Immune thrombocytopenia (ITP)
Immune-mediated platelet destruction (often post-viral)
Overview
Isolated thrombocytopenia from immune platelet destruction, typically 1–2 weeks after a viral infection in an otherwise well young child. Usually self-limiting; the task is to exclude sinister causes of low platelets.
Recognise
- Sudden bruising, petechiae, mucosal bleeding (epistaxis, gums) in a WELL child
- Isolated LOW platelets — Hb and white cells normal
- No hepatosplenomegaly or lymphadenopathy (those suggest leukaemia)
Red flags
- Significant mucosal/GI bleeding; suspected intracranial bleed (severe headache/neuro signs) — rare but serious
Differentials & how to tell them apart
Investigations
FBC + blood film: isolated thrombocytopenia, otherwise normal; the film excludes blasts. Bone marrow only if atypical features or before steroids in doubt.
Management
Watchful waiting in the well child; treat bleeding, not the number
- 1If the child is well with only skin signs: watchful waiting + safety-net (avoid contact sport, NSAIDs, aspirin).Gate: Treatment (steroids/IVIG) is for significant BLEEDING, not for a low platelet count alone
- 2Significant bleeding: prednisolone or IVIG (or anti-D). Persistent >12 months = chronic ITP → haematology.
Key points
Isolated thrombocytopenia in a well child = ITP; pancytopenia or organomegaly/bone pain shifts you to leukaemia — exactly the discrimination the exam wants.
Monitor & prognosis
Platelet recovery (usually weeks); bleeding signs.
~80% of childhood ITP resolves spontaneously within 6 months.
Source: NICE CKS; British Society for Haematology