Vitamin A Deficiency-induced Keratomalacia Due to Malabsorption Syndrome

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Fitri Othman
Nayan Joshi
Siti Abdullah

Abstract

Background: Keratomalacia is commonly reported in regions with high levels of malnutrition. We present a rare case of Vitamin A deficiency-induced keratomalacia due to malabsorption syndrome in Brunei Darussalam, a country with one of the highest per-capita gross domestic products in Southeast Asia - highlighting the importance of considering nutritional deficiencies even in affluent settings.
Case presentation: An 18-year-old Malay male presented with right eye redness, congestion and hand movement vision. He had atopic dermatitis, asthma, hyper Ig E syndrome, and multiple vitamin deficiencies, including vitamin D, vitamin B12, and iron. He was HLA dQ8 and DQ7 positive, DQ7 being a risk allele for coeliac disease. On initial examination, there was a right shield ulcer, which was treated for vernal atopic keratoconjunctivitis. Over a period of one month his skin and eye condition worsened, with xerosis of the conjunctiva, corneal thinning, perforation of corneal shield ulcer with an iris plug and shallowed anterior chamber. The clinical signs strongly suggest Vitamin A deficiency causing keratomalacia. He was admitted for systemic steroid treatment and given conservative intensive treatment of lubricants and topical antibiotics (moxifloxacin, tobramycin, and atropine). At six months review, and through a comprehensive treatment approach including Vitamin A supplements, carotenoid-rich food, the patient demonstrated a remarkable restoration of visual acuity of 6/9 in the affected eye.
Conclusion: Although Vitamin A deficiency is more common in developing countries, this case highlights that it can occur in a socioeconomically developed setting and may present with atypical features. Thorough history taking and clinical correlations are important to guide timely diagnosis and management in similar cases. Early recognition and prompt intervention are crucial to prevent irreversible visual loss.

Article Details

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Case Report

References

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