Abstract
Background
Tularemia, a zoonotic disease caused by Francisella tularensis, can cause a broad spectrum of disease in humans including six major clinical presentations: the ulceroglandular, glandular, oculoglandular, oropharyngeal, typhoidal and pneumonic form. The epidemiology and ecology and thus transmission of tularemia are complex, depending on conditions unique to specific locations.
Case series and methods
Thirteen cases with different forms of the disease and one very rare case of a myocarditis are reported, discussed, and reviewed within the scope of current literature.
Conclusion
Tularemia is a rare, but emerging disease in Central Europe with glandular and ulceroglandular disease as its predominant forms. Transmission is mainly caused by contact with lagomorphs, rodents and tick bites. However, domestic cats may play an important role in transmission too. Myocarditis is probably a worldwide, but very rare manifestation of tularemia.
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Abbreviations
- GP:
-
General practitioner
- ER:
-
Emergency room
- CRP:
-
C-reactive protein
- WBC:
-
White blood cells
- AST:
-
Aspartate aminotransferase
- ALT:
-
Alanine aminotransferase
- LDH:
-
Lactate dehydrogenase
- CK:
-
Creatine kinase
- U/ml:
-
Units per milliliter
- U/l:
-
Units per liter
- G/l:
-
Giga per liter
- mg/l:
-
Milligram per liter
- ng/l:
-
Nanogram per liter
- PCR:
-
Polymerase chain reaction
- ECG:
-
Electrocardiogram
- CT:
-
Computed tomography
- MRI:
-
Magnetic resonance imaging
- PET:
-
Positron emissions tomography
- I.V.:
-
Intravenous
- ELISA:
-
Enzyme-linked immunosorbent assay
- Bid:
-
Twice a day
- NSAID:
-
Nonsteroidal anti-inflammatory drugs
- Ssp.:
-
Subspecies
- DNA:
-
Deoxyribonucleic acid
- RNA:
-
Ribonucleic acid
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In particular, we would like to thank Nancy Landes and Carol Idone for the language editing.
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Frischknecht, M., Meier, A., Mani, B. et al. Tularemia: an experience of 13 cases including a rare myocarditis in a referral center in Eastern Switzerland (Central Europe) and a review of the literature. Infection 47, 683–695 (2019). https://doi.org/10.1007/s15010-019-01269-7
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DOI: https://doi.org/10.1007/s15010-019-01269-7