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The Medical Journal of Malaysia ; : 288-290, 2014.
Artigo em Inglês | WPRIM | ID: wpr-630509

RESUMO

Spontaneous intracranial haemorrhage (ICH) is a rare complication of chronic immune thrombocytopenic purpura (ITP) in children. We report four patients with cITP who developed ICH. The latency between onset of ITP and ICH varied from 1-8 years. All our patients were profoundly thrombocytopenic (platelet count of <10 x 109/l) at the time of their intracranial bleed. The presenting features and management are discussed. All patients survived, three had complete neurological recovery while one had a minimal residual neurological deficit. KEY WORDS: Chronic immune thrombocytopenic purpura; intracranial haemorrhage; children

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