Identification of from Pediatric Visceral Leishmaniasis in Southern Mediterranean Region of Turkey.

Mediterr J Hematol Infect Dis

Department of Pediatrics, Pediatric Infectious Diseases, Faculty of Medicine, Cukurova University, Adana, Turkey.

Published: July 2022

AI Article Synopsis

  • Protozoa of the genus Leishmania are intracellular parasites that cause different forms of leishmaniasis, with species leading to cutaneous or visceral symptoms.
  • The study aimed to analyze the link between clinical symptoms and molecular characteristics of Leishmania isolates in children with visceral leishmaniasis (VL) in Turkey.
  • Key findings included a high positivity rate for VL in diagnostic tests (93% via microscopy, 79.1% via rK39 test), and the most common symptoms were fever and splenomegaly, with significant complications like thrombocytopenia and hemophagocytic lymphohistiocytosis also observed.

Article Abstract

Background And Objective: Protozoa of the genus are obligate intracellular parasites, and species cause a spectrum of species-specific clinical symptoms known as cutaneous, mucocutaneous, and visceral leishmaniasis. For example, and cause cutaneous leishmaniasis, while and cause visceral leishmaniasis (VL). However, molecular studies in recent years have shown that species cause different clinical symptoms.

Objectives: Our aim was to evaluate the relationship between the clinical and molecular characterization of leishmania isolates in children with VL defined in Turkey, an intercontinental transitional region.

Methods: The clinical diagnosis of VL was confirmed by detecting amastigotes in the bone marrow aspirate and/or the rK39 test and/or molecular methods (genus-specific PCR, Real-Time PCR, ITS1 PCR-RFLP, DNA sequencing).

Results: Most of the VL patients were referred from the districts of Adana (53.3%) and others from neighboring provinces; Hatay (16.6%), Osmaniye (3%), Gaziantep (3%), Adıyaman (3%), and 20% case were Syrian immigrants A clinical diagnosis of VL was confirmed in 30 patients with different diagnostic methods. 93% was found positive with microscopic examination, 79.1% with rK39 dipstick test, and 60% with genus-specific PCR assay in clinical samples. The isolates were identified as (40%), (26.7%), and (23.3%) using Real-Time PCR, ITS1 PCR-RFLP, and DNA sequencing. There was no cutaneous finding in any case in clinical examination.The most common clinical findings were fever (93.3%) and splenomegaly (90%), followed by hepatomegaly (76.6%). The most common laboratory finding was thrombocytopenia (86.6%), followed by anemia (70%). In addition, hemophagocytic lymphohistiocytosis was detected in bone marrow aspiration in two of our patients. Since pentavalent antimony salts treatment initially failed in four patients, it was necessary to switch to Liposomal-Amphotericin B with treatment success.

Conclusions: The presence of in VL patients, despite the absence of cutaneous findings in any of the cases, shows that this strain can cause VL, contrary to conventional knowledge. In the Adana province, where this study was carried out, from CL cases in previous studies should be taken into account, and visceral spread in CL cases and accompanying cutaneous lesions in VL cases should be investigated in detail.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266607PMC
http://dx.doi.org/10.4084/MJHID.2022.053DOI Listing

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