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Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...
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Cutaneous Leishmaniasis in the Dorsal Skin of Hamsters: a Useful Model for the Screening of Antileishmanial Drugs
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Published on: April 21, 2012

[Cutaneous leishmaniasis--an import from Belize].

Jakob Schnedl1, Herbert Auer, Marcellus Fischer

  • 1Heeresspital Wien, Dermatologische Abteilung, Wien, Osterreich. jakob.schnedl@meduniwien.ac.at

Wiener Klinische Wochenschrift
|December 6, 2007
PubMed
Summary

New World cutaneous leishmaniasis, potentially caused by Leishmania (Viannia) braziliensis, requires systemic treatment due to dissemination risk. Intravenous pentamidine effectively treated three soldiers with ulcers acquired in Belize.

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Area of Science:

  • Tropical medicine
  • Parasitology
  • Dermatology

Background:

  • Cutaneous leishmaniasis (CL) in the New World, especially from Leishmania (L.) braziliensis, poses a risk of dissemination.
  • Disseminated CL can lead to mucocutaneous leishmaniasis, causing severe orofacial destruction, even years after initial skin lesion resolution.
  • Old World CL is typically localized, allowing for conservative management.

Observation:

  • Three Austrian soldiers presented with multiple upper limb ulcers weeks after a jungle patrol course in Belize.
  • Diagnosis was confirmed via histological evaluation of biopsies and detection of amastigote Leishmania in ulcer smears.
  • Species identification was not performed, necessitating consideration of L. brasiliensis and potential mucocutaneous progression.

Findings:

  • Initial treatments including cryotherapy, topical paromomycin, and oral fluconazole were ineffective.
  • Systemic therapy with intravenous pentamidine (3-4 mg/kg, three doses) resulted in complete regression of lesions within four weeks.

Implications:

  • Systemic treatment is crucial for New World CL when L. (Viannia) braziliensis infection is suspected.
  • Intravenous pentamidine demonstrates efficacy in treating severe or treatment-refractory cutaneous leishmaniasis.
  • Prompt and appropriate systemic therapy can prevent severe disease progression and complications.