# Trends in Leishmaniasis: A 32-Year Review in an Endemic Area in the South of Madrid Region

**Authors:** Víctor Antón-Berenguer, Óscar Manuel Muñoz Clemente, Beatriz López Quintana, Belén Martínez Mondéjar, Sara Moreno-García, Montserrat Chao Crecente, José Miguel Rubio Muñoz, Francisco Jesús Merino Fernández, Carmen Chicharro Gonzalo, Emilia García Díez, Francisco Javier Nieto Martínez, María Delmans Flores-Chávez

PMC · DOI: 10.3390/pathogens15020127 · 2026-01-24

## TL;DR

This study reviews 32 years of leishmaniasis cases in an endemic area of Madrid, showing changes in patient demographics, diagnosis, and treatment over time.

## Contribution

The study provides a long-term analysis of leishmaniasis trends in a specific endemic region, including shifts in patient groups and medical practices.

## Key findings

- Visceral leishmaniasis (VL) shifted from affecting HIV patients to elderly and non-HIV immunosuppressed individuals.
- Diagnostic methods evolved from microscopy to molecular and chemiluminescence assays.
- Amphotericin B became the preferred treatment for VL over meglumine antimoniate.

## Abstract

In Spain, Leishmania infantum causes both cutaneous (CL) and visceral leishmaniasis (VL). This study aimed to analyse trends in the clinical presentation, diagnosis, management, and epidemiology of leishmaniasis at Severo Ochoa University Hospital in Leganés, an endemic area in Southern Madrid affected by Europe’s largest outbreak (2009–2015). A retrospective study was conducted, including all confirmed cases from January 1992 to December 2024, using clinical records. Cases were stratified into pre-outbreak, outbreak, and post-outbreak periods. A total of 151 cases were identified, including 129 VL, 21 CL, and 1 simultaneous VL/CL. VL predominated among adults during the HIV epidemic, later shifting to elderly and non-HIV immunosuppressed patients, while paediatric cases remained stable. Diagnostic methods evolved from bone marrow microscopy, culture, and IFAT to molecular and chemiluminescence assays. VL treatment also evolved, with amphotericin B gradually replacing meglumine antimoniate as first-line VL treatment. Most patients required hospitalisation, with 8.5% mortality, mainly among immunocompromised or elderly individuals. A persistent concentration of cases near recently urbanised areas adjacent to the parks of Polvoranca and Bosquesur was observed. Despite advances in diagnosis and therapy, endemic transmission and underreporting continue, highlighting the need for ongoing surveillance and preventive measures. Hospital record review proved useful for monitoring compliance with mandatory VL notification, though its applicability to cutaneous cases remains limited.

## Linked entities

- **Chemicals:** amphotericin B (PubChem CID 1972), meglumine antimoniate (PubChem CID 64953)
- **Diseases:** leishmaniasis (MONDO:0011989), cutaneous leishmaniasis (MONDO:0005446), visceral leishmaniasis (MONDO:0005445)
- **Species:** Leishmania infantum (taxon 5671)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** pancytopenia (MESH:D010198), diabetes (MESH:D003920), ear, thorax and arm lesions (MESH:D004427), Leishmaniasis (MESH:D007896), injury to (MESH:D014947), diseases (MESH:D004194), MCL (MESH:D007897), headache (MESH:D006261), Pneumocystis jirovecii (MESH:D011020), lymphadenitis (MESH:D008199), CL) and visceral leishmaniasis (MESH:D007898), fever (MESH:D005334), neglected tropical diseases (MESH:D058069), cutaneous ( (MESH:D018366), leukopenia (MESH:D007970), cutaneous lesions (MESH:D009059), splenomegaly (MESH:D013163), urinary tract infection (MESH:D014552), genital candidiasis (MESH:D002181), infected (MESH:D007239), post (MESH:D000094025), thrombopenia (MESH:D013921), haematological disorders (MESH:D006402), hepatomegaly (MESH:D006529), CL (MESH:D002971), HIV-coinfected (MESH:D060085), CL (MESH:D016773), infectious (MESH:D003141), Brain toxoplasmosis (MESH:D014123), HIV (MESH:D015658), pulmonar aspergillosis (MESH:D001228), asthenia (MESH:D001247), oncologic (MESH:D000072716), anaemia (MESH:D000743), Oral candidiasis (MESH:D002180)
- **Chemicals:** meglumine antimoniate (MESH:D000077485), Bilirubin (MESH:D001663), amoxicillin/clavulanate (MESH:D019980), methotrexate (MESH:D008727), Amphotericin B (MESH:D000666), miltefosine (MESH:C039128), antimonials (-)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Phlebotomus (subgenus) [taxon 44556], Hepatitis C virus [taxon 11103], Leishmania infantum (species) [taxon 5671], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335], Human immunodeficiency virus 1 (no rank) [taxon 11676], Hepatitis B virus (no rank) [taxon 10407], Streptococcus pneumoniae (species) [taxon 1313], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Campylobacter jejuni (species) [taxon 197], Haemophilus influenzae (species) [taxon 727], Giardia duodenalis (species) [taxon 5741], Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Mycobacterium tuberculosis (species) [taxon 1773], Stenotrophomonas maltophilia (species) [taxon 40324], Hepatovirus A (no rank) [taxon 12092], Cytomegalovirus (genus) [taxon 10358], Leishmania donovani (species) [taxon 5661], Treponema pallidum (species) [taxon 160], Rotavirus (genus) [taxon 10912], Coxiella burnetii (species) [taxon 777], Neisseria gonorrhoeae (species) [taxon 485], Lepus (hares, genus) [taxon 9980], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943515/full.md

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Source: https://tomesphere.com/paper/PMC12943515