Evidence map›Paper›PMID 39052026›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2024

Histoplasmosis in a fingolimod-treated patient: case report and scoping review.

Vítor Falcão de Oliveira, Guilherme Diogo da Silva, Larissa Teixeira Silva, Victor Lucas Gonçalves, Paula Emilia Rivas, Alexandre Coelho Marques, Mariane Taborda, Adriana Satie Gonçalves Kono Magri, Samira Luisa Apóstolos-Pereira, Dagoberto Callegaro and 1 more

Abstract readCase ReportsScoping Review
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Vítor Falcão de OliveiraUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Departamento de Moléstias Infecciosas e Parasitárias, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-2097-389X
Guilherme Diogo da SilvaUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Neurologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-9764-3763
Larissa Teixeira SilvaUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Neurologia, São Paulo, São Paulo, Brazil.
Victor Lucas GonçalvesUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Patologia, São Paulo, São Paulo, Brazil.
Paula Emilia RivasUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Patologia, São Paulo, São Paulo, Brazil.
Alexandre Coelho MarquesUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Neurologia, São Paulo, São Paulo, Brazil.
Mariane TabordaUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Departamento de Moléstias Infecciosas e Parasitárias, São Paulo, São Paulo, Brazil.
Adriana Satie Gonçalves Kono MagriUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Departamento de Moléstias Infecciosas e Parasitárias, São Paulo, São Paulo, Brazil.
Samira Luisa Apóstolos-PereiraUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Neurologia, São Paulo, São Paulo, Brazil.
Dagoberto CallegaroUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas Departamento de Neurologia, São Paulo, São Paulo, Brazil.
Marcello Mihailenko Chaves MagriUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Departamento de Moléstias Infecciosas e Parasitárias, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-7996-8265

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fingolimod is a sphingosine-1-phosphate receptor modulator used to treat multiple sclerosis. While fingolimod has been associated with an increased risk of cryptococcal meningitis, its correlation with other deep mycoses remains unclear. In this study, we conducted a scoping review of fingolimod associated with histoplasmosis, based on a case report, a literature review, and data from the FDA Adverse Events Reporting System (FAERS) as of January 24th, 2023. A 30-year-old Brazilian woman diagnosed with relapsing-remitting multiple sclerosis, receiving a daily dose of 0.5 mg of fingolimod, presented with a two-month history of fever and unintended weight loss, accompanied by lymphadenopathy, splenomegaly, and lung involvement was investigated. Biopsy of a lung nodule revealed fungal structures suggestive of Histoplasma sp. Additionally, serological testing yielded positive for Histoplasma capsulatum. Disseminated histoplasmosis should be considered in the differential diagnosis of febrile syndromes in patients undergoing fingolimod therapy for multiple sclerosis, particularly in the Americas, where this mycosis is endemic. Treatment with itraconazole and modification of immunotherapy can achieve excellent clinical outcomes.

Indexed as

Fingolimod HydrochlorideHistoplasmosisMultiple Sclerosis, Relapsing-RemittingAdultAntifungal AgentsFemaleHistoplasmaHumansImmunosuppressive AgentsAntifungal AgentsFingolimod HydrochlorideImmunosuppressive Agents

Identifiers

PMID39052026
PMCPMC11251513

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Registered trials

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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.