Evidence map›Paper›PMID 40084558›Full record

ArticleJournal of investigative medicine high impact case reports

Autoimmune Pulmonary Alveolar Proteinosis: A Rare Diagnosis in Pediatric Age.

Inês Pais-Cunha, Augusta Gonçalves, Sara Paulino, José Fontoura Matias, Silva Sónia, Catarina Ferraz, Inês Azevedo

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of investigative medicine high impact case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Inês Pais-CunhaServiço de Pediatria, UAG da Mulher e da Criança, ULS São João, Porto, PortugalULS São João, Porto, Portugal.ORCID 0000-0001-5368-0335
Augusta GonçalvesServiço de Pediatria, ULS Braga, Braga, Portugal.
Sara PaulinoServiço de Pediatria, UAG da Mulher e da Criança, ULS São João, Porto, PortugalULS São João, Porto, Portugal.
José Fontoura MatiasFaculdade de Medicina da Universidade do Porto, Porto, Portugal.
Silva SóniaFaculdade de Medicina da Universidade do Porto, Porto, Portugal.
Catarina FerrazFaculdade de Medicina da Universidade do Porto, Porto, Portugal.
Inês AzevedoFaculdade de Medicina da Universidade do Porto, Porto, Portugal.ORCID 0000-0002-0090-8612

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune pulmonary alveolar proteinosis (AI-PAP) is a rare condition, especially in children. The clinical presentation ranges from asymptomatic forms to respiratory distress requiring ventilation. We describe the case of a 13-year-old adolescent male who presented to the emergency department with acute pleuritic chest pain not associated with systemic complaints. On examination, he had diminished breath sounds in the lower two thirds of the chest with no other abnormal findings; SpO

Indexed as

Autoimmune DiseasesPulmonary Alveolar ProteinosisAdolescentHumansLungMaleTomography, X-Ray Computedautoimmunitypulmonary alveolar proteinosisradiography

Identifiers

PMID40084558
PMCPMC11909686

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.