First report of keratitis in familial cold autoinflammatory syndrome

Abstract Objective To report corneal manifestations of familial cold autoinflammatory syndrome (FCAS) for the first time. Design small case series Participants Medical records of three members of a single family were reviewed after obtaining institutional review board (IRB) approval and informed con...

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Bibliographic Details
Published inCanadian journal of ophthalmology Vol. 49; no. 3; pp. 304 - 306
Main Authors Espandar, Ladan, MD, MS, Boehlke, Christopher S., MD, Kelly, Michael P., CPT
Format Journal Article
LanguageEnglish
Published England Elsevier Inc 01.06.2014
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Summary:Abstract Objective To report corneal manifestations of familial cold autoinflammatory syndrome (FCAS) for the first time. Design small case series Participants Medical records of three members of a single family were reviewed after obtaining institutional review board (IRB) approval and informed consent. Methods All three members presented with a long history of maculopapular rash after cold exposure starting in childhood associated with nausea, low-grade fever, fatigue and arthralgia that lasted less than 24 hours. Their ocular manifestations consisted of ocular pain, photophobia and keratitis with subsequent stromal haziness. Results Patients underwent systemic therapy with canalinumab (Ilaris). They responded very well to repeated injections of Ilaris without side effects. Conclusions FCAS causes lifelong debilitating effects that restrict patients’ daily activities. Ilaris is an FDA-approved treatment for this condition and that typically results in dramatic improvement in clinical and laboratory measures of inflammation, and is well tolerated. Our report is the first small case series of FCAS with keratitis that responded to Ilaris beautifully.
Bibliography:ObjectType-Case Study-2
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ISSN:0008-4182
1715-3360
DOI:10.1016/j.jcjo.2014.01.007