Summary
The present paper records the case of a young man, aged 19, with influenza followed suddenly by a Cogan-I-syndrome. The corneal infiltrations recede after local treatment with prednisolone, an effect which cannot be observed at the beginning of the disease under the same therapy. At the end of the illness only a few corneal alterations are detectable. Both vestibula are inactive, the patient remains deaf except for residual hearing on the left side.
Possible causes of the syndrome are discussed with the aid of the available literature, and diseases with similar symptomatology are mentioned.
Zusammenfassung
Es wird über einen 19jährigen Mann berichtet, der nach einem grippalen Infekt überraschend an einem Cogan-I-Syndrom erkrankte. Die cornealen Infiltrate bilden sich nach einer lokalen Prednisolon-Behandlung weitgehend zurück, ein Effekt, der zu Beginn der Erkrankung nicht beobachtet werden kann. Am Ende der Erkrankung sind noch geringe Hornhautveränderungen nachweisbar, beide Vestibulae sind unerregbar, bis auf ganz schwache Hörreste links bleibt der Patient taub.
Es werden anhand der vorliegenden Literatur mögliche Ursachen der Erkrankung diskutiert und Krankheiten mit einer ähnlichen Symptomatologie erwähnt.
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Seel, J. Cogan-I-syndrome interstitial keratitis with sudden deafness. Albrecht v. Graefes Arch. klin. exp. Ophthal. 185, 281–287 (1972). https://doi.org/10.1007/BF00410759
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DOI: https://doi.org/10.1007/BF00410759