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Rash, Purpura & Dermatologic Emergencies

Rash is skin until it is sepsis, necrosis, mucosal disease, or anaphylaxis.

Your objective: explain the approach, recognize important warning signs, then test your recall.

Abbreviations explained
ACS
Acute coronary syndrome
OMI
Occlusion myocardial infarction
ECG
Electrocardiogram
PE
Pulmonary embolism
POCUS
Point-of-care ultrasound
QTc
QT interval corrected for heart rate
LBBB
Left bundle branch block
RBBB
Right bundle branch block
hs-cTn
High-sensitivity cardiac troponin
CTA
Computed tomography angiography
ICU
Intensive care unit
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The jobRash is skin until it is sepsis, necrosis, mucosal disease, or anaphylaxis.

  1. Assess illness severity, vital signs, mucosa, eyes, palms/soles, and whether lesions blanch.
  2. Separate infectious/toxic, medication-related, ischemic/necrotizing, and allergic patterns.
  3. Photograph or mark progression when appropriate; reassess rather than trusting a single examination.

Most rashes are benign, but the dangerous minority declare themselves through toxicity, nonblanching purpura, pain out of proportion, mucosal involvement, skin failure, or rapid progression.

Meningococcemia / purpura fulminans Critical

Key: Toxic patient with nonblanching petechiae or purpura: resuscitate, cultures/antibiotics per sepsis protocol, and escalate.

Necrotizing soft-tissue infection Critical

Key: Pain out of proportion, rapid progression, bullae, anesthesia, or systemic toxicity; urgent surgical review.

SJS/TEN or severe drug reaction Critical

Key: Mucosal erosions, targetoid/blistering rash, skin pain, or detachment after a medication exposure.

Anaphylaxis / angioedema Critical

Key: Skin findings plus airway, breathing, circulation, or severe GI involvement is anaphylaxis.

Cellulitis, urticaria, viral exanthem Common

Key: Treat the patient and disposition according to systemic features and progression.

Tick what your patient has — the banner updates as you go.

New drugs in the last days to weeks, immunization, infection, travel, contacts

Fever, pain, mucosal/ocular symptoms, pruritus, rapid progression

Immunosuppression, anticoagulation, animal/tick exposure, pregnancy

Vitals and toxic appearance; blanching versus nonblanching

Mucosa, eyes, palms/soles, skin tenderness, bullae, crepitus

Mark margins of suspected cellulitis; full-body examination when concern is high

Immediate

  • Sepsis workup and broad treatment when toxic or purpuric
  • Surgical consultation first when necrotizing infection is plausible

Targeted

  • CBC, renal/liver tests, coagulation, cultures when systemically unwell
  • Biopsy/dermatology and ophthalmology input for suspected severe cutaneous adverse reaction

Avoid delay

  • Do not use normal labs or imaging to rule out necrotizing infection when the examination is concerning
Medication safety reminder

Use this as a first-pass prompt; verify all medications, doses, concentrations, contraindications, weight, pregnancy status, and local protocols before administration.

Check indication, allergy, route, renal/hepatic risk, interactions, monitoring, and local formulary.

Discharge

  • Clearly benign, stable rash with explicit return precautions and follow-up.

Admit / specialty review

  • Extensive cellulitis, immunocompromise, diagnostic uncertainty, mucosal disease, or failed outpatient treatment.

Resuscitation / OR / burn-level care

  • Sepsis/purpura, necrotizing infection, anaphylaxis, or extensive SJS/TEN.

Use objective reassessment and the local pathway.

Before the next decision · reassess and hand over

Use these learning prompts with the presentation’s pathway. They are not discharge criteria.

  1. Reassess: compare symptoms, observations and examination with the initial assessment and response to treatment.
  2. Warning signs for Rash, Purpura & Dermatologic Emergencies:
    • Nonblanching purpura with fever or shock
    • Painful, rapidly spreading, anesthetic, bullous, or necrotic skin
    • Mucosal or ocular involvement
    • Facial/tongue swelling, wheeze, hypotension
    • New high-risk medication with skin pain or blistering
  3. Reconsider: check unresolved findings and alternative explanations, including the pitfalls below.
  4. Escalate: communicate deterioration, uncertainty or needs beyond the current setting.
  5. Plan the transition: identify outstanding results, responsibility for follow-up, patient understanding and specific return advice.
Review this presentation’s disposition pathway →Practice a handover →

Clinical Pearls

  • Nonblanching plus toxic is a sepsis emergency until proven otherwise.
  • Skin pain is a higher-risk clue than itch.

Pitfalls

  • Calling painful skin disease simple cellulitis without considering necrosis or drug reaction.
  • Ignoring eye and mucosal examination in blistering disease.
PRACTICE REFRESHER

Rapid recall

Test your first action and the dangerous diagnoses before revealing the answer.

01 · First move

Before you scroll, what needs to happen first?

02 · Immediate threats

Name at least two diagnoses that cannot wait.

PRIVATE TO THIS DEVICE

Your learning note

Capture a weak point, a teaching pearl, or a question to take to your next shift.

Review schedule starts when marked reviewed

Foundational references below. No separate topic-specific guideline check is recorded here.

  • Rosen’s Emergency Medicine, 10th ed. — dermatologic presentations
  • IDSA skin/soft-tissue infection guidance; local burn/dermatology pathways