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Three Pediatric Cases with Choroid Plexus Papilloma in the Fourth Ventricle Shingo FUJIO 1 , Hirofumi HIRANO 1 , Hiroto KAWANO 1 , Ryosuke HANAYA 1 , Tatsuki OYOSHI 1 , Masaki NIIRO 2 , Kazunori ARITA 1 1Department of Neurosurgery,Graduate School of Medical and Dental Sciences,Kagoshima University 2Department of Neurosurgery,Imamura Byoin Bunin Hospital Keyword: choroid plexus papilloma , fourth ventricle , child , diffusion-weighted image pp.149-155
Published Date 2010/2/10
DOI https://doi.org/10.11477/mf.1436101108
  • Abstract
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 Choroid plexus papillomas are rare; they comprise less than 1% of all intracranial tumors. In children, most of these neoplasms arise in the lateral ventricle while in adults they are primarily located in the fourth ventricle. We report 3 children with choroid plexus papilloma in the fourth ventricle; they were one 5-month-old girl and 2 boys aged 8-and 15-years.

 The baby girl presented with macrocephaly and signs of raised intracranial pressure, the 2 boys exhibited cerebellar signs. On magnetic resonance imaging (MRI) the tumors were well-enhanced with a cauliflower-like contour and hydrocephalus. In one case, diffusion weighted images (DWIs) showed an isointense tumor signal clearly different from the well-known hyper-intensity of medulloblastomas. Via suboccipital craniotomy we succeeded in the total or subtotal surgical resection of these tumors and there were no sequela. None of the tumors have recurred in the intervening 2-9 years. In conclusion, choroid plexus papilloma should be included as a differential diagnosis in children presenting with tumors in the fourth ventricle. The contour of the tumor on MRI and its intensity on DWI may be clues for a correct preoperative diagnosis.


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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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