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Erysipelas

Infectious Diseases · NLM MeSH · updated 2026-10-29 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

An acute infection of the skin caused by species of streptococcus.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (891 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

An acute infection of the skin caused by species of streptococcus. This disease most frequently affects infants, young children, and the elderly. Characteristics include pink-to-red lesions that spread rapidly and are warm to the touch. The commonest site of involvement is the face.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Where it fits in the MeSH classification

Broader topics
Streptococcal Infections; Skin Diseases, Bacterial

Related concepts

  • Streptococcus

Research landscape

PubMed indexes 1,431 records tagged with the MeSH heading “Erysipelas” (counts retrieved 2026-10-29). 93 of them (6.5%) were published from 2020 onward, and the busiest period so far is through 1999 with 899 records.

Reviews account for 145 records (10.1%) and meta-analyses for 6. Randomized controlled trials number 12 (0.8%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 899 records; 2000-2009: 224 records; 2010-2019: 215 records; 2020 onward: 93 records899through 19992242000-20092152010-2019932020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 1999899
2000-2009224
2010-2019215
2020 onward93
Share of records by publication typeReviews: 10.1 percent; Meta-analyses: 0.4 percent; Randomized controlled trials: 0.8 percentReviews10.1% (145)Meta-analyses0.4% (6)Randomized controlled trials0.8% (12)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 1,431 PubMed records
TypeRecordsShare
Reviews14510.1%
Meta-analyses60.4%
Randomized controlled trials120.8%

Method: PubMed query "Erysipelas"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-29.

Reading the evidence in infectious diseases

Infectious disease evidence combines microbiology, epidemiology and clinical trials. Laboratory studies identify pathogens and how they cause harm; surveillance and outbreak investigations describe who is affected and how infection spreads; trials establish whether treatments and vaccines work. Results depend on place and time, because pathogens evolve and resistance patterns and population immunity change. Check when and where the data were collected, how cases were defined and how up to date the evidence is.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Erysipelas, a large retrospective study of aetiology and clinical presentation
Bläckberg A, Trell K, Rasmussen M
2015Research article
Design not recorded in structured metadata
46cc by
PMID 26424182 · DOI · PMC4590694
The efficacy and safety of daptomycin vs. vancomycin for the treatment of cellulitis and erysipelas
Pertel PE, Eisenstein BI, Link AS, Donfrid B, Biermann EJ, Bernardo P, et al.
2009Randomized controlled trial
Design not recorded in structured metadata
41cc by
PMID 19222623 · DOI · PMC2705813
Recurrent erysipelas--risk factors and clinical presentation
Inghammar M, Rasmussen M, Linder A
2014Research article
Design not recorded in structured metadata
35cc by
PMID 24884840 · DOI · PMC4033615
Immune parameters monitored during the production period of laying hens managed with or without single-dose vaccination against erysipelas
Wattrang E, Näslund K, Tamminen LM, Söderlund R, Sørensen Dalgaard T, Jansson DS, et al.
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42063043 · DOI · PMC13137716

Erysipelas, a large retrospective study of aetiology and clinical presentation [1]

Research article Bläckberg A, Trell K, Rasmussen M · · 2015 · cited 46 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundErysipelas is a common and severe infection where the aetiology and optimal management is not well-studied.
Closing excerpt
aureus in erysipelas remains elusive.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (191 words)

BackgroundErysipelas is a common and severe infection where the aetiology and optimal management is not well-studied. Here, we investigate the clinical features, bacteriological aetiology, and treatment of erysipelas.MethodsEpisodes of erysipelas in a seven-years period in our institution were studied retrospectively using a pre-specified protocol and is presented with descriptive and comparative statistics.Results1142 episodes of erysipelas were identified in 981 patients. Patients had a median age of 61 years, 59 % were male, a majority had underlying diseases or predisposing conditions, and the leg was most often affected. Wound cultures were taken in 343 episodes and 56 grew group A streptococci (GAS), 53 grew group G streptococci (GGS), 11 grew group C streptococci (GCS), and 153 grew Staphylococcus aureus. Blood cultures were drawn in 49 % of episodes and 50 cultures were positive with GGS as the most common finding (21 cultures) followed by GAS in 13, group B streptococci in 5, S. aureus in 4, and GCS in 3 cultures. In 45 % of episodes, patients received antibiotics with activity against S. aureus.ConclusionsGGS is the most common streptococcus isolated in erysipelas and the role of S. aureus in erysipelas remains elusive.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 26424182 · DOI · PMC4590694

The efficacy and safety of daptomycin vs. vancomycin for the treatment of cellulitis and erysipelas [2]

