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臨床実験
8年間経過を観察した膠様滴状角膜変性症の1例とその組織所見
Gelatinous Drop-Like Corneal Dystrophy:Case Report with Histopathological Findings
進藤 晋一
Shin'ichi Shindo
pp.1167-1174
発行日 1969年10月15日
Published Date 1969/10/15
DOI https://doi.org/10.11477/mf.1410204154
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I.緒言
膠様滴状角膜変性症は,わが国の文献には30数家系,約50例が報告されているが,外国においては,わずか1,2の報告があるにすぎない。著者は約8年間にわたつて,本疾患の1例を観察し,その経過中に1眼の眼球内容除去を行ない,組織学的に検索する機会を得たのでここに報告する。
Gelatinous drop-like corneal dystrophy is not a rare occurrence in Japan with no less than 30 reported cases. Familial incidence of recessi-ve type has been observed in some of them. A report of a case is presented by the author.
The patient, now a 68-year-old Japanese male, has had no family history in particular and no, other systemic diseases except for his eye con-dition. Initial eye symptoms, which developed towards the end of the third decade of life, con-sisted of blurring of vision, foreign body sen-sation, photophobia, lacrimation and redness in both eyes.
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