Purpura is a visible sign of an underlying problem with blood vessels, platelets, or the coagulation system. Causes range from benign trauma to life-threatening disorders like DIC or leukaemia. A good history, exam, and targeted tests are essential to identify the cause and guide management.
π£ What is Purpura?
- Petechiae: π΄ Tiny pinpoint red/purple spots (<3 mm).
- Ecchymoses: π Larger patches (>1 cm), commonly called bruises.
β Why Does Purpura Happen?
Purpura occurs when blood leaks from small vessels into the skin or mucous membranes. Key categories include:
- π©Έ Vascular causes: Vasculitis, vessel inflammation/damage.
- π§© Platelet disorders: Low platelets (ITP, TTP) or dysfunctional platelets.
- βοΈ Coagulation disorders: Factor deficiencies (e.g., DIC).
- π€ Trauma: Direct vessel injury.
- π Medications: Anticoagulants, steroids β fragile vessels/clotting issues.
π Common Causes & Features
𧬠Immune Thrombocytopenic Purpura (ITP)
- Features: Easy bruising, petechiae, mucosal bleeding (nose, gums), often post-viral.
- Investigations: FBC β isolated low platelets, smear normal, BM biopsy shows β megakaryocytes.
- Management: Corticosteroids, IVIG for acute bleeds, TPO receptor agonists/splenectomy if refractory.
β‘ Thrombotic Thrombocytopenic Purpura (TTP)
- Features: Fever, neuro symptoms, renal failure, purpura, anaemia, jaundice.
- Investigations: FBC β thrombocytopenia + haemolysis; smear β schistocytes; ADAMTS13 β.
- Management: Urgent plasma exchange, steroids/rituximab, supportive care.
πΆ Henoch-SchΓΆnlein Purpura (HSP)
- Features: Palpable purpura on buttocks/legs, abdominal pain, arthritis, haematuria (renal).
- Investigations: Urinalysis β protein/haematuria; renal tests; skin biopsy shows leukocytoclastic vasculitis.
- Management: Supportive, hydration + analgesia, steroids for severe renal/abdominal disease.
π₯ Disseminated Intravascular Coagulation (DIC)
- Features: Widespread bleeding, petechiae, purpura, shock, multiorgan failure (often in sepsis/trauma/malignancy).
- Investigations: Prolonged PT/aPTT, low fibrinogen, low platelets, β D-dimer.
- Management: Treat cause (e.g., infection), FFP/platelets, heparin in chronic DIC.
π Vasculitis (Small Vessel)
- Features: Palpable purpura, fever, weight loss, joint pain, renal/GI involvement.
- Investigations: ANCA, biopsy (skin/kidney), renal tests.
- Management: Corticosteroids, immunosuppressants (cyclophosphamide), monitor organs.
π§ͺ Leukaemia
- Features: Pallor, fatigue, infections, bruising, night sweats, bone pain, lymphadenopathy.
- Investigations: FBC β cytopenias; smear β blasts; bone marrow biopsy definitive.
- Management: Chemotherapy, transfusions, bone marrow transplant in some cases.
π Vitamin C Deficiency (Scurvy)
- Features: Purpura, gingival bleeding, corkscrew hairs, joint pain, poor healing.
- Investigations: Clinical diagnosis Β± low vitamin C levels.
- Management: Vitamin C supplementation, dietary advice.
π Drug-Induced Purpura
- Features: Purpura, bruising, mucosal bleeding; history of anticoagulant/steroid use.
- Investigations: Coagulation profile prolonged, FBC may show thrombocytopenia.
- Management: Stop offending drug, vitamin K/FFP for warfarin, supportive care.
π©Ί Clinical History Points
- Onset: sudden (infection, trauma) vs gradual (vasculitis, malignancy).
- Associated: fever, arthralgia, renal involvement, mucosal bleeding.
- Drug history: anticoagulants, steroids.
- Family history: haemophilia, vWD.
π©ββοΈ Examination
- Distribution: localised vs generalised.
- Type: petechiae vs ecchymoses vs palpable purpura.
- Systemic signs: lymphadenopathy, hepatosplenomegaly, infection signs.
π§ͺ Investigations
- FBC (platelets, anaemia).
- Coagulation profile (PT, aPTT, fibrinogen).
- Blood smear (schistocytes, blasts).
- Liver and renal function tests.
- Autoimmune markers (ANA, ANCA).
π Management Principles
- π©Έ ITP β steroids, IVIG, splenectomy if refractory.
- β‘ TTP β urgent plasma exchange + steroids.
- π₯ Vasculitis β corticosteroids + immunosuppressants.
- π DIC β treat cause, give FFP/platelets.
- π Scurvy β vitamin C replacement.
- π Drug-induced β stop drug, supportive care.