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Retinal vasculitis developed in a case with Hodgkin disease and aortitis syndrome Koji Hirano 1 , Takashi Harada 2 , Mika Niwa 1 , Megumi Ishikawa 1 , Ayumi Kamiya 1 , Kazumasa Yamada 3 1Dept of Ophthalmol, Nagoya Univ Sch of Med 2Dept of Ophthalmol, Nagoya Univ Branch Hosp 3Dept of Inter Med, Nagoya Univ Branch Hosp pp.889-892
Published Date 1988/7/15
DOI https://doi.org/10.11477/mf.1410210478
  • Abstract
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A 17-year-old male was diagnosed as Hodgkin disease after surgery for mediastinal tumor 4 years before. He has been under chemotherapy since. Extensive attenuation of femoral arteries were detected 3 years before and led to the diagnosis of aortitis syndrome. He was referred to us on account of gradually failing visual acuity.

The fundus picture was dominated by pigment-laden, perivascular sheathing, associated by dis-seminated, small chorioretinal atrophic patches. Both eyes were involved. Fluorescein angiography showed absence of dye leakage from the sheathed vessels. We suspected opportunistic viral infection in the pathogenesis of the fundus lesions, although peripheral blood tests were negative for herpes simplex virus, herpes zoster virus, or cytomegalovirus. The fundus findings are almost stationary during the consequent one-year follow -up period.

Rinsho Ganka (Jpn J Clin Ophthalmol) 42(7) : 889-892, 1988


Copyright © 1988, 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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