, Hospital de Santa Marta, Lisbon, Portugal
*
Address for correspondence: Dr. Sílvia A. Gomes, Pediatric Cardiology Service, Hospital de Santa Marta, Rua de Santa Marta 50, 1169-024, Lisbon, Portugal. Tel: +351 213594332. E-mail: silviacagomes@outlook.pt
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Abstract

We report the case of a 14-year-old male presented with raised myocardial injury biomarkers, on the workout, Campylobacter coli was identified on stool culture, treated with antibiotics with total resolution. Cardiac magnetic resonance showed interventricular septum and lateral wall hypokinesia and subepicardial delayed enhancement, with preserved ventricular systolic function. To our knowledge, this is the first report linking Campylobacter coli to myopericarditis in children.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Myocarditis is a challenging diagnosis due to the heterogeneity of clinical presentation and aetiology. Reference Caforio1,Reference Obafemi and Douglas2 Myocarditis has been associated with a variety of infections, metabolic, and immune disorders as well as exposure to drug treatment or radiation. Reference Imanaka-Yoshida3

Viral myocarditis is the most common aetiological cause. Reference Obafemi and Douglas2,Reference Moffatt, Moloi and Kennedy4 Although several microorganisms might be associated, Campylobacter infection has been infrequently implicated. Reference Obafemi and Douglas2,Reference Moffatt, Moloi and Kennedy4

Campylobacter jejuni is the most common species isolated in patients with diarrhoea, followed by Campylobacter coli. Reference Schiaffino, Colston and Paredes-Olortegui5 Complications as bacteriaemia or post-infectious sequelae, as cardiac involvement have been associated with enteritis. Reference Obafemi and Douglas2Reference Moffatt, Moloi and Kennedy4

To our knowledge, our report describes the first case of myocarditis associated with campylobacter coli enteritis in an adolescent.

Case report

The authors report the case of a healthy 14-year-old male who presented with a 4-day fever, abdominal pain, and profuse diarrhoea, without blood, mucus, or purulent stools. He also reported a 2-day persistent left lateral chest pain, non-radiating, without triggering factors. The patient had no significant medical history or risk factors for cardiac disease. He denied any recent travel, drug use, or sexual activity.

Patient was afebrile, mildly dehydrated. Heart rate and blood pressure were within normal range. On auscultation, there were no additional murmurs or rubs, and the remaining clinical observation was irrelevant.

The chest x-ray disclosed bilateral infiltrate. The electrocardiogram was normal. C-reactive protein was elevated (58.7 mg/dL) with a normal leukocyte count. Serum creatinine kinase (604 U/L) and high sensitivity troponin I (maximal value of 8443.3 pg/mL) were raised. Liver enzymes were mildly elevated, and serum electrolytes were unremarkable.

We assumed a presumptive diagnosis of myocarditis based on clinical presentation and significantly raised myocardial injury biomarkers. The echocardiogram demonstrated normal ventricular dimensions, mild mitral, tricuspid regurgitation, and preserved diastolic function, but with borderline ventricular systolic function (biplane Simpson’s ejection fraction 51% (GLS -16.1%). There was no pericardial or pleural effusion. The patient remained on bed rest and started therapy with enalapril and carvedilol.

During etiological investigation, Campylobacter coli was isolated on stool culture, while the remaining tests were negative. He started treatment with intravenous amoxicillin/clavulanic acid and gentamicin, based on the local antibiotic resistance. After antimicrobial sensitivity test, gentamicin was discontinued.

Four days after treatment, the patient remained asymptomatic with normalisation of myocardial injury biomarkers on the sixth day.

At discharge, the echocardiogram disclosed improvement of contractility, with systolic function within normal range (biplane Simpson’s ejection fraction 53%, GLS −16.3%). The patient completed 14 days of antibiotic therapy and maintained remaining therapy during outpatient follow-up.

Cardiac magnetic resonance showed normal left ventricle volumes with hypokinesia of the basal segments of the interventricular septum and lateral wall. Ventricular function was preserved. There was no pericardial effusion, thickening, or significant myocardial oedema. Subepicardial delayed enhancement (Fig 1) of the inferolateral wall of the left ventricle was observed, consistent with subacute myocarditis (Fig 2).

Figure 1. 2D myocardial late enhancement ventricular short axis.

Figure 2. 2D myocardial late enhancement three chambers left view.

