Epileptic encephalopathy associated with human herpes virus 6 (HHV-6) encephalitis after the second cord blood transplantation in a patient with pediatric acute lymphoblastic leukemia
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- KOUZUKI Kagehiro
- Department of Pediatrics, Kyoto University Hospital
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- KATO Itaru
- Department of Pediatrics, Kyoto University Hospital
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- KATO Takeo
- Department of Pediatrics, Kyoto University Hospital
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- DAIFU Tomoo
- Department of Pediatrics, Kyoto University Hospital
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- SAIDA Satoshi
- Department of Pediatrics, Kyoto University Hospital
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- UMEDA Katsutsugu
- Department of Pediatrics, Kyoto University Hospital
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- HIRAMATSU Hidefumi
- Department of Pediatrics, Kyoto University Hospital
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- WATANABE Ken-ichiro
- Department of Pediatrics, Kyoto University Hospital
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- IDE Minako
- Department of Pediatrics, Kyoto University Hospital
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- YOSHIDA Takeshi
- Department of Pediatrics, Kyoto University Hospital
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- IMAMURA Toshihiko
- Department of Pediatrics, Kyoto Prefecture University of Medicine
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- ITO Kiminari
- Department of Hematology, Shinko Hospital
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- HEIKE Toshio
- Department of Pediatrics, Kyoto University Hospital
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- ADACHI Souichi
- Department of Human Health Science, Graduate School of Medicine, Kyoto University Graduate School
Bibliographic Information
- Other Title
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- 臍帯血再移植後のHHV-6脳炎発症からてんかん性脳症を続発した小児急性リンパ性白血病
- 症例報告 臍帯血再移植後のHHV-6脳炎発症からてんかん性脳症を続発した小児急性リンパ性白血病
- ショウレイ ホウコク サイタイケツ サイイショク ゴ ノ HHV-6 ノウエン ハッショウ カラ テ ンカンショウ ノウショウ オ ゾクハツ シタ ショウニ キュウセイ リンパセイ ハッケツビョウ
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Abstract
The incidence of HHV-6 encephalitis during hematopoietic stem cell transplantation (HSCT) in children is thought to be less than that in adults and risk factors, prognosis and complications are virtually unknown. Herein, we report a pediatric case developing epileptic encephalopathy following HHV-6 encephalitis after a second cord blood transplantation (CBT). A 7-year-old boy with relapsed B-precursor acute lymphoblastic leukemia in second remission underwent CBT. However, he received a second CBT due to graft failure. On day 25 after the second CBT, he developed short-term memory defects and seizures. He was diagnosed with HHV-6 encephalitis because HHV-6 DNA was detected in his blood and cerebrospinal fluid and abnormal hippocampal signals were seen on cranial magnetic resonance imaging (MRI). After treatment with foscarnet, HHV-6 DNA levels and MRI findings improved; however, he developed epileptic encephalopathy five months after the onset of encephalitis. There are very few reports on pediatric epileptic encephalopathy associated with HHV-6 encephalitis after HSCT. Detailed studies are needed to analyze risk factors, prognosis, and complications.
Journal
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- Rinsho Ketsueki
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Rinsho Ketsueki 55 (12), 2418-2422, 2014
The Japanese Society of Hematology
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Details 詳細情報について
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- CRID
- 1390282680013736320
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- NII Article ID
- 130004920638
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- NII Book ID
- AN00252940
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- ISSN
- 18820824
- 04851439
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- NDL BIB ID
- 026007565
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- PubMed
- 25744043
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed