Journal Name:
SKINmed
Volume:
6
Issue:
5
Pages From:
250
To:
252
Date:
الأحد, سبتمبر 9, 2007
Abstract:
In February 2005, a 12-year-old Palestinian Bedouin child with a small lesion on his upper cheek just below the right eye was
referred to Leishmania Research Unit medical laboratory in Jericho for diagnosis of suspected cutaneous leishmaniasis. He lived in
a rocky desert area by Wadi-Qelt, approximately 4 km from Jericho City center and attended the school in the adjacent Aqabat Jabr
refugee camp, which borders Jericho City. He remained confined to this area for the few months before the lesion’s appearance. The
lesion was less than 1 cm in diameter, was bacterially clean, and had a small encrusted crater in its center. The lesion was 2 months
old when first examined. There were no indications of previous cutaneous leishmaniasis, but other family members described
having been exposed to cutaneous leishmaniasis. The family’s residential area was rocky and cavernous with a continuously flowing
stream that provided Jericho with drinking and irrigation water. There were irrigated banana plantations nearby. Extracellular
amastigotes were seen in tissue smears stained with Giemsa stain (Figure 1). These parasites were identified as Leishmania tropica
by DNA analysis. This was done by amplifying the internal transcribed spacer-1 of the ribosomal RNA genes, using a Gene Amp
PCR-system 9700 (Applied Biosystems, Foster City, CA) followed by restriction fragment length polymorphism.1,2 The DNAs of
leishmanial species reference strains were included for comparison (Figure 2). The patient was treated with sodium stibogluconate
injected intralesionally at 10 mg/kg/d every other day for 3 weeks, then twice a week for 2 months, and once a week thereafter for
3 months. The lesion seemed to re-epithelialize during the 3 months from February to early May. The patient was lost to follow-up
until November 2005, when he returned with a small, red, smooth macule. This enlarged, and papules typical of Leishmaniasis
recidivans appeared at its margins. Microscopic examination and DNA analysis were repeated and again showed the presence of
L tropica. The patient was treated with intralesional sodium stibogluconate for another 5 months. The patient returned a third time
in April 2006, 14 months after initial presentation, with a more severe and destructive nodular condition (Figure 3). Microscopic
examination and DNA analysis were repeated, during which 2 tubes of rabbit blood-agar semisolid medium were inoculated with
tissue aspirate to isolate the parasite. This time, no amastigotes were seen in the stained smears, and the internal transcribed spacer-
1-PCR results were negative, but culture medium in 1 tube grew promastigotes. The lesion remained active throughout further
treatment. The Bedouin family said they would apply a traditional therapy.