Journal of Acute Disease (Jan 2013)

A case of immune thrombocytopenic purpura presenting with intracranial hemorrhage

  • Sinan Akbayram,
  • Fesih Aktar,
  • Cihangir Akgün,
  • Mehmet Selçuk Bektaş,
  • Hüseyin Çaksen,
  • Ahmet Faik Oner

DOI
https://doi.org/10.1016/S2221-6189(13)60138-9
Journal volume & issue
Vol. 2, no. 3
pp. 250 – 251

Abstract

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Immune thrombocytopenic purpura is an acute, generally considered a self-limiting benign disorder with a 60%-80% change of spontaneous recovery occurring usually within a few months after onset. Intracranial hemorrhage is a rare but life-threatening complication of childhood immune thrombocytopenic purpura. We report a 4-year-old girl who admitted with headache, vomiting, bleeding from noise and bruises on the extremities. Her neurological examination was normal. Based on laboratory finding she was diagnosed immune thrombocytopenic purpura and intracranial hemorrhage. We suggest that cranial imaging should be perform in patients with immune thrombocytopenic purpura admitted with bleeding symptoms, vomiting and headache even if they had no abnormal neurological signs.

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