ArticleInternational journal of clinical pediatric dentistry2026
Oral Manifestations of Sweet Syndrome in a Child: A Case Report.
Article in International journal of clinical pediatric dentistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sweet syndrome is a relatively rare disease characterized by neutrophilia, tender and erythematous skin lesions with sudden onset of fever. Oral involvement is usually rare. We report a case of a 5-year-old boy who presented with fever, spontaneous erythematous swelling over the right periorbital and suprasternal region, upper left lip swelling, generalized gingival hyperplasia over the upper gingiva, and a single ulcer on the right soft palate region. Blood results was consistent with bicytopenia and leukocytosis, while biopsy of the skin and gingival lesions revealed dense infiltration of mixed inflammatory cells composed predominantly of neutrophils. Sweet syndrome was suggested based on the clinical presentations and histological features. Steroid treatment was initiated according to the suggested protocol; unfortunately, the child's condition started to deteriorate 3 weeks after his initial presentation, and he passed away 2 weeks later due to massive intracranial bleeding. Proper investigation and screening are crucial when any oral lesions with unknown causes are encountered.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.