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painless&#44; frequently ulcerated&#44; erythematous plaques with indurated borders&#44; usually on exposed body regions&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">The clinical diagnosis can be confirmed by the demonstration of amastigotes on skin biopsy specimens&#59; by the growth of promastigotes in culture medium or molecular testing performed on skin biopsy samples&#46; Dermatoscopy can be a valuable tool as an adjunctive diagnostic and follow-up non-invasive technique for <span class="elsevierStyleItalic">in vivo</span> observation of infectious lesions&#46; In the particular case of cutaneous leishmaniasis&#44; the most commonly described dermatoscopic signs are diffuse erythema and vascular structures&#59; other features include hyperkeratosis&#44; central erosion or ulceration&#44; &#34;yellow tears&#34; and white starburst-like patterns&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Although up to 50&#37; of cutaneous leishmaniasis lesions are self-limited and self-healing&#44; treatment is generally required in order to reduce the residual scar and to avoid further spread or transmission of the parasite&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In the particular case of cutaneous form&#44; there are two possible therapeutic approaches&#44; systemic or lesion-directed&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Systemic treatment including miltefosine&#44; pentavalent antimonials&#44; liposomal amphotericin B&#44; pentamidine or azole derivatives is usually required when there are multiple &#40;&#62;3&#41;&#44; large &#40;&#62;4<span class="elsevierStyleHsp" style=""></span>cm&#41; or lesions localized in cosmetically sensitive areas&#59; when there is evidence of loco-regional spread &#40;lymphangitis&#41; or if the patient is immunosuppressed&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">There are several treatment options available for solitary lesions of cutaneous leishmaniasis&#44; such as cryotherapy&#44; topical paromomycin&#44; intralesional antimony derivatives and photodynamic therapy&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Variables such as Leishmania species&#44; the clinical presentation&#44; host immunity status and the risk of extra-cutaneous involvement dictate the best treatment option&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">Intralesional antimony derivatives are a safe and effective treatment and represent a viable alternative for patients with few or small lesions and contraindications to systemic treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;9</span></a> It is usually well tolerated and possible side effects are scarring and transient hyperpigmentation&#46; Conversely&#44; the use of photodynamic therapy for the treatment of cutaneous leishmaniasis&#44; is supported by various case reports and case series&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">6&#8211;8</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">The decision to combine both modalities was based on the attempt to minimise the pain associated with the procedure of intralesional administration since only 4 sessions were performed and the theoretical syngergistic effect of two differente mechanisms of action employed&#44; namely&#44; photodynamic therapy relying on systemic immune response and the antimonial derivative with direct parasiticidal effect&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Since a total of 8 sessions would most likely result in lesion clearance using either one of the modalities in monotherapy&#44; the lack of further comparative data imposes a substantial limitation to the rationale used in this study&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">Although more robust studies are still needed in order to determine the real value of combined approaches vs monotherapy and the optimal treatment modalities&#44; photodynamic therapy and intralesional antimonial derivatives represent convenient options in the setting of localized cutaneous infection in immunocompetent hosts especially in aesthetically sensitive areas&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conclusion</span><p id="par0085" class="elsevierStylePara elsevierViewall">Local therapy is desirable for patients with uncomplicated localized cutaneous leishmaniasis&#46; We combined two locally-acting effective agents with good tolerability and low risk of side effects achieving a complete clinical response and a good cosmetic outcome&#46;</p></span></span>"
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Case and Research Letters
Treatment of Localized Cutaneous Leishmaniasis With Intralesional Meglumine Antimoniate and Photodynamic Therapy
Tratamiento de la leishmaniasis localizada mediante el antimoniato de meglumina intralesional y la terapia fotodinámica
A. Costina,
Autor para correspondencia
adelina.costin@hgo.min-saude.pt

Corresponding author.
