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Clinical features of HLA-B27-positive uveitis Satoshi Kotake 1 , Shigeaki Ohno 1 , Shinichi Aso 1 , Atsushi Yoshida 1 , Makoto Higuchi 1 , Hidehiko Matsuda 1 1Dept. of Ophthalmol, Hokkaido Univ Sch of Med pp.589-592
Published Date 1986/6/15
DOI https://doi.org/10.11477/mf.1410209737
  • Abstract
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We detected 13 cases with HLA-B27 tissue type out of a series of 450 patients with various types of uveitis. These 13 cases consisted of 4 cases with Behget disease, 5 with ankylosing spondylitis and 4 with acute anterior uveitis of unidentified etiology. Two cases with Behçet disease also manifested ankylosing spondylitis. All the 9 non-Behçet cases were males and manifested acute anterior uveitis. They were further characterized by unilateral involvement, frequent attacks, tendency to form hypoypon and fibrinous exudation in the anteior chamber, absence of larger peratic precipitates, and tendency to form posteior synechia. Severe complica-tions were rare, resulting in favorable prognosis. There was no difference in the clinical manifestation of acute anterior uveitis whether associated with or without ankylosing spondylitis.

We compared the 9 cases with positive HLA-B27 and acute anteior uveitis with 20 cases with negative HLA-B27 and acute anterior uveitis. The HLA-B27-positive cases were characterized by a larger predominance of males, younger age of onset, and a higher rate of recur-rence.

Rinsho Ganka (Jpn J Clin Ophthalmol) 40(6) : 589-592,1986


Copyright © 1986, 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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