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SYMPOSIUM - LIESHMANIASIS Table of Contents   
Year : 2010  |  Volume : 2  |  Issue : 2  |  Page : 147-150
Treatment strategies for mucocutaneous leishmaniasis


Department of Pediatric, Hospital of Sondrio, Italy

Click here for correspondence address and email

Date of Web Publication30-Apr-2010
 

   Abstract 

Mucocutaneous is an infection caused by a single celled parasite transmitted by sand fly bites. There are about 20 species of Leishmania that may cause mucocutaneous leishmaniasis. Some Leishmania species are closely linked to humans and are therefore found in cities (L. tropica) whereas some others are more traditionally associated with animal species and therefore considered zoonoses (L. major). The evidence for optimal treatment of mucocutaneous leishmaniasis is patchy. Although the cutaneous form of the disease is often self-limiting, it does result in significant scarring and can spread to more invasive, mucocutaneous disease. Therefore, treatment may be considered to prevent these complications. Drugs for systemic and topical treatment are presented and discussed with regard to their application, use and adverse effects.

Keywords: Cutaneous leishmaniasis, Paromomycin, Pentavalent antimonials, Treatment

How to cite this article:
Palumbo E. Treatment strategies for mucocutaneous leishmaniasis. J Global Infect Dis 2010;2:147-50

How to cite this URL:
Palumbo E. Treatment strategies for mucocutaneous leishmaniasis. J Global Infect Dis [serial online] 2010 [cited 2014 Nov 27];2:147-50. Available from: http://www.jgid.org/text.asp?2010/2/2/147/62879



   Introduction Top


The distribution of mucocutaneous leishmaniasis is very tightly linked to geography and villages even 15 miles apart can have very different rates of cutaneous leishmaniasis. There are about 20 species of Leishmania that may cause these diseases. Some Leishmania species are closely linked to humans and are therefore found in cities (L. tropica) some others are more traditionally associated with animal species and therefore considered zoonoses (L. major). Some species that are traditionally considered zoonotic (e.g. L. panamensis) becoming primarily human diseases of leishmania are transmitted to human skin by the bite of a sand fly. Leishmania invades human macrophages and replicates intracellularly. A raised, red lesion develops at the site of the bite (often weeks or sometimes years afterwards). The lesion then ulcerates and may become secondarily infected with bacteria. In many species (for example, L. major) the lesion often spontaneously heals with atrophic scarring. In some species (for example, L. viannia braziliensis) the lesion may spontaneously heal with scarring, but re-appear elsewhere as destructive mucocutaneous lesions. Lesions of other leishmania species may spontaneously heal and then re-appear as satellite lesions around the site of the original lesion, or along the route of lymphatic drainage. Some species tend to cause cutaneous and mucocutaneous leishmaniasis (L. major and L. tropica), whereas some species tend to cause visceral leishmaniasis (L. infantum and L donovani.[1],[2],[3] Diagnosis is based on the characteristic appearance of non-healing raised, scaling lesions that may ulcerate and become secondarily infected with organisms such as Staphylococcus aureus, in someone who has returned from an endemic area. The gold standard for diagnosis is PCR. [4] The evidence for optimal treatment of muco-cutaneous leishmaniasis is patchy. Although the cutaneous form of the disease is often self-limiting, it does result in significant scarring and can spread to more invasive, mucocutaneous disease. Therefore, treatment may be considered to prevent these complications. [5]


   Treatment Strategies Top


Drugs for systemic and topical treatment are presented and discussed with regard to their application, use and adverse effects.

