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Toshiyuki Hikita1), Hirokazu Kutuma1), Yuko Osaka1,3), Natsue Nakamoto1),
Sono Kaneko1), Yasushi Fujii1), Yasuko Fujita1), Shigetoshi Kobayashi1), Takuya Hattori1), Hiroshi Oba2), Yukishige Yanagawa1)
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Intracranial hemorrhage is a rare but life threatening complication of childhood idiopathic thrombocytopenic purpura (ITP). The purpose of this report is to describe a case of ITP with multiple areas of intracranial hemorrhage in a 14-year-old Korean-Japanese girl.
The patient was admitted to the hospital following a sudden episode of diminished consciousness. She had a history of vomiting for one day and purpura for 18 days. On physical examination, she was confused and drowsy. Hematological examination revealed a hemoglobin of 7.4 g/dl and platelet count of 1000/μl. Computed tomography (CT) revealed multiple intracranial hemorrhages in the white matter. Initially, the patient was given 10 units of platelets, 1 g/kg of gamma globulin and 1 g of methylprednisolone intravenously, and received a second transfusion of platelets, gamma globulin and methylprednisolone the following day. Her level of consciousness rapidly progressed to normal. Her platelet count continually improved, and a tapered regiment of oral predonisolone was started at 60 mg/day. A magnetic resonance imaging (MRI) performed 15 days later showed some residual hemorrhage. A CT scan performed 5 months later showed calcification in the area of the hemorrhage.
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