Case Report: A Case of Visceral Leishmaniasis Misdiagnosed as Brucellosis

Visceral leishmaniasis (VL) is an infectious disease caused by protozoan parasites of the genus <i>Leishmania</i> and transmitted through the bites of infected female sandflies. Due to its nonspecific clinical presentation, VL is prone to misdiagnosis and underdiagnosis. Though rare, VL is endemic in regions of Africa, South America, Asia, and parts of Europe, including the Mediterranean. This report describes a case of VL initially misdiagnosed as brucellosis due to a history of close contact with sheep. The patient tested negative for brucellosis via serum agglutination, blood culture, and bone marrow smear, and showed no improvement with a combination of omadacycline and rifampin therapy. Definitive diagnosis was achieved through metagenomic next-generation sequencing (mNGS) and confirmation with the rk39 antigen test. The patient was successfully treated with amphotericin B cholesterol sulfate complex and recovered fully. This case highlights the need to consider rare pathogens when epidemiological history and clinical response to treatment are incongruent and emphasizes the value of mNGS in timely diagnosis of VL.

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Publication Details

Journal
Infection and Drug Resistance
Published
2025-05-01
DOI
https://doi.org/10.2147/idr.s508319
Primary Topic
Research on Leishmaniasis Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Case Report: A Case of Visceral Leishmaniasis Misdiagnosed as Brucellosis

Yunzhu Mu, Yaqing Li, Xiaoqing Wang, Jianping Xu
Infection and Drug Resistance
Research on Leishmaniasis Studies
article

Case Report: A Case of Visceral Leishmaniasis Misdiagnosed as Brucellosis

Yunzhu Mu, Yaqing Li, Xiaoqing Wang, Jianping Xu
article en

Abstract

Visceral leishmaniasis (VL) is an infectious disease caused by protozoan parasites of the genus <i>Leishmania</i> and transmitted through the bites of infected female sandflies. Due to its nonspecific clinical presentation, VL is prone to misdiagnosis and underdiagnosis. Though rare, VL is endemic in regions of Africa, South America, Asia, and parts of Europe, including the Mediterranean. This report describes a case of VL initially misdiagnosed as brucellosis due to a history of close contact with sheep. The patient tested negative for brucellosis via serum agglutination, blood culture, and bone marrow smear, and showed no improvement with a combination of omadacycline and rifampin therapy. Definitive diagnosis was achieved through metagenomic next-generation sequencing (mNGS) and confirmation with the rk39 antigen test. The patient was successfully treated with amphotericin B cholesterol sulfate complex and recovered fully. This case highlights the need to consider rare pathogens when epidemiological history and clinical response to treatment are incongruent and emphasizes the value of mNGS in timely diagnosis of VL.

Infection and Drug ResistanceVol. Volume 18
Hebei North University (CN), Hebei General Hospital (CN)
Openalex Percentile: Top 84%
Research on Leishmaniasis Studies
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