Evidence map›Paper›PMID 39105861›Full record

ArticleInternational journal of colorectal disease2024

Co-occurrence of oral pemphigus vulgaris and herpes simplex virus infection in a young patient with Crohn's disease: report of a rare case of oral lesions during anti-TFN alpha and immunomodulator therapy.

Danielle Nobre Lopes, Noêmia Pereira de Oliveira, Karla Cristina de Campos Augusto, Adrianna Milagres, Ana Luiza Miguez, Arley Silva Junior, Danielle Castex Conde, Karin Soares Cunha, Márcia Henriques Magalhães, Rafaela Elvira Rozza-de-Menezes

Abstract readCase Reports
In one paragraph

Article in International journal of colorectal disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

10 authors.

Danielle Nobre LopesPostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Noêmia Pereira de OliveiraPostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Karla Cristina de Campos AugustoSchool of Dentistry, Undergraduate Program, Universidade Federal Fluminense, Campus of Valonguinho, Niterói, RJ, Brazil.
Adrianna MilagresDepartment of Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Ana Luiza MiguezDepartment of Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Arley Silva JuniorPostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Danielle Castex CondePostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Karin Soares CunhaPostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil.
Márcia Henriques MagalhãesDepartment of Clinical Medicine, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Rafaela Elvira Rozza-de-MenezesPostgraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Empresa Brasileira de Serviços Hospitalares, Universidade Federal Fluminense, Av. Marquês Do Paraná, 303, 4O Andar, Sala 18Zip Code, Centro, Niterói, RJ, 24033-900, Brazil. rafaelarozza@id.uff.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPemphigus vulgaris (PV) is a potentially life-threatening mucocutaneous autoimmune disease that affects desmoglein-1 and desmoglein-3, leading to intraepithelial vesiculobullous lesions. In the oral mucosa, PV lesions can mimic other diseases such as mucous membrane pemphigoid, other forms of pemphigus, recurrent aphthous stomatitis, erythema multiforme, Stevens-Johnson syndrome, and virus-induced ulcers like herpes simplex virus (HSV), making diagnosis challenging. The co-occurrence of PV with Crohn's disease is rare and predominantly seen in younger patients. The therapeutic mainstay for both PV and Crohn's disease usually involves systemic corticosteroids combined with immunosuppressants and immunobiological drugs. Literature indicates that the use of these drugs, particularly TNF-alpha inhibitors, for managing autoimmune diseases like Crohn's can potentially induce other autoimmune diseases known as autoimmune-like syndromes, which include episodes of lupus-like syndrome and inflammatory neuropathies. There are few cases in the literature reporting the development of PV in individuals with CD undergoing infliximab therapy. CASE REPORT: A young female with severe Crohn's disease, treated with the TNF-alpha inhibitor infliximab, developed friable pseudomembranous oral ulcerations. Histopathological and immunofluorescence analyses confirmed these as PV. The treatment included clobetasol propionate and low-level photobiomodulation, which resulted in partial improvement. The patient later experienced severe intestinal bleeding, requiring intravenous hydrocortisone therapy, which improved both her systemic condition and oral lesions. Weeks later, new ulcerations caused by herpes virus and candidiasis were identified, leading to treatment with oral acyclovir, a 21-day regimen of oral nystatin rinse, and photodynamic therapy, ultimately healing the oral infections. To manage her condition, the gastroenterologists included methotrexate (25 mg) in her regimen to reduce the immunogenicity of infliximab and minimize corticosteroid use, as the patient was in remission for Crohn's disease, and the oral PV lesions were under control.

conclusionYoung patients with Crohn's disease should be referred to an oral medicine specialist for comorbidity investigation, as oral PV and opportunistic infections can arise during immunosuppressive therapy. The use of TNF-alpha inhibitors in patients treated for inflammatory bowel disease, such as Crohn's, should be carefully evaluated for potential side effects, including oral PV.

Indexed as

Crohn DiseaseHerpes SimplexImmunologic FactorsInfliximabPemphigusAdultFemaleHumansMouth DiseasesTumor Necrosis Factor-alphaImmunologic FactorsInfliximabTumor Necrosis Factor-alphaCrohn’s diseaseHerpes simplex virusImmunosuppressive therapyPemphigus vulgarisYoung patient

Identifiers

PMID39105861
PMCPMC11303579

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LicenceCC BY-NC-ND
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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.