Makindo Medical Notes"One small step for man, one large step for Makindo" |
|
---|---|
Download all this content in the Apps now Android App and Apple iPhone/Pad App | |
MEDICAL DISCLAIMER: The contents are under continuing development and improvements and despite all efforts may contain errors of omission or fact. This is not to be used for the assessment, diagnosis, or management of patients. It should not be regarded as medical advice by healthcare workers or laypeople. It is for educational purposes only. Please adhere to your local protocols. Use the BNF for drug information. If you are unwell please seek urgent healthcare advice. If you do not accept this then please do not use the website. Makindo Ltd. |
Purpura is a sign of an underlying issue with blood vessels, platelets, or the coagulation system. The cause can range from benign conditions like minor trauma to life-threatening disorders such as DIC or leukaemia. A thorough history, physical examination, and targeted laboratory investigations are essential for diagnosing the underlying cause and guiding appropriate management.
Purpura occurs when blood leaks from small blood vessels into the skin, mucous membranes, or other tissues. The underlying causes of purpura can be categorized into:
Cause | Clinical Features | Investigations | Management |
---|---|---|---|
Immune Thrombocytopenic Purpura (ITP) |
- Easy bruising, petechiae, purpura.
- Mucosal bleeding (e.g., epistaxis, gingival bleeding). - May follow a viral infection. |
- Full blood count (FBC): Isolated thrombocytopenia (low platelet count).
- Peripheral blood smear: Normal red and white cell morphology. - Bone marrow biopsy (if needed): Normal or increased megakaryocytes. |
- Corticosteroids (first-line).
- Intravenous immunoglobulin (IVIG) for acute bleeding. - Thrombopoietin receptor agonists or splenectomy for refractory cases. |
Thrombotic Thrombocytopenic Purpura (TTP) |
- Fever, neurological symptoms, renal impairment.
- Purpura, fatigue, and pallor. - May have jaundice or signs of haemolysis. |
- FBC: Thrombocytopenia, haemolytic anaemia.
- Blood smear: Schistocytes (fragmented red cells). - ADAMTS13 activity assay: Reduced in TTP. |
- Urgent plasma exchange (plasmapheresis).
- Corticosteroids or rituximab. - Supportive care, including transfusions if required. |
Henoch-Schönlein Purpura (HSP) |
- Palpable purpura, typically on the buttocks and lower limbs.
- Abdominal pain, joint pain, and haematuria (renal involvement). - Usually affects children and may follow an upper respiratory tract infection. |
- Urinalysis: Hematuria, proteinuria.
- Renal function tests (creatinine, urea) to assess kidney involvement. - Skin biopsy (if needed): Leukocytoclastic vasculitis. |
- Supportive care: Adequate hydration, pain relief.
- Corticosteroids for severe renal or abdominal involvement. - Monitor kidney function closely in severe cases. |
Disseminated Intravascular Coagulation (DIC) |
- Widespread purpura, petechiae, and bleeding from multiple sites.
- Associated with sepsis, trauma, or malignancy. - May present with hypotension, shock, and organ failure. |
- Coagulation profile: Prolonged PT and aPTT, low fibrinogen.
- FBC: Thrombocytopenia. - D-dimer: Elevated. |
- Treat the underlying cause (e.g., sepsis, trauma).
- Blood products (e.g., fresh frozen plasma, platelets) for bleeding. - Heparin in selected cases of chronic DIC. |
Vasculitis (e.g., Small Vessel Vasculitis) |
- Palpable purpura, often on the lower limbs.
- Systemic symptoms: fever, weight loss, joint pain. - May involve the kidneys, lungs, or gastrointestinal tract. |
- ANCA (antineutrophil cytoplasmic antibodies): Positive in some vasculitides.
- Skin or renal biopsy: Evidence of vasculitis. - Renal function tests if kidney involvement. |
- Corticosteroids and immunosuppressive agents (e.g., cyclophosphamide).
- Supportive care for organ involvement. - Monitor for relapses and complications. |
Leukaemia |
- Fatigue, frequent infections, bruising, and purpura.
- Fever, weight loss, and lymphadenopathy. - Bone pain may also be present. |
- FBC: Leukocytosis or pancytopenia, thrombocytopenia.
- Bone marrow biopsy: Blasts present in acute leukaemia. - Blood smear: Abnormal immature cells. |
- Chemotherapy for leukaemia based on subtype (e.g., ALL, AML).
- Supportive care (e.g., transfusions) as needed. - Bone marrow transplant in selected cases. |
Vitamin C Deficiency (Scurvy) |
- Purpura, bruising, and gingival bleeding.
- Joint pain, corkscrew hair, and poor wound healing. - Fatigue and irritability. |
- Clinical diagnosis based on symptoms and dietary history.
- Serum ascorbic acid levels may be low. - FBC: May show anaemia. |
- Oral or intravenous vitamin C supplementation.
- Dietary advice to ensure adequate vitamin C intake. - Monitor for resolution of symptoms over time. |
Drug-Induced Purpura (e.g., anticoagulants, steroids) |
- Purpura, bruising, and mucosal bleeding.
- History of recent medication use (e.g., warfarin, steroids). - No systemic signs if drug-related. |
- FBC: May show thrombocytopenia.
- Coagulation profile: Prolonged PT or aPTT if anticoagulants are used. - Review medication history. |
- Discontinue or adjust the offending drug.
- Vitamin K or fresh frozen plasma for warfarin overdose. - Supportive care and monitor for improvement. |