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1.
EMHJ-Eastern Mediterranean Health Journal. 2015; 21 (4): 280-286
in English | IMEMR | ID: emr-166763

ABSTRACT

With limited options to treat cutaneous leishmaniasis, constant monitoring of the rate of resistance to pentavalent antimony-based drugs is needed. This study identified the infecting Leishmania species and evaluated the results of meglumine antimoniate [Glucantime[Registered sign]] therapy in a new focus of cutaneous leishmaniasis in Birjand, eastern Islamic Republic of Iran. Smears from 150 patients showed that 141 patients were infected by L. tropica and 9 by L. major. In total, 141 patients with L. tropica infection completed Glucantime[Registered sign] treatment and follow-up; 63.8% were treated intralesionally and 36.2% by intramuscular administration. The overall success rate after one course of therapy with Glucantime[Registered sign] was 96.5% [136/141], and all the failures [5/141] occurred with intramuscular injections. Statistical analysis showed a significant difference between the failure rates of intramuscular and intralesional injections. Children < 10 years old had a significantly higher failure rate than adults


Subject(s)
Humans , Male , Female , Organometallic Compounds , Leishmania tropica , Leishmaniasis, Cutaneous , Treatment Outcome
2.
JMR-Journal of Medical Research. 2004; 2 (4): 1-9
in Persian | IMEMR | ID: emr-66564

ABSTRACT

In Iran, the clinical presentation of cutaneous leishmaniasis is mainly in the form of dry type [urban form] or wet type [rural form]. The microscopic finding of amastigotes in Giemsa-stained smears is the most practical laboratory test for the diagnosis of cutaneous leishmaniasis. However, determination of parasite species is not possible when using this method. Parasite characterization is made by various biochemical, immunological and molecular methods based on massive culture of the parasites. In this study nested PCR was used both for diagnosis as well as species identification. Giemsa-stained slides from forty-nine patients, that had been included in a drug resistance survey, were used in this study. From the available slides, forty-seven were diagnosed as having leishmaniasis using the nested PCR technique. Twenty of these were Leishmania tropica [L. tropica] and the remaining were Leishmania major [L. major]. Amastigotes were recovered from twenty-nine of these patients after standard treatment. This study revealed that clinically drug-resistant cases are more likely to be infected with L. tropica than with L. major, although this difference was not statistically significant. L. tropica was mostly present in facial lesions while L. major was mostly detected in hand and foot lesions. In patients with more than two lesions, L major was the predominant cause. L tropica was the cause of a more prolonged duration of disease. None of the above findings were, however, statistically significant. It can be concluded that nested PCR is a useful technique for studying the molecular epidemiology of leishmaniasis in the field


Subject(s)
Humans , Leishmania/ultrastructure , Polymerase Chain Reaction , Leishmaniasis, Cutaneous/diagnosis , Staining and Labeling , Azure Stains
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