Systemic treatment

The pentavalent antimonials are considered the gold standard for treatment of leishmaniasis. Two preparations are currently available abroad: sodium stibogluconate (Pentostam, GlaxoSmithKline) for intravenous and intramuscular administration and meglumine antimoniate (Glucantime, Specia Rhone Poulenc) for intramuscular administration. The biochemical basis for their effectiveness is unknown, but may involve inhibition of ATP synthesis. The drugs exist only in parenteral forms. The dosage is usually given in Sb equivalents (mg/kg/day). The pentavalent antimonials are far from ideal drugs because of their difficult administration and toxicity. [6],[7] The adverse effects of the drug can also be significant and include pancreatitis, hepatitis, marrow suppression and changes to the electrocardiograph (QT prolongation). Other common adverse effects include myalgias, fatigue, headache, rash and nausea. In most instances, these events resolve when therapy is discontinued, and, therefore, weekly monitoring is recommended to rapidly detect toxicities and address them as they occur. Treatment schedules and dosages have been debated and changed several times. In the 1980s, the dosage was increased from 10 to 20 mg/kg/day, with an upper limit of 850 mg/day (equivalent to two ampoules of meglumine antimonate). The upper limit of 850 mg Sb/day was abandoned in the early 1990s, since studies indicated a reduced efficacy of lower doses and no higher toxicity was found with the higher doses of the drug. [8] Pentamidine, an aromatic diamidine, is toxic for a number of protozoa and fungi including Leishmania, Pneumocystis carinii and African trypanosomes. The mechanism of action has not been established. Pentamidine is used as an alternative to the pentavalent antimonials, and is the first line treatment for cutaneous leishmaniasis in French Guyana, where L. guyanensis is responsible for >90% of the cases. [9],[10] A study in Colombia (with L. panamensis, L. brasiliensis and L. mexicana) found that a short-course, low-dose regimen of pentamidine isethionate had a similar cure rate (96%) to that of meglumine antimonate (91%), with similar rates of side effects. [11] The short-course, low-dosage regimen of pentamidine in otherwise healthy patients with cutaneous leishmaniasis was better tolerated than the higher dosages applied for Pneumocystis treatment in HIV-positive patients: all adverse effects were reversible and no cases of new diabetes mellitus were found among >2200 patients observed with the low-dose regimen. However, the higher dosages needed for the treatment of mucosal leishmaniasis (>2000 mg) may cause diabetes mellitus. [12] Blood sugar and glycemia need to be checked before every injection, because reversible glucosuria and hyperglycemia have been described. [13] Other side-effects are: nephrotoxicity (asymptomatic azotemia to renal failure), hypotension and arrhythmias, nausea, vomiting and diarrhea, leucopenia, anemia and thrombocytopenia, cough and bronchospasm, acute hepatitis and neurological alterations as neuralgia, confusion and hallucinations. The imidazoles and the structurally related triazoles were introduced as antifungal drugs, but also have an antileishmanial activity. They have the advantage of oral administration and few adverse effects, but are only effective against some species (see species-specific treatment below). Fluconazole was studied in a randomized, double-blind, placebo-controlled trial in Iran. [14] It was well tolerated and showed promising results in Leishmania major leishmaniasis. In a recent study a total of 106 patients were assigned to receive fluconazole, and 103 patients were assigned to receive placebo. Follow-up data were available for 80 and 65 patients, respectively. At the three-month follow-up, healing of lesions was complete for 63 of the 80 patients in the fluconazole group (79%) and 22 of the 65 patients in the placebo group (34%). According to an intention-to-treat analysis, the rates of healing were 59 and 22%, respectively. Sodium stibogluconate was offered to 11 patients in the fluconazole group who returned for follow-up and 33 of those in the placebo group (51%) in whom oral treatment was judged to have failed. Side effects were mild and similar in both groups. This study evidences as a six-week course of oral fluconazole is a safe and useful treatment for mucocutaneous leishmaniasis caused by L. major. Nausea, vomiting, diarrhea, stomach upset/pain, headache, dizziness, or hair loss may occur during treatment with fluconazole. This drug may rarely cause serious (possibly fatal) liver disease. A serious allergic reaction to this drug is unlikely, but seeks immediate medical attention if it occurs. Symptoms of a serious allergic reaction include: rash, itching, swelling, severe dizziness, trouble breathing. Miltefosine, a recent phosphocholine analogue, showed high in vitro activity against leishmania. Using doses of 133-150 mg/day for three to four weeks, the per protocol cure rate (no parasites after therapy, complete re-epithelialization after three months) was 94%. However, a longer follow-up is needed to evaluate the relapse rate. The most common side-effects were motion sickness, gastrointestinal complaints, headache and raised liver enzymes. [15] It has exhibited teratogenicity and should not be administered to pregnant women. The antifungal agent amphotericin B desoxycholate is active against Leishmania species, but has the disadvantage of a high incidence of adverse reactions (hyperpyrexia, severe malaise, hypotension, thrombophlebitis, azotaemia, renal tubular damage, hypokalemia, anemia and hepatitis). Based on currently available data, liposomal amphotericin B has been insufficiently studied with regard to formulation and dosage to assess its efficacy in mucocutaneous leishmaniasis. Allopurinol, an analogue of hypoxanthine, is generally not effective in the absence of pentavalent antimony. [16] Two azole antifungal agents, itraconazole and ketoconazole, have been used to treat mucocutaneous disease. Ketoconazole, which has the broadest spectrum, is unfortunately very poorly tolerated. Therapy-limiting adverse events include gastrointestinal symptoms (nausea, vomiting) as well as hepatotoxicity. Itraconazole, although better tolerated than ketoconazole, is associated with more treatment failures than the other azole compound.


