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A Case of Cerebral Juvenile Pilocytic Astrocytoma:Obervation of the Development of the Tumor Kazuhiko Sugiyama 1 , Kaoru Kurisu 1 , Kazunori Arita 1 , Shinji Ohba 1 , Tatsuya Mizoue 1 , Kunyu Harada 1 , Takashi Sadatomo 1 , Hiroyuki Yoshioka 1 , Seishi Hama 1 , Tohru Uozumi 2 1Department of Neurosurgery, Hiroshima University School of Medicine 2Hiroshima Prefectural Hospital Keyword: juvenile pilocytic astrocytoma , cerebral hemisphere , growth rate pp.149-153
Published Date 1999/2/1
DOI https://doi.org/10.11477/mf.1406901396
  • Abstract
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A case with cerebral juvenile pilocyticastrocytoma (JPA) was reported. The patient was 33-month-old boy, who developed headache and loss of activity on December, 1994. Although he was indicated macrocephaly at the age of just 1 year, CT scan showed no abnormality at that time. On admis-sion, MRI revealed multiple large cysts with an enhanced mural nodule in the left frontal lobe. The tumor was totally removed, and histologically diagnosed as JPA, because of alternating two types of structures of loose knit tissue composed of satel-lite astrocytes and compact tissue consisting of highly fibrillate cells.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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