Abstract

BackgroundVisceral leishmaniasis (VL) is a protozoan disease, which is responsible for 200.000–400.000 yearly infections worldwide. If left untreated, the fatality rate can be as high as 100% within 2 years. 90% of cases occur in just six countries: India, Bangladesh, Sudan, South Sudan, Ethiopia and Brazil. It is thus a disease rarely seen by physicians in Europe or North America. We report on the fatal case of VL in an 80-year-old immunosuppressed patient who presented with a latency of over 15 years after having visited an endemic region. This is the first report showing such extreme latency of VL in a European traveller. This case is furthermore unusual because it suggests primary treatment failure to liposomal amphotericin B.Case presentationAn 80-year-old man who was on immunosuppressive treatment due to a non-specific inflammatory disease of the liver and kidney presented to our hospital with recurrent fever, fatigue and bloody diarrhoea. Histopathological analysis from a colon biopsy showed intracellular amastigotes. The diagnosis of VL was confirmed by polymerase-chain-reaction (PCR) of the colon biopsy. PCR was also performed in plasma, a bronchopulmonary lavage, a lymph node, liver and bone marrow biopsy and proved L. donovani as causative species. The disseminated infection was unresponsive to treatment with liposomal amphotericin B as recommended in immunosuppressed individuals despite stopping immunosuppressive treatment.ConclusionImported cases of VL to non-endemic regions are increasing due to extensive international travel and migration. Furthermore, the increase of elderly patients and immunosuppressed individuals, secondary to HIV, post-transplant and chemotherapeutic agents, has resulted in an increase of VL also in endemic regions of Europe. It is thus important for physicians to be able to recognize the infection. This case also demonstrates treatment failure to amphotericin B, which was only a known problem in patients with HIV until now. The knowledge of this as a possible complication is important for specialists treating the disease.

Highlights

  • Visceral leishmaniasis (VL) is a protozoan disease, which is responsible for 200.000–400.000 yearly infections worldwide

  • Visceral leishmaniasis (VL; known as “kala-azar”) is a neglected parasitic disease caused by the protozoans Leishmania donovani and L. infantum

  • Worldwide 0,2 to 0,4 million new clinical cases are diagnosed annually, 90% of these occurring in just six countries: India, Bangladesh, Sudan, South Sudan, Ethiopia and Brazil [1, 2]

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Summary

Conclusion

International travelling has led to an increase of imported leishmaniasis (though mainly cutaneous forms) in non-endemic countries, making the recognition of this parasitic infection important, especially since many physicians are not familiar with this disease [13]. VL should always be included in the differential diagnosis, especially in patients with a travel history to endemic areas several decades ago and not presenting initially with the cardinal symptoms of the disease. Patients requiring prolonged treatment with immunosuppressant drugs should undergo a detailed history of travel prior to the start of the medication, and tests investigating tuberculosis and tropical diseases such as leishmaniasis and strongyloides should be considered. Author details 1Department of Infectious Diseases, Bern University Hospital (Inselspital), University of Bern, PKT2B, CH-3010 Bern, Switzerland. Author details 1Department of Infectious Diseases, Bern University Hospital (Inselspital), University of Bern, PKT2B, CH-3010 Bern, Switzerland. 2Swiss Tropical and Public Health Institute, Basel, Switzerland. 3University of Basel, Basel, Switzerland. 4Department of Nephrology, Bern University Hospital (Inselspital), University of Bern, Bern, Switzerland. 5Institute of Pathology, University of Bern, Bern, Switzerland

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