Erythema Nodosum

BASICS

BASICS

BASICS

DESCRIPTION

DESCRIPTION

DESCRIPTION

  • A delayed-type IV hypersensitivity reaction to various antigens, or an autoimmune reaction presenting as a panniculitis (1) that affects subcutaneous fat
  • The clinical pattern of multiple, bilateral, erythematous, tender nodules in a typically anterior pretibial distribution that undergo a characteristic pattern of color changes, similar to that seen in bruises. Unlike erythema induratum, the lesions of erythema nodosum (EN) do not typically ulcerate.
  • Occurs most commonly on the shins; less commonly on the thighs, forearms, trunk, head, or neck
  • Often associated with nonspecific prodrome including fever, weight loss, and arthralgia
  • Often idiopathic but may be associated with a number of clinical entities
  • Usually remits spontaneously in weeks to months without scarring, atrophy, or ulceration
  • Uncommon to have recurrences after the initial presentation
  • Divided into acute (more common) and chronic (rare)

Pregnancy Considerations
May have repeat outbreaks during pregnancyPediatric Considerations
A rare pediatric variant has lesions only on palms or soles, often unilateral; typically has a shorter duration in children than in adults

EPIDEMIOLOGY

EPIDEMIOLOGY

EPIDEMIOLOGY

Frequently observed in women aged 18 to 34 years

Incidence

Incidence

Incidence

  • 1 to 5/100,000/year
  • Predominant age: 20 to 30 years
  • Predominant sex: female > male (6:1) in adults

Prevalence

Prevalence

Prevalence

  • Varies geographically depending on the prevalence of disorders associated with EN
  • Reported 1 to 5/100,000

ETIOLOGY AND PATHOPHYSIOLOGY

ETIOLOGY AND PATHOPHYSIOLOGY

ETIOLOGY AND PATHOPHYSIOLOGY

  • Idiopathic: up to 55%
  • Infectious: 44%; streptococcal pharyngitis (most common), mycobacteria, mycoplasma, chlamydia, mycoplasma, coccidioidomycosis, rarely can be caused by Campylobacter spp., Rickettsiae, Salmonella spp., psittacosis, syphilis
  • Sarcoidosis: 11–25%
  • Drugs: 3–10%; sulfonamides, amoxicillin, oral contraceptives, bromides, azathioprine, vemurafenib
  • Pregnancy: 2–5%
  • Enteropathies: 1–4%; ulcerative colitis, Crohn disease, Behçet disease, celiac disease, diverticulitis
  • Rare causes: <1% (2)
    • Fungal: dermatophytes, coccidioidomycosis, histoplasmosis, blastomycosis, Kerion of Celso
    • Viral/chlamydial: infectious mononucleosis; lymphogranuloma venereum; paravaccinia; HIV; hepatitis B, C
    • Malignancies: lymphoma/leukemia, sarcoma, myelodysplastic syndrome
    • Vasculitis: Takayasu arteritis
    • Sweet syndrome (acute febrile neutrophilic dermatosis)
    • Sorafenib, pembrolizumab, dupilumab
    • COVID-19 virus, SARS-CoV-2 vaccine (3)

Genetics

Genetics

Genetics

A positive family history is usually associated with infectious etiologies.

RISK FACTORS

RISK FACTORS

RISK FACTORS

See “Etiology and Pathophysiology.”

COMMONLY ASSOCIATED CONDITIONS

COMMONLY ASSOCIATED CONDITIONS

COMMONLY ASSOCIATED CONDITIONS

See “Etiology and Pathophysiology.”

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