Author/Authors :
Mashayekhi, Vahid Research Center for Skin Diseases and Cutaneous Leishmaniasis - Mashhad University of Medical Sciences, Mashhad , Mahmoudi, Mahmoud Immunology Research Center - Bu-Ali Research Institute - Medical School - Mashhad University of Medical Sciences, Mashhad , Rastin, Maryam Immunology Research Center - Bu-Ali Research Institute - Medical School - Mashhad University of Medical Sciences, Mashhad , Tayebi, Naser Research Center for Skin Diseases and Cutaneous Leishmaniasis - Mashhad University of Medical Sciences, Mashhad , Taheri, Ahmad Reza Research Center for Skin Diseases and Cutaneous Leishmaniasis - Mashhad University of Medical Sciences, Mashhad , Tavakoli, Maryam Research Center for Skin Diseases and Cutaneous Leishmaniasis - Mashhad University of Medical Sciences, Mashhad
Abstract :
Background: Chronic lupoid leishmaniasis (CLL) is a chronic
form of cutaneous leishmaniasis that is usually resistant to anti
leishmania agents and leishmania is not seen in the histologic
sections. We used polymerase chain reaction (PCR) to detect
leishmania DNA in CLL specimens.
Method: This descriptive cross sectional study was done on
20 paraffin embedded specimens of CLL cases referred to the
dermatology clinic of Imam Reza Hospital, Mashhad, Iran.
Patients’ information including age, sex, duration and location of the lesion was obtained and then skin specimens were reviewed histopathologically and assessed for leishmania DNA using PCR.
Result: Eleven male and 9 female patients with a mean age of
17.95 years were included in our study. The mean duration of
lesions was 3.69 years. Most of the lesions (18 of 20 cases) were located on the face and others were on the limbs. Histologic study showed tuberculoid granulomatous inflammation with a variable ratio of histiocytes and lymphocytes without detection of
leishman body. PCR was positive in 12 cases (60% of cases). We could not find any correlation between the results of PCR and sex,age, duration and location of the lesions. Histiocyte- prominent lesions were more prone to be positive on PCR examination but that was not statistically significant.
Conclusion: Despite the very high sensitivity of PCR for the
diagnosis of usual forms of cutaneous leishmaniasis, it fails to
detect leishmania in a remarkable proportion of CLL specimens.