, F. Bonitoa, J. Alvesa, H. Barreirosb
a Servicio de Dermatología y venereología, Hospital Garcia de Orta, Almada, Portugal
b Consulta privada, Lisboa, Portugal
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asymptomatic&#44; 4<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>2<span class="elsevierStyleHsp" style=""></span>cm large&#44; indurated crusty plaque on his forehead &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; His medical history was unremarkable&#44; except for early latent syphilis treated 1<span class="elsevierStyleHsp" style=""></span>year ago with good serological response&#46; His family history was unremarkable&#46; He denied any prescribed or over-the-counter medication&#46; His immunization status was up-to-date and his social and travel history were significant for a recent travel to Mexico about 5 months ago&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">The skin biopsy revealed a dermal diffuse inflammatory infiltrate composed by lymphocytes and histiocytes&#46; Leishmania amastigotes were identified in the cytoplasm of dermal macrophages&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The physical examination was otherwise normal&#46; Otorhinolaryngologic endoscopy&#44; bone marrow aspirate and abdominal ultrasound were performed to exclude mucous and visceral involvement&#59; a basic blood panel&#44; viral serologies including HIV and HCV disclosed no abnormalities&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Since it was a solitary lesion in a cosmetically-sensitive location&#44; a combined treatment of intralesional meglumine antimoniate and topical photodynamic therapy was started&#46; The protocol consisted of intralesional injection of 1<span class="elsevierStyleHsp" style=""></span>mL of meglumine antimoniate per session followed by photodynamic therapy with topical methylaminolevulinate&#44; a 3<span class="elsevierStyleHsp" style=""></span>-h incubation period and red light irradiation &#40;light emitting diode lamp &#40;Aktilite&#174;&#44; 630<span class="elsevierStyleHsp" style=""></span>nm&#44; 37<span class="elsevierStyleHsp" style=""></span>J&#47;cm<span class="elsevierStyleSup">2</span>&#41; at weekly intervals on alternate weeks&#44; in a total of 8 sessions&#46; Side effects were minimal and included local erythema and a stinging sensation during the irradiation and immediately afterwards&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">At the end of the treatment&#44; the ulcer had given place to an atrophic scar with post-inflammatory hyperpigmentation &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Although the patient denied a confirmatory biopsy&#44; at 12-month follow-up he remains in clinical remission&#44; corroborated by dermatoscopic absence of vascular structures&#44; yellow follicular &#34;tears&#34; or erythema&#44; displaying only a white central atrophic scar&#44; with resolution of peripheral hyperpigmentation&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Discussion</span><p id="par0035" class="elsevierStylePara elsevierViewall">The clinical presentation of cutaneous leishmaniasis consists of single or multiple&#44; painless&#44; frequently ulcerated&#44; erythematous plaques with indurated borders&#44; usually on exposed body regions&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">The clinical diagnosis can be confirmed by the demonstration of amastigotes on skin biopsy specimens&#59; by the growth of promastigotes in culture medium or molecular testing performed on skin biopsy samples&#46; Dermatoscopy can be a valuable tool as an adjunctive diagnostic and follow-up non-invasive technique for <span class="elsevierStyleItalic">in vivo</span> observation of infectious lesions&#46; In the particular case of cutaneous leishmaniasis&#44; the most commonly described dermatoscopic signs are diffuse erythema and vascular structures&#59; other features include hyperkeratosis&#44; central erosion or ulceration&#44; &#34;yellow tears&#34; and white starburst-like patterns&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Although up to 50&#37; of cutaneous leishmaniasis lesions are self-limited and self-healing&#44; treatment is generally required in order to reduce the residual scar and to avoid further spread or transmission of the parasite&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In the particular case of cutaneous form&#44; there are two possible therapeutic approaches&#44; systemic or lesion-directed&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Systemic treatment including miltefosine&#44; pentavalent antimonials&#44; liposomal amphotericin B&#44; pentamidine or azole derivatives is usually required when there are multiple &#40;&#62;3&#41;&#44; large &#40;&#62;4<span class="elsevierStyleHsp" style=""></span>cm&#41; or lesions localized in cosmetically sensitive areas&#59; when there is evidence of loco-regional spread &#40;lymphangitis&#41; or if the patient is immunosuppressed&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">There are several treatment options available for solitary lesions of cutaneous leishmaniasis&#44; such as cryotherapy&#44; topical paromomycin&#44; intralesional antimony derivatives and photodynamic therapy&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Variables such as Leishmania species&#44; the clinical presentation&#44; host immunity status and the risk of extra-cutaneous involvement dictate the best treatment option&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">Intralesional antimony derivatives are a safe and effective treatment and represent a viable alternative for patients with few or small lesions and contraindications to systemic treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;9</span></a> It is usually well tolerated and possible side effects are scarring and transient hyperpigmentation&#46; Conversely&#44; the use of photodynamic therapy for the treatment of cutaneous leishmaniasis&#44; is supported by various case reports and case series&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">6&#8211;8</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">The decision to combine both modalities was based on the attempt to minimise the pain associated with the procedure of intralesional administration since only 4 sessions were performed and the theoretical syngergistic effect of two differente mechanisms of action employed&#44; namely&#44; photodynamic therapy relying on systemic immune response and the antimonial derivative with direct parasiticidal effect&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Since a total of 8 sessions would most likely result in lesion clearance using either one of the modalities in monotherapy&#44; the lack of further comparative data imposes a substantial limitation to the rationale used in this study&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">Although more robust studies are still needed in order to determine the real value of combined approaches vs monotherapy and the optimal treatment modalities&#44; photodynamic therapy and intralesional antimonial derivatives represent convenient options in the setting of localized cutaneous infection in immunocompetent hosts especially in aesthetically sensitive areas&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conclusion</span><p id="par0085" class="elsevierStylePara elsevierViewall">Local therapy is desirable for patients with uncomplicated localized cutaneous leishmaniasis&#46; 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