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A case of granular cell tumor of the orbit Keisuke Kawana 1 , Harumi Nose 2 , Sachiko Honmura 2 1Dept of Ophthalmol, Tsukuba Univ Hosp 2Dept of Ophthalmol, Inst of Clinical Med, Univ of Tsukuba pp.1497-1501
Published Date 2002/9/15
DOI https://doi.org/10.11477/mf.1410907952
  • Abstract
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A 52-year-old male presented with vertical diplopia. He had noticed a hard mass in the lower margin of the orbit 2 months before. He showed no abnormal findings except the orbital tumor and intraocular pressure of 24mmHg in his right eye. Computerized tomography (CT) and magenetic resonance imaging (MRI) showed a tumor inferior to the right eyeball. Calcification or bone destruction was absent. MRI imaging of the tumor showed intermediate intensity on T1-weighted image and low intensity on T2-weighted image.The tumor showed slight enhancement with gadolinium-DTPA. Surgery showed a hard tumor mass measur-ing 20mm×12mm×12mm in size. By histopathology, the tumor cells had abundant cytoplasm and eosino-philic granules. The tumor was diagnosed with granular cell tumor, which is a rare occurrence in the orbit, af-ter immuohistologic studies showed positive for S-100 protein.


Copyright © 2002, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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