Randomized controlled trial Pertel PE, Eisenstein BI, Link AS, Donfrid B, Biermann EJ, Bernardo P, et al. · · 2009 · cited 41 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundResults from previous trials suggest that daptomycin may result in faster clinical improvement than penicillinase-resistant penicillins or vancomycin for patients with complicated skin and skin structure infections.
Closing excerpt
Daptomycin 4 mg/kg once daily appeared to be effective and safe for treating cellulitis or erysipelas.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (172 words)

BackgroundResults from previous trials suggest that daptomycin may result in faster clinical improvement than penicillinase-resistant penicillins or vancomycin for patients with complicated skin and skin structure infections.ObjectiveThe objective was to evaluate whether daptomycin treatment of cellulitis or erysipelas would result in faster resolution compared with vancomycin.DesignThe study was a prospective, evaluator-blinded, multi-centre trial. Patients were randomised to receive daptomycin 4 mg/kg once daily or vancomycin according to standard of care for 7-14 days.PatientsAdults diagnosed with cellulitis or erysipelas requiring hospitalisation and intravenous antibiotic therapy were eligible for enrolment.ResultsThe clinical success rates were 94.0% for daptomycin and 90.2% for vancomycin (95% confidence interval for the difference, -6.7%, 14.3%). There were no statistically significant differences between treatment arms in the time to resolution or improvement in any of the predefined clinical end-points. Both daptomycin and vancomycin were well tolerated.ConclusionsThere was no difference in the rate of resolution of cellulitis or erysipelas among patients treated with daptomycin or vancomycin. Daptomycin 4 mg/kg once daily appeared to be effective and safe for treating cellulitis or erysipelas.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 19222623 · DOI · PMC2705813

Recurrent erysipelas--risk factors and clinical presentation [3]

Research article Inghammar M, Rasmussen M, Linder A · · 2014 · cited 35 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundErysipelas is a common infection that often recurs, but the impact of specific risk factors for reoccurrence remains elusive.
Closing excerpt
ConclusionsIn this large cross-sectional study of over 500 patients with erysipelas, lymphedema was the most prominent risk factors for recurrence although the distribution of predisposing conditions varies depending on the site of erysipelas.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (236 words)

BackgroundErysipelas is a common infection that often recurs, but the impact of specific risk factors for reoccurrence remains elusive. In the present study we aimed at clarifying predisposing conditions for reoccurrence.MethodsMedical records were reviewed from all patients ≥18 years of age diagnosed with erysipelas at the Department of Infectious Diseases at Skåne University Hospital, Sweden, from January 2007 to February 2011. 502 patients were included, of which 357 were single episode erysipelas and 145 had recurrent erysipelas. These two groups were compared regarding underlying conditions and clinical presentation.ResultsErysipelas in the lower limbs had the greatest propensity of recurrence. The associations between underlying conditions and recurrence were largely depending on the site of erysipelas. Overall, the most prominent risk factor for recurrence was lymphedema and other conditions causing a chronic impairment of the defence against microbes. Conditions temporarily disrupting the skin barrier (e.g. a local wound or toe web intertrigo), although likely being risk factors for erysipelas per se, did not seem to predispose to repeated episodes. Individuals with recurrent erysipelas tended to seek medical attention earlier, and were less likely to be hospitalized or receive intravenous antibiotics, but there was no evidence of any difference in inflammatory reaction when taking confounding factors into account.ConclusionsIn this large cross-sectional study of over 500 patients with erysipelas, lymphedema was the most prominent risk factors for recurrence although the distribution of predisposing conditions varies depending on the site of erysipelas.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 24884840 · DOI · PMC4033615

Immune parameters monitored during the production period of laying hens managed with or without single-dose vaccination against erysipelas [4]

Research article Wattrang E, Näslund K, Tamminen LM, Söderlund R, Sørensen Dalgaard T, Jansson DS, et al. · · 2026

Abstract reading summary — source excerpts
Opening excerpt
BackgroundErysipelas, caused by infection with Erysipelothrix rhusiopathiae (ER), is an emerging disease in non-cage housed laying hens.
Closing excerpt
Nonetheless, among the parameters studied we found no evidence to suggest that antibody responses to single-dose vaccination should fail or why older flocks seem more susceptible to erysipelas outbreaks.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (292 words)

