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Treating pediatric cutaneous Leishmania tropica with systemic liposomal amphotericin B: A retrospective, single-center study.
Noyman, Yehonatan; Levi, Assi; Ben Amitai, Dan; Reiss-Huss, Shiran; Sabbah, Fareed; Hodak, Emmilia; Mimouni, Tomer; Friedland, Rivka.
Affiliation
  • Noyman Y; Division of Dermatology, Rabin Medical Center, Petah Tikva, Israel.
  • Levi A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Ben Amitai D; Division of Dermatology, Rabin Medical Center, Petah Tikva, Israel.
  • Reiss-Huss S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Sabbah F; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Hodak E; Pediatric Dermatology Unit, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Mimouni T; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Friedland R; Pediatric Dermatology Unit, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
Dermatol Ther ; 35(1): e15185, 2022 01.
Article in En | MEDLINE | ID: mdl-34716724
ABSTRACT
Leishmania tropica (L. tropica) cutaneous leishmaniasis (CL) is associated with high morbidity and low response rate to therapy, especially in pediatric patients. Intravenous (IV) liposomal amphotericin B (LAmB) has been used off-label as a treatment for L. tropica CL for many years. However, data regarding its efficacy and safety in children is lacking. In order to evaluate the efficacy and safety of IV LAmB for treating pediatric patients with L. tropica, we retrospectively reviewed electronic medical records of 24 children who were diagnosed with L. tropica CL and treated with IV LAmB during 2014-2020, at a tertiary medical center in Israel. Fourteen (58%) completed the treatment protocol and 10 (42%) experienced an infusion-related adverse event (IRAE) leading to treatment termination. Complete response was noted in 6/14 (43%) patients, while 8/14 (57%) failed to respond. Lower response rate was noted in lesions involving the mid-facial area. The relatively low response rate is speculated to result from a low dose of LAmB, short follow-up period, and difficult to treat anatomic locations. The observation of a lower response rate for mid-facial lesions should be validated in larger cohorts. The highrisk of IRAE should be considered in physician decisions regarding this treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leishmania tropica / Leishmaniasis, Cutaneous Type of study: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Dermatol Ther Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: Israel

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leishmania tropica / Leishmaniasis, Cutaneous Type of study: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Dermatol Ther Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: Israel