Therapeutic Options for Old World Cutaneous Leishmaniasis and New World Cutaneous and Mucocutaneous Leishmaniasis

被引:37
作者
Monge-Maillo, Begona [1 ]
Lopez-Velez, Rogelio [1 ]
机构
[1] Hosp Ramon & Cajal, IRYCIS, Dept Infect Dis, E-28034 Madrid, Spain
关键词
INTRALESIONAL MEGLUMINE ANTIMONIATE; LIPOSOMAL AMPHOTERICIN-B; RANDOMIZED CLINICAL-TRIAL; SODIUM STIBOGLUCONATE PENTOSTAM; PAROMOMYCIN METHYLBENZETHONIUM CHLORIDE; PLACEBO-CONTROLLED TRIAL; LOCAL HEAT THERAPY; DOUBLE-BLIND; TOPICAL PAROMOMYCIN; MUCOSAL LEISHMANIASIS;
D O I
10.1007/s40265-013-0132-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Estimated worldwide incidence of tegumentary leishmaniasis (cutaneous leishmaniasis [CL] and mucocutaneous leishmaniasis [MCL]) is over 1.5 million cases per year in 82 countries, with 90 % of cases occurring in Afghanistan, Brazil, Iran, Peru, Saudi Arabia and Syria. Current treatments of CL are poorly justified and have sub-optimal effectiveness. Treatment can be based on topical or systemic regimens. These different options must be based on Leishmania species, geographic regions, and clinical presentations. In certain cases of Old World CL (OWCL), lesions can spontaneously heal without any need for therapeutic intervention. Local therapies (thermotherapy, cryotherapy, paromomycin ointment, local infiltration with antimonials) are good options with less systemic toxicity, reserving systemic treatments (azole drugs, miltefosine, antimonials, amphotericin B formulations) mainly for complex cases. The majority of New World CL (NWCL) types require systemic treatment (mainly with pentavalent antimonials), either to speed the healing or to prevent dissemination to oral-nasal mucosa as MCL (NWMCL). These types of lesions are potentially serious and always require systemic-based regimens, mainly antimonials and pentamidine; however, the associated immunotherapy is promising. This paper is an exhaustive review of the published literature on the treatment of OWCL, NWCL and NWMCL, and provides treatment recommendations stratified according to their level of evidence regarding the species of Leishmania implicated and the geographical location of the infection.
引用
收藏
页码:1889 / 1920
页数:32
相关论文
共 180 条
[1]  
Alkhawajah AM, 1997, ANN TROP MED PARASIT, V91, P899, DOI 10.1080/00034989760284
[2]   A 2-year study of liquid nitrogen therapy in cutaneous leishmaniasis [J].
AlMajali, O ;
Routh, HB ;
Abuloham, O ;
Bhowmik, KR ;
Muhsen, M ;
Hebeheba, H .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1997, 36 (06) :460-462
[3]   Fluconazole for the treatment of cutaneous leishmaniasis caused by Leishmania major [J].
Alrajhi, AA ;
Ibrahim, EA ;
De Vol, EB ;
Khairat, M ;
Faris, RM ;
Maguire, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (12) :891-895
[4]   KETOCONAZOLE IN THE TREATMENT OF CUTANEOUS LEISHMANIASIS IN KUWAIT [J].
ALSALEH, QA ;
DVORAK, R ;
NANDA, A .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1995, 34 (07) :495-497
[5]   Leishmaniasis Worldwide and Global Estimates of Its Incidence [J].
Alvar, Jorge ;
Velez, Ivan D. ;
Bern, Caryn ;
Herrero, Merce ;
Desjeux, Philippe ;
Cano, Jorge ;
Jannin, Jean ;
den Boer, Margriet .
PLOS ONE, 2012, 7 (05)
[6]  
Amato V, 1998, ANN DERMATOL VENER, V125, P492
[7]  
Amato V S, 1996, Rev Soc Bras Med Trop, V29, P477, DOI 10.1590/S0037-86821996000500011
[8]  
Amato V S, 2000, Int J Infect Dis, V4, P153, DOI 10.1016/S1201-9712(00)90077-8
[9]   Mucosal leishmaniasis: description of case management approaches and analysis of risk factors for treatment failure in a cohort of 140 patients in Brazil [J].
Amato, V. S. ;
Tuon, F. F. ;
Imamura, R. ;
de Camargo, R. Abegao ;
Duarte, M. I. ;
Neto, V. A. .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2009, 23 (09) :1026-1034
[10]   Short Report: Can We Use a Lower Dose of Liposomal Amphotericin B for the Treatment of Mucosal American Leishmaniasis? [J].
Amato, Valdir S. ;
Tuon, Felipe F. ;
Camargo, Raphael A. ;
Souza, Regina M. ;
Santos, Carolina R. ;
Nicodemo, Antonio C. .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2011, 85 (05) :818-819