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Japanese

A case with unilateral anterior uveitis,diplopia, anisocoria and periarteritis nodosa Naohiko Furuyoshi 1 , Tsutomu Shimizu 1 , Ryoichi Okamura 1 , Kazunobu Sugihara 2 1Dep. of Ophthalmol., Kumamoto Univ. Med. Sch. 2The first Dept. of Intern. Kumamoto Univ. Med. Sch pp.95-99
Published Date 1985/2/15
DOI https://doi.org/10.11477/mf.1410209320
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A 32-year-old female presented with anterior uveitis in the left eye with left lateral rectus paresis. Tenderness in Achilles' tendons had been present for the past 4 weeks and led to the clinically and histologically confirmed diagnosis of periarteritis nodosa. The anterior uveitis was nongranulomatous and fibrinous. White delicate fibrinous deposits had formed on the lens surface and pupillary margin. During the course of the disease, anisocoria became apparent particularly in the dark due to suggish pupil dilatation in the left eye. Crossed immuno-electrophoresis of the aqueous showed a higher protein content in the affected than the fellow eye, indicating the anterior uveitis to be strictly unilat-eral.

Published reports on associated occurrence of anterior uveitis and periarteritis nodosa are few in number. There is no report, to our knowledge, on further association with diplopia and anisocoria.


Copyright © 1985, 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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