Evidence map›Paper›PMID 39186781›Full record

ArticlePLoS neglected tropical diseases2024

VL-HIV co-infection with Leishmania containing skin lesions resembling para-kala-azar dermal leishmaniasis.

Natália O Alves, Jéssica A Oshiro, Yunna C Silva, Gabriela C Pacher, Aline E Casaril, Yasmin S Rizk, Silvia N O Uehara, Anamaria M M Paniago, Isadora L X Andrade, Carla C P Arruda and 1 more

Abstract readCase Reports
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Easy Identification ofACS omega · 2025
    Article
  6. An Update on Clinical and Pathogenic Spectra of Leishmaniasis.Expert reviews in molecular medicine · 2025
    Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Natália O AlvesLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Jéssica A OshiroFaculty of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Yunna C SilvaFaculty of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Gabriela C PacherLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Aline E CasarilLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Yasmin S RizkLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Silvia N O UeharaFaculty of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Anamaria M M PaniagoGraduate Program in Infectious and Parasitic Diseases, Faculty of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Isadora L X AndradeMaria Aparecida Pedrossian University Hospital-Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Carla C P ArrudaLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Alessandra G OliveiraLaboratory of Human Parasitology, Institute of Biosciences, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.ORCID 0000-0002-7677-9351

Funding

Fundação de Apoio ao Desenvolvimento do Ensino, Ciência, e Tecnologia do Estado de Mato Grosso do Sul- FUNDECT 99/2023 SIAFIC 33115
6 · The paper itself

Abstract

Leishmaniases are a group of neglected vector-borne infectious diseases that are among the six priority endemic diseases worldwide. Visceral leishmaniasis (VL) is the most severe clinical manifestation, characterized by systemic and chronic visceral involvement and high mortality in immunosuppressed and untreated patients. VL can be complicated into post-kala-azar dermal leishmaniasis (PKDL), and when dermatologic disorders occur simultaneously with active VL, an intermediate clinical form called para-kala-azar dermal leishmaniasis (para-KDL) occurs. This clinical form is of great epidemiological relevance, as humans act as a source of infection for vectorial transmission. In the Americas, Brazil is among the seven countries responsible for more than 90% of VL cases, though reports of PKDL and para-KDL are rare. This paper presents three cases of VL-HIV co-infection with Leishmania-containing skin lesions resembling para-kala-azar dermal leishmaniasis. The cases were investigated by the team from the Infectious Diseases Department of University Hospital (HUMAP/UFMS) in Mato Grosso do Sul, Brazil. The three patients exhibited skin lesions where amastigote forms of L. (L.) infantum were identified. All cases exhibited similar clinical manifestations of para-KDL, including fever, hepatosplenomegaly, pancytopenia, and disseminated skin lesions. The study described the prevalence of comorbidities, the incidence of VL relapse, and the therapeutic regimen in relation to the outcomes. The study underscores the importance of follow-up and secondary prophylaxis in patients with VL, which are essential for the efficacy of the treatment. Furthermore, the study provides insight into the potential epidemiological profile of para-KDL cases in Brazil, which contributes to the development of more efficient clinical management strategies for patients.

Indexed as

CoinfectionHIV InfectionsLeishmaniasis, CutaneousLeishmaniasis, VisceralAdultBrazilFemaleHumansLeishmania infantumMaleMiddle AgedSkin

Identifiers

PMID39186781
PMCPMC11379370

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.