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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Erythema nodosum

Dermatology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Toxic, ulcerating or vascular mimic

Shock, severe pain out of proportion, crepitus, rapidly spreading unilateral inflammation, a cold swollen limb, purpura, ulceration or major respiratory compromise is not typical uncomplicated erythema nodosum and may represent deep infection, thrombosis, vasculitis or another panniculitis.

Action: Arrange same-day emergency assessment with sepsis treatment, vascular imaging or specialist tissue sampling directed by the threat; do not inject corticosteroid or reassure on the basis of tender nodules alone.

Synopsis

Recognise erythema nodosum as a tender septal panniculitis across skin tones, investigate likely infectious, inflammatory, medicine and pregnancy triggers proportionately, and identify atypical nodules needing biopsy or urgent reassessment.

  • Erythema nodosum causes crops of hot tender subcutaneous nodules, classically symmetrical over anterior shins, with poorly defined edges and no ulceration.
  • Lesions evolve like bruises over several weeks from red or violaceous to brown, green-yellow or hyperpigmented and heal without atrophic scar.
  • In brown or black skin, warmth, deep tenderness and swelling may identify active nodules more reliably than erythema; record residual pigment separately from pain and inflammation.
  • Fever, malaise and bilateral ankle pain or periarticular swelling can precede or accompany the skin eruption.
  • Common associations include recent streptococcal infection, sarcoidosis, tuberculosis, inflammatory bowel disease, pregnancy and selected medicines; many cases remain unexplained.
  • Bilateral hilar lymphadenopathy with erythema nodosum and ankle periarthritis forms Löfgren syndrome, an acute sarcoid phenotype with a generally favourable course.
  • First-line assessment is a focused history and examination plus FBC, inflammatory markers, throat and infection evaluation and chest imaging when the cause is not already secure.
  • Biopsy is not required for a classic self-limited presentation; an atypical distribution, ulcer, persistent single nodule or diagnostic uncertainty needs a deep incisional sample containing subcutaneous fat.
  • First-line treatment addresses the driver and uses rest, leg elevation, cool compresses and simple analgesia; an NSAID is appropriate only when renal, gastrointestinal, cardiovascular, pregnancy and IBD risk permits.

Key red flags

Unilateral rapid progression, marked systemic toxicity, fluctuance, necrosis, ulceration, calf swelling, absent pulses, severe breathlessness, immunosuppression, persistent fever, weight loss or nodules lasting beyond the expected course requires expedited alternative-diagnosis assessment.

Atypical destructive nodule

Ulceration, drainage, marked asymmetry, livedoid change, cold tissue or a persistent solitary mass argues against ordinary erythema nodosum.

Investigation priorities

01
Focused exposure and medicine historyFirst step

Prioritise the likely driver before ordering a broad low-yield panel.

Management branches

First diagnostic sequenceConfirm the nodule behaves like erythema nodosum

Tender lower-leg nodules appear over days with or without ankle symptoms.

  1. Palpate depth and borders, compare both legs and document heat, tenderness, colour, ulceration, fluctuance, pulses and calf asymmetry using photographs with consent.
  2. Ask about throat, chest, TB, bowel, pregnancy, medicine and constitutional clues and examine joints, nodes, chest and abdomen.
  3. Request FBC, inflammatory markers and chest radiography when unexplained, adding targeted throat, TB, pregnancy or bowel tests rather than a universal autoimmune screen.
First-line symptom careUnload painful inflamed septa

The presentation is typical, circulation is intact and no urgent mimic is present.

  1. Reduce prolonged standing and impact exercise temporarily, elevate legs and use cool wet compresses while maintaining gentle movement as pain permits.
  2. Offer paracetamol or a short ibuprofen course only after checking renal, ulcer, bleeding, cardiovascular, asthma, IBD and pregnancy risk.
  3. Explain the expected bruise-like evolution and review within weeks, with earlier return for ulceration, unilateral spread, respiratory decline or systemic deterioration.

Key medicines

Ibuprofen for short-term painTake 400 mg by mouth with or after food up to three times daily for the shortest necessary period, leaving at least four hours between doses and not exceeding 1200 mg daily without prescription.Avoid active peptic ulcer or bleeding, significant renal disease, NSAID-sensitive asthma and the final trimester of pregnancy; review cardiovascular, anticoagulant and interacting-drug risk and avoid during active IBD when it may worsen bowel disease.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • British Association of Dermatologists erythema nodosumUK morphology, common associations, investigations, expected course and treatment.
  • NHS sarcoidosisAccessible systemic and cutaneous sarcoid recognition, testing and treatment context.
  • NICE NG33 tuberculosis recommendationsCurrent UK TB risk assessment, testing, microbiology, notification and treatment pathways.
  • NHS ibuprofen for adultsAdult over-the-counter dose limits, administration, contraindications and adverse effects.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom