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ADRENAL SCHWANNOMA IN CHILD:A CASE REPORT Shinichi Nezasa 1 , Masanobu Horie 1 , Satoru Kobayashi 1 , Takashi Shinoda 1 , Osaaki Andou 2 , Kouji Konno 2 1Urology, Daiyuukai Daiichi Hospital 2Pediatrics, Daiyuukai General Hospital Keyword: 副腎腫瘍 , 神経鞘腫 pp.963-965
Published Date 1992/11/20
DOI https://doi.org/10.11477/mf.1413900738
  • Abstract
  • Look Inside

A 14-year-old girl with abdominal pain was found to have a left retroperitoneal mass on CTscan. An adrenal tumor was suspected with further study by MRI and angiography. The removed tumor (115 g in weight and 75 x 55 x 50 mm in size) was firm but elastic in consistency. The cutsurface was homogenously milky white in color. Microscopic examination confirmed the diagnosis of Schwannoma (Antoni A type) originating from the adrenal gland. This type of tumor has been considered to be rare and only four cases have been reported in Japan. To our knowledge, this is the first child case.


Copyright © 1992, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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