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Klin Monbl Augenheilkd 2013; 230(4): 346-348
DOI: 10.1055/s-0032-1328375
DOI: 10.1055/s-0032-1328375
Der interessante Fall
Ligneous Conjunctivitis in a Young Patient with Homozygous K19E Plasminogen Gene Mutation: a Diagnostic and Therapeutic Challenge
Conjunctivitis lignosa bei einer jungen Patientin mit homozygoter K19E-Mutation im Plasminogen-Gen: eine diagnostische und therapeutische HerausforderungFurther Information
Publication History
Publication Date:
29 April 2013 (online)
Background
Ligneous conjunctivitis is a chronic disease that may be triggered by ocular trauma or surgery in patients with type I plasminogen deficiency [1], [2]. In a recent review of the literature, the prevalence of type-I plasminogen deficiency is only 16 cases per 1 000 000 [1]. The hallmark of ligneous conjunctivitis is the presence of fibrin-rich pseudomembraneous lesions on tarsal conjunctivae.
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References
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