What is the treatment for cutaneous leishmaniasis?

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Treatment of Cutaneous Leishmaniasis

For simple, localized cutaneous leishmaniasis lesions (small, recent-onset, uncomplicated), local therapy with intralesional pentavalent antimonials, heat therapy, or cryotherapy should be the preferred first-line approach, while complex cases (multiple lesions, lesions >4cm, facial/joint involvement, or species with mucosal risk) require systemic therapy with liposomal amphotericin B, pentavalent antimonials, or miltefosine. 1

Treatment Selection Algorithm

Step 1: Classify the Lesion as Simple vs. Complex

Simple CL (suitable for local therapy): 1

  • Small lesions (<30mm width)
  • Single or few lesions
  • Recent onset (<3 months)
  • Non-ulcerative or small ulcerative forms
  • NOT on eyelids, lips, nose, ears, or fingers
  • No evidence of dissemination (no subcutaneous nodules or regional adenopathy)
  • NOT caused by New World species with mucosal risk (L. braziliensis, L. panamensis, L. guyanensis)

Complex CL (requires systemic therapy): 1

  • Multiple lesions or large lesions (>4cm)
  • Lesions on face, joints, or near mucosal areas
  • Evidence of lymphatic spread
  • Caused by species with mucosal leishmaniasis risk
  • Immunocompromised patients
  • Lesions present >6 months

Step 2: Local Therapy Options for Simple CL

Intralesional Pentavalent Antimonials (First Choice for Simple OWCL): 1

  • Use undiluted sodium stibogluconate or meglumine antimoniate
  • Dose: 0.1 mL/cm² injected intradermally with 25-27G needle
  • Volume: 0.2-5 mL per session at up to 4-5 injection sites
  • Frequency: Every 3-7 days for 5-8 sessions until healing
  • Pre-medicate with EMLA cream (lidocaine/prilocaine) for pain control
  • Avoid on fingers, nose, ears, eyelids, near lips, or areas of vascular concern
  • Success rates: 89-91% when combined with cryotherapy 1

Cryotherapy (Especially Effective When Combined with IL Antimonials): 1

  • Apply liquid nitrogen for 15-20 seconds until 1-2mm of surrounding skin frozen
  • Thaw 20-60 seconds, then repeat freeze
  • Repeat entire process every 3 weeks for up to 3 applications
  • When combined with intralesional antimonials: use shorter application (no second freeze), allow skin to normalize, then inject antimonials
  • Best for lesions <30mm, on face/neck, dry, present <3 months
  • Avoid eyelids, lips, nose, ears
  • Safe in pregnancy and breastfeeding 1

Heat Therapy (ThermoMed Device): 1

  • Apply at 50°C for 30-second doses in grid pattern
  • Extend 1-2mm into normal-appearing skin
  • Usually one session (sometimes up to 3)
  • Use topical antibiotics for several days post-treatment
  • Avoid same anatomical sites as cryotherapy
  • FDA-cleared for CL indication 1

Topical Paromomycin: 1

  • 15% paromomycin + 12% MBCL ointment: apply BID for 10 days, rest 10 days, reapply BID for 10 days
  • OR 15% paromomycin + 0.5% gentamicin cream: apply once daily for 20 days
  • Higher response rates for L. major than L. tropica 1

Step 3: Systemic Therapy Options for Complex CL

Liposomal Amphotericin B (Preferred for Species with Mucosal Risk): 2

  • Dose varies by species and geography; typically 3 mg/kg/day
  • Less toxic than conventional amphotericin B deoxycholate
  • Particularly important for L. braziliensis, L. panamensis, L. guyanensis 2

Pentavalent Antimonials (Sodium Stibogluconate or Meglumine Antimoniate): 1, 2, 3

  • Dose: 20 mg SbV/kg/day IV or IM for 20 days (cutaneous) or 28 days (mucosal)
  • No upper limit on daily dose (remove the 850mg cap) 3
  • Efficacy: 62-95% for cutaneous leishmaniasis 4, 5
  • Alternative regimen: 5 mg SbV/kg/day IM for 30 days (less toxic, 84% efficacy) 4
  • Requires laboratory monitoring (hepatic, renal, cardiac function)
  • Both sodium stibogluconate and meglumine antimoniate show similar efficacy 5

Miltefosine (Only Oral Option): 1, 6

  • FDA-approved for CL due to L. braziliensis, L. guyanensis, L. panamensis
  • Dose: If 30-44 kg: 50mg BID for 28 days; if ≥45 kg: 50mg TID for 28 days
  • Target dose: ~2.5 mg/kg/day
  • Efficacy: 66% overall (82% for L. braziliensis in Colombia, 48% in Guatemala, 67.5-85% in Brazil) 6
  • Good evidence for Old World CL; variable results for New World CL depending on species and geography 1
  • Contraindicated in pregnancy (teratogenic); requires effective contraception during and 2 months post-therapy 6

Critical Pitfalls to Avoid

Do NOT use local therapy alone for: 1

  • New World CL species that can cause mucosal leishmaniasis (L. braziliensis, L. panamensis, L. guyanensis)
  • Patients with evidence of dissemination (subcutaneous nodules, regional adenopathy)
  • Lesions on high-risk anatomical sites (eyelids, lips, nose, ears, fingers)

Do NOT switch to amphotericin B deoxycholate if patient has toxicity with liposomal amphotericin B, as conventional formulation is almost always more toxic 2

Debride eschar overlying ulcers before local therapy and manage secondary infection to maximize treatment effect 1

Monitoring Treatment Response

Clinical criteria (not parasitologic testing): 1, 2

  • Lesion flattening and >50% size decrease by 4-6 weeks
  • Re-epithelialization of ulcerative lesions by approximately 3 months
  • Healing may continue after treatment completion, especially for large ulcers
  • Monitor for 6-12 months post-treatment for relapse

Mucosal surveillance: 1

  • Perform careful nasal and oropharyngeal examination periodically up to 1-2 years
  • Educate patients about signs of mucosal involvement (nasal stuffiness, epistaxis, hoarseness)
  • Any suspicious symptoms warrant fiber-optic examination

Special Populations

Pregnancy/Breastfeeding: 1

  • Cryotherapy is safe
  • Avoid miltefosine (teratogenic)
  • Pentavalent antimonials have limited safety data

Immunocompromised: 1

  • Always use systemic therapy
  • Higher risk of dissemination
  • May require combination therapy or higher doses

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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