Discussion

Myocarditis is an inflammatory condition of the myocardium. Reference Imanaka-Yoshida3 It presents from mild symptoms to life-threatening cardiogenic shock and ventricular arrhythmia. Dilated cardiomyopathy might be a late consequence, reported in 6–30% of patients with worsening cardiac function. Reference Caforio1,Reference Imanaka-Yoshida3

The incidence of myocarditis might be underdetermined due to variability of clinical presentation. Reference Blauwet and Cooper6 In the paediatric population, it can be a cause of sudden death or evolved to dilated cardiomyopathy, with the risk of death and heart transplantation persisting up to 12 years after diagnosis. Reference Imanaka-Yoshida3,Reference Blauwet and Cooper6

Although a rare cause, most common bacterial infections associated with myocarditis are Legionella, mycobacteria, streptococci, and staphylococci with Salmonella and Shigella mentioned in some case reports. Reference Obafemi and Douglas2,Reference Blauwet and Cooper6

Myocarditis associated with bacterial enteritis has only rarely been described, and the pathogenesis is unclear, raising questions whether the myocardial inflammation is caused by direct action of the bacteria or by toxic or immunological mechanisms. Reference Wanby and Olsen7

Campylobacter jejuni is the most common cause of human bacterial enteritis in developed countries. Reference Obafemi and Douglas2,Reference Moffatt, Moloi and Kennedy4 Infections often are asymptomatic and self-limited with rare extraintestinal complications, including arthritis, meningitis, or Guillain-Barré syndrome. Reference Hessulf, Ljungberg, Johansson, Lindgren and Engdahl8 Campylobacter, although uncommon, are increasingly recognised to be associated with myopericarditis, Reference Moffatt, Moloi and Kennedy4 with almost all cases reporting Campylobacter jejuni or fetus enteritis as the etiological pathogen is associated with cardiac injury. Reference Obafemi and Douglas2 Much effort has been invested to elucidate its pathogenic mechanism, although it remains unclear. Reference Moffatt, Moloi and Kennedy4,Reference Uzoigwe9

To our knowledge, this is the first report associating Campylobacter coli with myocarditis in a paediatric patient.

The diagnosis was supported by clinical presentation, raised myocardial injury biomarkers, and changes on cardiac magnetic resonance. We emphasise that a normal electrocardiogram does not exclude myocarditis; once its reported sensitivity is 47%. Reference Blauwet and Cooper6

Broad-spectrum antibiotic therapy was initiated due to the systemic involvement of the infection, Reference Moffatt, Moloi and Kennedy4 either by direct infection of the myocardium, an immune hypersensitivity reaction, or the effect of bacterial toxins. Reference Moffatt, Moloi and Kennedy4

Myocardial biopsy and analysis of pericardial fluid, demonstrating bacteria infiltration, support a direct infection pathophysiologic mechanism. Moffatt et al. reported two immunocompromised patients with myopericarditis and Campylobacter isolated in pericardial fluid, Reference Moffatt, Moloi and Kennedy4 while other reports did not identify C. jejuni on blood cultures. Reference Uzoigwe9

As described by other authors, immune-mediated aetiology was excluded, because of the short mediated time between the onset of gastrointestinal symptoms and those of myocardial injury. Reference Uzoigwe9 This short period favours a toxin-mediated mechanism, although there is no evidence of a specific Campylobacter-associated toxicity to the myocardium. Reference Wassenaar10

Myocardial biopsy remains the gold standard for the diagnosis of myocarditis; however, it is not performed routinely, due to known complications. Reference Caforio1

Cardiac magnetic resonance has become an important non-invasive alternative for assessment of patients with suspected myocarditis. Reference Imanaka-Yoshida3,Reference Blauwet and Cooper6 Although myocardial biopsy can demonstrate the inflammatory infiltrate associated with myocyte necrosis or damage required to the diagnosis of myocarditis, Reference Imanaka-Yoshida3 cardiac magnetic resonance diagnostic targets include functional and morphological abnormalities, as well as tissue pathology characteristic of myocardial injury. Reference Blauwet and Cooper6

Reported clinical outcomes for C. jejuni and C. coli-associated myopericarditis in adult patients appear favourable. Reference Moffatt, Moloi and Kennedy4

Conclusion

To our knowledge, this is the first report of myocarditis associated with Campylobacter coli infection in a paediatric patient. Although a rare cause of myocarditis remains, it should be considered in paediatric patients with enteric symptoms.

Acknowledgements

The authors are grateful to Marta António, MD, for her availability to help in the optimisation and selection of the images in this article.

Financial support

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Conflicts of interest

None.

Ethical standards

The authors declare that the procedures followed were in accordance with the regulations of the relevant clinical research ethics committee and with those of the Code of Ethics of the World Medical Association (Declaration of Helsinki).

References

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Figure 0

Figure 1. 2D myocardial late enhancement ventricular short axis.

Figure 1

Figure 2. 2D myocardial late enhancement three chambers left view.