Immune thrombocytopenic purpura and intracranial haemorrhage: A formidable medical challenge

Introduction:To discuss the thought-provoking and difficult clinical management of a case of spontaneous intracerebral haemorrhage and immune thrombocytopenic purpura (ITP).Case presentation: A 6-year-old female, known ITP, presented with a one-day history of traumatic dislodged tooth, with associated neurological symptoms.However, her neurological status was alert and oriented, with absence of focal deficits.The complete blood count showed a platelet count of 26 x 10 9 /L and was in keeping with her known baseline platelet level.Computed tomography of the brain demonstrated three sites of cerebral contusions with no associated midline shift.Hours after admission, there was progressive decline in the patient's clinical status.Additionally, repeat blood investigations showed a downward trend in platelet counts.Aggressive medical management was implemented with the aid of neurosurgery, haematology, paediatrics, and the intensive care unit.Despite various therapeutic modalities, the patient succumbed to her underlying disorder.Conclusion: On retrospective review, this patient had a severe phenotype of ITP.This was demonstrated by repeated oral mucosa bleeds, gastrointestinal bleeds and episodes of haematuria preceding this last admission.Despite multimodal therapies and the combined efforts of a multi-disciplinary team, the clinical management remained arduous.