   Local Treatment Top


Topical therapies to treat cutaneous leishmaniasis include both pharmacologic and non-drug modalities. Non-drug therapy including cauterization, surgical excision, cryotherapy, but the simplest of these treatments is the local application of heat. As Leishmania species are heat labile, this topical therapy has been proven effective in placebo-controlled studies. There is an FDA-approved device (that treats cutaneous disease. This radio-frequency heat generator can be used either as a single treatment or as part of a multiple treatment course. Cryotherapy is the most common and it is performed by repeated topical applications of liquid nitrogen with a cotton-tipped applicator or a cotton swab with moderate pressure to the lesion, up to 2 mm outside the lesion margin. The freezing time per application is 15-20 second. The procedure is repeated two or three times at short intervals, resulting in a total time of 30-120 second. Adequate application is reflected in the whitening of the skin at 2-3 mm outside the margins of the lesion. In an non-randomized study from Turkey, the cure rates (complete healing and disappearance of all clinical features) after one or two sessions of cryotherapy were 77% (46/60) after one month and 73% (44/60) after three months, compared with 85% after 1 and 3 months following intralesional sodium stibogluconate. [17] Paromomycin, an aminoglycoside antibiotic (identical to aminosidine) has been used systemically against both visceral and cutaneous leishmaniasis. As an ointment for topical use, it has been tested in different formulations, either with methylbenzethonium in white soft paraffin, or with urea and white soft paraffin. The combination of paromomycin with methylbenzethonium appears to be more effective than the combination with urea, but it causes more local inflammatory reactions. [18] With New World leishmaniasis, however, experts are hesitant to treat cutaneous lesions topically because of the risk of mucosal disease, although this ointment was reported to have much better cure rates than placebo in two studies. [19],[20] Local infiltration with pentavalent antimonial is an other therapeutic option. Local infiltration of lesions with pentavalent antimony produces the maximum concentration in the lesions and has few systemic side effects, but does not reach metastatic infections. The basic aim is to fill the infected part of the dermis with pentavalent antimony. This means carefully infiltrating the area around the lesion, including the base of the lesion. A fine gauge (25G) needle is used to inject the drug under pressure as the needle advances. Injection into the dermis is difficult, as the tissue space is small. The drug must not be injected into the subcutaneous tissue, where it is rapidly absorbed and does not reach the site of infection. In an Iranian study 96 patients with clinical and parasitological diagnosis of cutaneous leishmaniasis were recruited to a comparative randomized clinical trial to evaluate the efficacy of topical paromomycin vs. weekly intralesional injections of meglumine antimoniate. The patients were randomly divided into two treatment groups: one group was treated with topical paromomycin ointment and the other with intralesional meglumine antimoniate. Treatment was continued in both groups until complete recovery occurred (defined as healing in less than two months with no residual scar or relapse for up to one year post-treatment). Treatment failure was defined as an increase in the number and size of pre-existing lesions or untoward side-effects. The maximum treatment period was three months. The patients were followed up for one year. The results showed that intralesional meglumine antimoniate led to 41.7% complete recovery. However, topical paromomycin gave a lower cure rate of 16.6%. Treatment failure was observed in 39.7% of the group receiving intralesional meglumine and in 72.9% of those on topical paromomycin. This study indicates that intralesional meglumine antimoniate is superior to topical paromomycin in the treatment of cutaneous leishmaniasis. [21] Other topical creams that produce nitric oxide may also be beneficial for cutaneous leishmaniasis. These include SNAP (S-nitroso-N-acetylpenicillamine), ascorbic acid, salicylic acid and nitrite creams. Studies with each of these agents have had variable results. It does appear that the vehicle plays an important role in the effectiveness of topical treatments. Further studies are needed to determine their exact role in therapy.


