Purpura
Background
- Purpura results from extravasation of blood into the skin or mucous membranes
- Palpable purpura are a result of either perivascular inflammation (vasculitis) or infection
- Non-palpable petechiae usually occur in low platelet states such as ITP and DIC
- Key EM distinction: palpable (vasculitis/infection) vs. non-palpable (thrombocytopenia/coagulopathy)
- Fever + purpura in a child is meningococcemia until proven otherwise — requires emergent antibiotics
Rash Red Flags[1]
- Fever
- Toxic appearance
- Hypotension
- Mucosal lesions
- Severe pain
- Very old or young age
- Immunosuppressed
- New medication
Clinical Features
Both petechiae and purpura do not blanch with pressure (distinguishing feature from erythema)
- Purpura subdivided by size:
- <2mm of hemorrhage: petechiae
- >2mm of hemorrhage: purpura
- Large areas: ecchymoses
- Palpable purpura: raised, can be felt; indicates vasculitis or septic emboli
- Non-palpable (flat) purpura: platelet disorder, coagulopathy, or fragile vessels
Key Physical Exam Features
- Distribution: dependent areas (gravitational), generalized, or localized
- Palpability: palpable vs. non-palpable
- Associated findings: fever, arthralgia, abdominal pain, renal involvement (Henoch-Schönlein purpura / IgA vasculitis)
- Mucosal involvement: oral petechiae, gingival bleeding (suggests severe thrombocytopenia)
- Signs of systemic illness: hemodynamic instability, altered mental status
Purpural Rash
Henoch-schonlein purpura (Palpable purpura)
Neonatal purpura fulminans
Red Flags
- Fever + petechiae/purpura (meningococcemia, endocarditis, Rocky Mountain spotted fever)
- Rapidly spreading purpura (DIC, purpura fulminans)
- Platelets <10,000 (high risk of spontaneous bleeding)
- Active hemorrhage from mucosal sites
- Altered mental status with purpura (TTP — emergent plasma exchange)
Differential Diagnosis
Petechiae/Purpura (by cause)
- Abnormal platelet count and/or coagulation
- Septicemia
- Idiopathic thrombocytopenic purpura (ITP)
- Hemolytic uremic syndrome
- Leukemia
- Coagulopathies (e.g. hemophilia)
- Henoch-Schonlein Purpura (HSP)
- Acute hemorrhagic edema of infancy (AHEI)
- Hypersensitivity vasculitis
- Primary vasculitides
- Wegener's
- Microscopic polyangiitis
- Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)
- Secondary vasculitides
- Trauma
Petechiae/Purpura (by findings)
- Febrile, toxic
- Palpable
- Meningococcemia
- Disseminated gonococcal infection
- Endocarditis
- Rocky mountain spotted fever
- HSP
- Non-palpable
- Palpable
- Afebrile, nontoxic
- Palpable
- Autoimmune vasculitis
- Non-palpable
- Palpable
Evaluation
All Patients
- CBC with platelet count — most critical initial test
- Peripheral blood smear (schistocytes in TTP/HUS, blasts in leukemia)
- PT/INR, PTT (coagulopathy assessment)
- BMP (renal function — assess for HUS, TTP)
If Thrombocytopenic
- Consider DIC panel: fibrinogen, D-dimer, fibrin degradation products
- LDH, haptoglobin, reticulocyte count if concern for TTP/HUS
- Type and screen
- Consider blood cultures, lactate if febrile
If Platelets Normal
- Evaluate for coagulopathy (PT/INR, PTT)
- If palpable purpura: ESR, CRP, UA (renal involvement), complement levels (C3, C4)
- Consider skin biopsy referral (vasculitis workup)
- Blood cultures, lactate if concern for septic emboli or endocarditis
Pediatric
- For children with fever and petechiae/purpura consider using the Barts Health NHS Trust guideline for workup, which performed well in the Petechiae in Children (PiC) study[2][3]
Management
Emergent
- Meningococcemia: immediate IV ceftriaxone (do not delay for LP); fluid resuscitation
- DIC: treat underlying cause; transfuse platelets, FFP, cryoprecipitate as needed
- TTP: emergent hematology consultation for plasma exchange; do NOT transfuse platelets (can worsen)
- Severe thrombocytopenia (<10,000) with active bleeding: platelet transfusion
Condition-Specific
- ITP: if bleeding or platelets <30,000: IV dexamethasone, consider IVIG; hematology consultation
- Henoch-Schönlein purpura / IgA vasculitis: supportive care, NSAIDs for joint pain; monitor renal function
- Drug-induced thrombocytopenia: discontinue offending agent, supportive care
- HUS: supportive care, dialysis if needed; avoid antibiotics in typical (STEC) HUS
- Vasculitis: rheumatology consultation, may require immunosuppression
Disposition
Admit
- Fever with petechiae/purpura and ill appearance
- Suspected meningococcemia, TTP, HUS, DIC
- Severe thrombocytopenia (<20,000) or active bleeding
- New diagnosis requiring urgent workup (possible leukemia, aplastic anemia)
- Hemodynamic instability
Discharge
- Well-appearing child with petechiae above the nipple line (mechanical cause — coughing, vomiting), normal CBC, and no fever
- Known stable ITP with platelet count at baseline and no bleeding
- Chronic/known vasculitis with mild flare — arrange outpatient follow-up
- Return precautions: fever, spreading rash, bleeding, altered mental status, worsening symptoms
See Also
References
- ↑ Nguyen T and Freedman J. Dermatologic Emergencies: Diagnosing and Managing Life-Threatening Rashes. Emergency Medicine Practice. September 2002 volume 4 no 9.
- ↑ Thomas et al. Validating clinical practice guidelines for the management of children with non-blanching rashes in the UK (PiC): a prospective, multicentre cohort study, The Lancet Infectious Diseases, 2020, https://doi.org/10.1016/S1473-3099(20)30474-6
- ↑ Tessa Davis. Petechiae in Children – the PiC Study, Don't Forget the Bubbles, 2020. Available at: https://doi.org/10.31440/DFTB.30782
