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American Tegumentary Leishmaniasis

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Summary

American tegumentary leishmaniasis is an endemic anthropozoonosis undergoing expansion on the American continent. The disease is caused by several Leishmania species, and, thus, there are intraspecific parasitological dissimilarities that may generate different pathologies. Furthermore, in America, Leishmania spp. has diverse reservoirs (that may change continuously) and can use various vectors to infect humans and mammals. Antimonials are the drugs of choice for the treatment of American tegumentary leishmaniasis; however, their efficacy is not predictable, and this may be linked to parasite drug resistance. This is further complicated by the fact that the etiological parasitic species in America belong to both the Leishmania and the Viannia subgeni. For all these reasons, the identification of the etiological infectious agent – up to the species level – is fundamental for precise clinical diagnosis, for treatment and prognosis, and for control of the disease. The present chapter offers a description of American tegumentary leishmaniasis, a fundamental piece of knowledge for the comprehension of the challenges we face for leishmaniasis in times of drug resistance. As a way to better understand the unique scenario that America offers for leishmaniasis, some data related to the figures present in the Old World will be presented.

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Acknowledgments

The authors are grateful for the financial support received from the Coordination for Research, Faculty of Medicine, Universidad Central de Venezuela (UCV), and the Council for Scientific and Humanistic Research (CDCH), UCV. Likewise, they are grateful for the support conferred by the Alexander von Humboldt Foundation, Germany, to Alicia Ponte-Sucre.

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Correspondence to Alicia Ponte-Sucre .

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Zerpa, O., Ponte-Sucre, A. (2013). American Tegumentary Leishmaniasis. In: Ponte-Sucre, A., Diaz, E., Padrón-Nieves, M. (eds) Drug Resistance in Leishmania Parasites. Springer, Vienna. https://doi.org/10.1007/978-3-7091-1125-3_10

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  • DOI: https://doi.org/10.1007/978-3-7091-1125-3_10

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