BackgroundErysipelas, caused by infection with Erysipelothrix rhusiopathiae (ER), is an emerging disease in non-cage housed laying hens. According to Swedish field experience outbreaks seem more common in older flocks and may also occur in flocks vaccinated against erysipelas. This cross-sectional study aimed to assess single-dose vaccination outcome in laying hens with respect to antibody titres to ER and to monitor selected immune parameters to identify putative risk factors for erysipelas. Blood samples were collected from laying hen flocks at 30, 50 and 75 weeks of age. At each time point, 5 unvaccinated flocks and 5 flocks that had been vaccinated against erysipelas once at placement were sampled (20 hens/flock, total n=600).ResultsThe results showed that the majority of hens were positive for IgY to ER and that the antibody titres were higher in older hens irrespective of vaccination status. Vaccinated hens had significantly higher IgY titres to ER compared to those of unvaccinated hens. This difference was most prominent for the youngest age category. Among the different leukocyte populations studied, blood heterophil, monocyte and γ/δTCR+ T-cell counts were significantly higher in younger hens. Also, serum MBL-levels were significantly higher in younger hens and MBL-levels were positively correlated to heterophil and monocyte counts at the individual level.ConclusionsTaken together, results indicate that ER or antigenically similar bacteria are common in the hen environment and that this exposure results in antibodies recognising ER that are present at higher levels in older laying hens. In addition, a higher general pathogen load/level of subclinical infections was indicated by altered leukogram patterns and increased MBL-levels in the youngest age category. Nonetheless, among the parameters studied we found no evidence to suggest that antibody responses to single-dose vaccination should fail or why older flocks seem more susceptible to erysipelas outbreaks.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42063043 · DOI · PMC13137716

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Coley's toxins, tumor necrosis factor and cancer research: a historical perspective [5]
    Wiemann B, Starnes CO · Pharmacol Ther · 1994 · cited 306 times (Europe PMC)
  • Research article A systematic review of bacteremias in cellulitis and erysipelas [6]
    Gunderson CG, Martinello RA · J Infect · 2012 · cited 88 times (Europe PMC)
  • Research article Erysipelas: recognition and management [7]
    Bonnetblanc JM, Bédane C · Am J Clin Dermatol · 2003 · cited 69 times (Europe PMC)
  • Research article Erysipelas [8]
    Chartier C, Grosshans E · Int J Dermatol · 1990 · cited 53 times (Europe PMC)
  • Research article Interventions for cellulitis and erysipelas [9]
    Kilburn SA, Featherstone P, Higgins B, Brindle R · Cochrane Database Syst Rev · 2010 · cited 48 times (Europe PMC)
  • Research article Interventions for the prevention of recurrent erysipelas and cellulitis [10]
    Dalal A, Eskin-Schwartz M, Mimouni D, Ray S, Days W, Hodak E, et al. · Cochrane Database Syst Rev · 2017 · cited 42 times (Europe PMC)

References

  1. Bläckberg A, Trell K, Rasmussen M. Erysipelas, a large retrospective study of aetiology and clinical presentation. . 2015. PMID 26424182 · DOI · PMC4590694
  2. Pertel PE, Eisenstein BI, Link AS, Donfrid B, Biermann EJ, Bernardo P, et al.. The efficacy and safety of daptomycin vs. vancomycin for the treatment of cellulitis and erysipelas. . 2009. PMID 19222623 · DOI · PMC2705813
  3. Inghammar M, Rasmussen M, Linder A. Recurrent erysipelas--risk factors and clinical presentation. . 2014. PMID 24884840 · DOI · PMC4033615
  4. Wattrang E, Näslund K, Tamminen LM, Söderlund R, Sørensen Dalgaard T, Jansson DS, et al.. Immune parameters monitored during the production period of laying hens managed with or without single-dose vaccination against erysipelas. . 2026. PMID 42063043 · DOI · PMC13137716
  5. Wiemann B, Starnes CO. Coley's toxins, tumor necrosis factor and cancer research: a historical perspective. Pharmacol Ther. 1994. PMID 7724661 · DOI
  6. Gunderson CG, Martinello RA. A systematic review of bacteremias in cellulitis and erysipelas. J Infect. 2012. PMID 22101078 · DOI
  7. Bonnetblanc JM, Bédane C. Erysipelas: recognition and management. Am J Clin Dermatol. 2003. PMID 12627991 · DOI
  8. Chartier C, Grosshans E. Erysipelas. Int J Dermatol. 1990. PMID 2228369 · DOI
  9. Kilburn SA, Featherstone P, Higgins B, Brindle R. Interventions for cellulitis and erysipelas. Cochrane Database Syst Rev. 2010. PMID 20556757 · DOI · PMC8693180
  10. Dalal A, Eskin-Schwartz M, Mimouni D, Ray S, Days W, Hodak E, et al.. Interventions for the prevention of recurrent erysipelas and cellulitis. Cochrane Database Syst Rev. 2017. PMID 28631307 · DOI · PMC6481501

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-29.

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At a glance

1,431
PubMed records on this heading
6%
published since 2020
145
review articles
12
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-29; they show how much has been written, not how strong the evidence is.

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