2.2.3 Erysipelas

Grading & Level of Importance: A

ICD-11

1B70

Synonyms

Cellulitis (in Anglosphere).

Epidemiology

Prevalence around 1100 /100.000 per year. 

Read more

Prevalence around 1100 /100,000 per year. Peak incidence around 60 to 80 years.

Definition

An acute cutaneous bacterial infection that involves first the superficial lymphatics with fast spreading in the upper dermis and, if not properly treated, may penetrate depending on the virulence of the microbe and the susceptibility of the host into deeper layers including the adipose tissue and fascia and muscle (necrotizing fasciitis).

Aetiology & Pathogenesis

The site of entry often is in between toes, in skin folds or in superficial erosions. Causative agents are about 90% beta-hemolytic group A streptococci (less B,C,G) or Staphylococcus aureus and sometimes gram-positive or - negative bacteria. 90% are localized at the lower extremity, 2.5% in the face.

Read more

Erysipelas affects all ethnic groups without a gender specifity. The site of entry is often between toes, in skin folds or from superficial erosions. Trauma, infected arthropod reactions, lymphedema, varicose vein surgery and other surgical procedures at the leg site (bypass donor site), arteriosclerotic and diabetic ulcers on the lower leg also predispose.

Comorbidities such as hypertension, diabetes type 2 (DM2), chronic lymphedema and obesity being the most common.

Causative agents are about 90% beta-hemolytic group A streptococci (less B, C, G) or Staphylococcus aureus and sometimes gram-positive or - negative bacteria. However, the role of Staphylococcus aureus, and specifically methicillin-resistant S aureus (MRSA), remains controversial. Some evidence exist that co-colonizing S.aureus exfoliative toxins contribute to the bullous subtype. 90% of cases are localized on the lower extremity, 2.5% on the face.

Signs & Symptoms

Acute illness with fever, chills (often missing in recurrent disease and in the elderly), sharply bordered, warm, tender, oedematous, erythematous plaques with flame-like peripheral spread. Bullous, haemorrhagic or necrotic presentations are more severe variants.

Read more

Erysipelas is an acute illness with high fever and chills (often missing in recurrent disease and in the elderly), sharply bordered, warm, tender, oedematous, erythematous plaques with flame-like peripheral spread.

Bullous, haemorrhagic or necrotic presentations are more severe variants. In immune-compromised patients, erysipelas saltans with very fast spreading may occur. The necrotic gangrenescens subtype is accompanied by danger of deeper localization with necrotizing fasciitis – an early surgical intervention is necessary to stop the severe course.

Localisation

Erysipelas can affect any site, although it has a predilection for the face and legs. Chronic edema of the leg is predisposing. In the face often spreading to the opposite site.

Classification

Uncomplicated type, vesicular- bullous or hemorrhagic type, necrotic /gangrenous type. 

Read more

There are different courses of the disease but no classification. However, subtypes are:

  • uncomplicated type

  • vesicular

  • bullous or

  • hemorrhagic type

  • saltans type and

  • necrotic /gangrenescens type

Laboratory & other workups

Erythrocyte sedimentation rate (ESR) and C reactive protein (CRP) elevated, later ASL/AST titres rises with a leukocytosis.

Dermatopathology

Dermal edema with dilation of upper and deep vessel plexus. Masses of polymorphous neutrophils between collagen bundles, later with necrotic areas. 

Course

Either short, high fever and fast response to anti-streptococcal antibiotics or complicated when deeper penetrating and host defence is low. 

Complications

Lymphoedema (especially with recurrent disease), myocarditis, pneumonia, glomerulonephritis. Sepsis < 5%. Thrombosis (if occurring on the face this can result in venous sinus thrombosis). Abscess formation.

Diagnosis

Clinical features (fever, erythema), culture of possible entry point (tinea pedis between the toes or nasal swab), inflammatory markers.

Differential Diagnosis

Acute contact dermatitis, thrombophlebitis, erysipeloid, acrodermatitis chronica atrophicans (inflammatory stage), large phlegmon of the lower leg, be careful not to miss necrotising fasciitis.

Read more
  • acute contact dermatitis and stasis dermatitis,

  • thrombophlebitis,

  • erysipeloid and cellulitis,

  • acrodermatitis chronica atrophicans (inflammatory stage),

  • acute compartment syndrome.

Danger: be careful not to miss early stage of necrotising fasciitis.

Prevention & Therapy

Bed rest, involved region elevated, cool moist compresses, systemic antibiotics (penicillin 4-5 million IU daily i.v. or 4 x 500 mg oral or amoxicillin in uncomplicated cases, alternatively amoxicillin/clavulanate; severe erysipelas need hospitalization and thrice or four times daily 5 to 10. Mill. Units penicillin, if resistant, cephalosporins) for around 7-10 days. Clindamycin is an alternative, especially if penicillin allergy present.

Read more

Avoiding scratching of skin lesions, wet interdigital and intertriginous areas. In chronic lymphedema and relapsing erysipelas high hygiene standards are necessary.

Therapy :

Bed rest, involved region elevated, cool moist compresses, systemic antibiotics (penicillin 4-5 million IU daily i.v. or 4 x 500 mg oral in uncomplicated cases, alternatively ampicillin/clavulanate.

Severe erysipelas need hospitalization and thrice or four times daily 5 to 10. Mill. units penicillin, if resistant, cephalosporins for 10 days. Clindamycin if penicillin allergy present.

Special

Necrotizing deep penetrating type with development into necrotizing fasciitis early intervention by surgery.


In severe lymphoedema with relapsing erysipelas maintenance treatment (on/off). Inpatients can be treated with concomitant intermittent lymph-compression during antibiotic infusion.

Comments

Be the first one to leave a comment