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Notes:
conferenceseries
.com
November 28-29, 2016 Valencia, Spain
4
th
World Congress on
Infection Prevention and Control
Volume 4, Issue 8 (Suppl)
J Infect Dis Ther 2016
ISSN: 2332-0877, JIDT an open access journal
Infection Control 2016
November 28-29, 2016
The first report of visceral leishmaniasis caused by
Leishmania major
in Iran
Bibi Razieh Hosseini Farash
Tehran University of Medical Sciences, Iran
Purpose:
In Iran, HIV/AIDS is an emerging disease and both Visceral Leishmaniasis (VL) and HIV infections occur sporadically.
The known causative agent in Iran for VL is
Leishmania infantum
which is endemic in Ardabil and Fars Provinces. The aim of this
study is to report of VL caused by
Leishmania major
in an AIDS patient.
Methods:
Direct agglutination test (DAT) was performed on a 53 year old HIV/infected male with chronic intermittent diarrhea who
registered in AIDS center of Khorasan Razavi Province to investigate VL/HIV co infection. The mean of CD4+ was 79/mm
3
in this
patient. The DAT result was confirmed by bone marrow aspiration and polymerase chain reaction (PCR).
Results:
DAT test was positive with titer 1:25,600. The amastigote forms of
Leishmania
sp. were found in bone marrow aspiration
materials and
L. major
was identified by nested PCR assay compared to standard pattern.
Conclusions:
Based on the DAT and PCR results for VL, it is recommended that a high sensitive serological test should be
performed on HIV positive patients, especially in where are endemic for VL. Other
Leishmania
sp. could be causative agents for VL
in immunocompromised people; therefore the observed amastigotes in bone marrow aspiration should be examined by molecular
methods to identify
Leishmania
sp. VL/HIV co-infection can occur in endemic areas for cutaneous leishmaniasis, so some studies are
proposed to investigate VL caused by CL causative agents in HIV patients.
Biography
Bibi Razieh Hosseini Farash is affiliated to the Tehran University of Medical Sciences, Iran.
raziehhoseinifr@yahoo.comBibi Razieh Hosseini Farash, J Infect Dis Ther 2016, 4:8 (Suppl)
http://dx.doi.org/10.4172/2332-0877.C1.020