ArticlePostepy dermatologii i alergologii2025
A rare allergic disease due to mosquito bite: Skeeter syndrome.
Article in Postepy dermatologii i alergologii, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Case Report: Localized hyperinflammatory response in the bulla after mosquito bites in a patient with systemic lupus erythematosus.Frontiers in immunology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Severe allergic reactions to mosquito bites are rarely seen. Aim: To determine the demographic and distinguishing clinical characteristics of Skeeter syndrome, a severe allergic reaction to mosquito allergy, in childhood. Material and methods: All patients diagnosed with Skeeter syndrome who presented to our Pediatric Allergy and Immunology outpatient clinic between January 2019 and December 2024 were included in the study. The demographic, laboratory, and clinical data of the patients were retrospectively obtained from the hospital's computerized database. Results: A total of 15 patients with a mean age of 4.4 ±3.2 years were included in the study, of whom 11 (73%) were male. Eight (50%) patients had an additional atopic disease, 13 (86.6%) had recurrent Skeeter syndrome, 8 (50%) had a family history of atopy in first-degree relatives, and 2 (13%) had a family history of a similar disease in first-degree relatives. In 11 (73%) patients, induration was accompanied by a bullous lesion. In 4 (27%) patients, induration resembling cellulitis was present without bullous formation. The induration diameters ranged from 5 to 20 cm, while bullous lesions ranged from 1 to 5 cm. Pruritus was present in 12 (80%) patients, tenderness in 3 (20%), and low-grade fever in 1 patient. The treatment duration ranged from 7 to 14 days. None of the patients had an identified immunodeficiency. Conclusions: Skeeter syndrome is a recurrent allergic disease. The presence of vesicles/bullae at the center of a large local reaction, along with a detailed medical history, is a distinguishing feature.
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.