   Conclusion Top


The pentavalent antimonials are considered the gold standard for treatment of leishmaniasis but the adverse effects of the drug can also be significant and include pancreatitis, hepatitis, marrow suppression and changes to the electrocardiograph. Also pentamidine is efficient but with many side effects as diabetes mellitus, nephrotoxicity, and anemia. The antifungal agent amphotericin B desoxycholate is active against Leishmania species, but has the disadvantage of a high incidence of adverse reactions. Itraconazolo and ketoconazole are generally well tolerated, but your use is limited by the fact that they demonstrate a slower activity against a limited number of strains. Flucanozole and miltefosine are generally well tolerated but other studies are needed to evaluate your efficacy. In consideration of toxicities of many drugs the selection of the therapeutic agent depends on the potential benefit of treatment versus the significant toxicities of many of these therapies.

 
   References Top

1.Herwaldt BL. Leishmaniasis. Lancet 1999;354:1191-9.  Back to cited text no. 1      
2.Hyams KC, Hanson K, Wignall FS, Escamilla J. The impact of infectious diseases on the health of U.S. troops deployed to the Persian Gulf during operations Desert Shield and Desert Storm. Clin Infect Dis 1995;20: 1497-504.  Back to cited text no. 2      
3.Desjeux P. Worldwide increasing risk factors for leishmaniasis. Med Microbiol Immunol 2001;190:77-9.  Back to cited text no. 3      
4.Murray HW, Berman J, Davies CR, Saravia NG. Advances in leishmaniasis. Lancet 2005;366:1561-77.  Back to cited text no. 4      
5.Blum J, Desjeux P, Schwartz E, Beck B, Hatz C. Treatment of cutaneous leishmaniasis among travellers. J Antimicrob Chemother 2004;53:158-66.   Back to cited text no. 5      
6.Herwaldt B, Berman D. Recommendations for treating leishmaniasis with sodium stibogluconate (Pentostam) and review of pertinent clinical studies. Am J Trop Med Hyg 1992;46:296-306.  Back to cited text no. 6      
7.Esfandiarpour I, Alavi A. Evaluating the efficacy of allopurinol and meglumine antimoniate (Glucantime) in the treatment of cutaneous leishmaniasis. Int J Dermatol 2002;41:521-4.  Back to cited text no. 7      
8.Wortmann G, Miller RS, Oster C, Jackson J, Aronson N. A randomized, double-blind study of the efficacy of a 10- or 20-day course of sodium stibogluconate for treatment of cutaneous leishmaniasis in United States military personnel. Clin Infect Dis 2002;35:261-7.  Back to cited text no. 8      
9.Nacher M, Carme B, Sainte Marie D, Couppiι P, Clyti E, Guibert P, et al. Influence of clinical presentation on the efficacy of a short course of pentamidine in the treatment of cutaneous leishmaniasis in French Guiana. Ann Trop Med Parasitol 2001;95:331-6.  Back to cited text no. 9      
10.Pradinaud R. Le traitement de la leishmaniose tιgumentaire par la pentamidine en Guyane franηaise. Med Trop 1994;54:418-22.  Back to cited text no. 10      
