Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/34855
Наслов: Visceral Leishmaniasis in the Republic of North Macedonia: A Retrospective Cohort Study
Authors: Bosilkovski, Mile 
Khezzani, Bachir
Cana, Fadil
Poposki, Kostadin 
Jakimovski, Dejan 
Nikolic, Jadranka
Georgievska, Dajana
Dimzova, Marija 
Keywords: Visceral leishmaniasis
fever
splenomegaly
cytopenia
treatment
Issue Date: 11-ное-2025
Publisher: Galenos Yayinevi
Journal: Mediterranean Journal of Infection Microbes and Antimicrobials
Abstract: Visceral leishmaniasis (VL) is a systemic protozoan vector-borne disease and represents the most severe clinical form of leishmaniasis, with fatal outcomes if left untreated. This study aimed to evaluate the key epidemiological, clinical, and laboratory findings, treatment options, and outcomes in patients with VL. Materials and Methods A retrospective analysis was conducted on the epidemiological and clinical characteristics of 84 patients diagnosed and treated for VL at the University Hospital for Infectious Diseases in Skopje, Republic of North Macedonia (RNM), between 2001 and 2023. Results The median age of patients was 47 years (range 1-74), with 77.4% being male. Contact with dogs was reported in 41.7% of cases. Seven percent of patients were immunosuppressed, and all were Human Immunodeficiency Virus-negative. The median time from symptom onset to diagnosis was 30 days (range 4-330 days). The predominant clinical manifestations were splenomegaly (97.6%), fever (96.4%), hepatomegaly (90.5%), and weight loss (54.8%). On admission, anemia, leukopenia, thrombocytopenia, and hypergammaglobulinemia were detected in 75%, 73.8%, 70.2%, and 63.1% of patients, respectively. A favorable outcome was achieved in 91.7% of cases; therapeutic failure occurred in 1.2%, and 7.1% of patients died. Conclusion VL should be considered a crucial differential diagnosis in patients from the RNM presenting with prolonged unexplained fever, splenomegaly, cytopenia, and hypergammaglobulinemia.
URI: http://hdl.handle.net/20.500.12188/34855
DOI: 10.4274/mjima.galenos.2025.25453.18
Appears in Collections:Faculty of Medicine: Journal Articles

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