Evidence map›Paper›PMID 38055375›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2023

Can COVID-19 impact the natural history of paracoccidioidomycosis? Insights from an atypical chronic form of the mycosis.

César Augusto Tomaz de Souza, Cesar Cilento Ponce, Gisele Burlamaqui Klautau, Nathan Costa Marques, Wladimir Queiroz, Rosely Antunes Patzina, Gil Benard, José Angelo Lauletta Lindoso

Erratum issuedOpen access · diamondAbstract readCase Reports
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 39% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

César Augusto Tomaz de SouzaInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-1413-4918
Cesar Cilento PonceInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.
Gisele Burlamaqui KlautauInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.
Nathan Costa MarquesUniversidade de São Paulo, Faculdade de Medicina, Departamento de Cardio-Pneumologia, São Paulo, São Paulo, Brazil.
Wladimir QueirozInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.
Rosely Antunes PatzinaInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.
Gil BenardUniversidade de São Paulo, Faculdade de Medicina, Instituto de Medicina Tropical de São Paulo, Laboratório de Micologia Médica (LIM-53), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-5469-3602
José Angelo Lauletta LindosoInstituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-4405-4401
Instituto de Infectologia Emílio Ribas · BRUniversidade de São Paulo · BRInstituto Adolfo Lutz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paracoccidioidomycosis (PCM) is a systemic fungal infection caused by Paracoccidioides spp. It can occur as an acute/subacute form (A/SAF), a chronic form (CF) and rarely as a mixed form combining the features of the two aforementioned forms in an immunocompromised patient. Here, we report a 56-year-old male patient with CF-PCM who presented with atypical manifestations, including the development of an initial esophageal ulcer, followed by central nervous system (CNS) lesions and cervical and abdominal lymphatic involvement concomitant with severe SARS-CoV-2 infection. He was HIV-negative and had no other signs of previous immunodeficiency. Biopsy of the ulcer confirmed its mycotic etiology. He was hospitalized for treatment of COVID-19 and required supplemental oxygen in the intensive unit. The patient recovered without the need for invasive ventilatory support. Investigation of the extent of disease during hospitalization revealed severe lymphatic involvement typical of A/SAF, although the patient`s long history of high-risk exposure to PCM, and lung involvement typical of the CF. Esophageal involvement is rare in non-immunosuppressed PCM patients. CNS involvement is also rare. We suggest that the immunological imbalance caused by the severe COVID-19 infection may have contributed to the patient developing atypical severe CF, which resembles the PCM mixed form of immunosuppressed patients. Severe COVID-19 infection is known to impair the cell-mediated immune response, including the antiviral response, through T-lymphopenia, decreased NK cell counts and T-cell exhaustion. We hypothesize that these alterations would also impair antifungal defenses. Our case highlights the potential influence of COVID-19 on the course of PCM. Fortunately, the patient was timely treated for both diseases, evolving favorably.

Indexed as

COVID-19ParacoccidioidesParacoccidioidomycosisAntifungal AgentsHumansMaleMiddle AgedSARS-CoV-2UlcerAntifungal Agents

Identifiers

PMID38055375
PMCPMC10691805
OpenAlexW4389222928

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.