11.Soto J, Buffet P, Grogl M, Berman J. Successful treatment of Colombian cutaneous leishmaniasis with four injections of pentamidine. Am J Trop Med Hyg 1994;50:107-11.  Back to cited text no. 11      
12.Amato V, Amato J, Nicodemo A, Uip D, Amato-Neto V, Duarte M. Treatment of mucocutaneous leishmaniasis with pentamidine isothionate. Ann Dermatolol Venereol 1998;125:492-5.  Back to cited text no. 12      
13.Soto-Mancipe J, Grogl M, Berman JD. Evaluation of pentamidine for the treatment of cutaneous leishmaniasis in Colombia. Clin Infect Dis 1993;16:417-25.  Back to cited text no. 13      
14.Alrajhi AA, Ibrahim EA, De Vol EB, Khairat M, Faris RM, Maguire JH. Fluconazole for the treatment of cutaneous leishmaniasis caused by Leishmania major. N Engl J Med 2002;346:891-5.  Back to cited text no. 14      
15.Soto J, Toledo J, Gutierrez P, Nicholls RS, Padilla J, Engel J, et al. Treatment of American cutaneous leishmaniasis with miltefosine, an oral agent. Clin Infect Dis 2001;33:E57-61.  Back to cited text no. 15      
16.D'Oliveira JA, Machado PR, Carvalho EM. Evaluating the efficacy of allopurinol for the treatment of cutaneous leishmaniasis. Int J Dermatol 1997;36:938-40.  Back to cited text no. 16      
17.Gurei MS, Tatli N, Ozbilge H, Erel O, Seyrek A, Kocyigit A, et al. Efficacy of cryotherapy and intralesional pentostam in treatment of cutaneous leishmaniasis. J Egypt Soc Parasitol 2000;30:169-76.  Back to cited text no. 17      
18.Bryceson AD, Murphy A, Moody AH. Treatment of 'Old World' cutaneous leishmaniasis with aminosidine ointment: results of an open study in London. Trans R Soc Trop Med Hyg 1994;88:226-8.  Back to cited text no. 18      
19.Arana BA, Mendoza CE, Rizzo NR, Kroeger A. Randomized, controlled, double-blind trial of topical treatment of cutaneous leishmaniasis with paromomycin plus methylbenzethonium chloride ointment in Guatemala. Am J Trop Med Hyg 2001;65:466-70.  Back to cited text no. 19      
20.Krause G, Kroeger A. Topical treatment of American cutaneous leishmaniasis with paramomycin and methylbenzethonium chloride: a clinical study under field conditions in Ecuador. Trans R Soc Trop Med Hyg 1994;88:92-4.  Back to cited text no. 20      
21.Faghihi G, Tavakoli-Kia R. Treatment of cutaneous leishmaniasis with either topical paramomycin or intralesional meglumine antimoniate. Clin Exp Dermatol 2003;28:13-6.  Back to cited text no. 21      

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Correspondence Address:
Emilio Palumbo
Department of Pediatric, Hospital of Sondrio
Italy
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DOI: 10.4103/0974-777X.62879

PMID: 20606970

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    Abstract
    Introduction
    Treatment Strategies
    Local Treatment
    Conclusion
    References

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