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Retinal vasculitis associated with human Tlymphotropic virus type I myelopathy (HAM) Kiwamu Sasaki 1 , Iori Morooka 1 , Hajime Inomata 2 , Nobuyuki Kashio 3 , Toshihiko Akamine 3 , Mitsuhiro Osame 4 1Dept of Ophthalmol, Miyazaki Prefect Hosp 2Dept of Ophthalmol, Fac of Med, Kyushu Univ 3Dept of Neurol, Miyazaki Prefect Hosp 4Third Dept of Intern Med, Fac of Med, Kagoshima Univ pp.376-380
Published Date 1989/3/15
DOI https://doi.org/10.11477/mf.1410210672
  • Abstract
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Human T-lymphotropic virus type I (HTLV-Ⅰ) has recently be found to be associated with a chronic slowly progressive myelopathy. No instance of retinal vasculitis has been known in these patients. We evaluated 12 patients with HTLV-Ⅰ associated myelopathy (HAM).

We detected vitreous opacity in 5 patients, of which retinal vasculitis was present in 3. All the 3patients were females, aged 49, 50, 58 years respec-tively. We could rule out other diseases as causes for the retinal vasculitis. Retinal vasculitis was present bilaterally in 1 and unilaterally in 2 patients. Periphlebitis was the predominant feature of retinal vasculitis, appearing as sheathing of veins in the peripheral retina. Retinal hemorrhage, exudate or necrosis was consistently absent. Involvement of the anterior segment was minimal.

Systemic corticosteroid was beneficial for the neur-ological signs, but the retinal vasculitis persisted in 2 patients. One patient was treated with interferon to relieve myelopathy. Retinal vasculitis disappear-ed following the treatment.


Copyright © 1989, 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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