Literature DB >> 28548582

Bilateral Iris Depigmentation and Ocular Hypotony as End-Stage Manifestations of Untreated Vogt-Koyanagi-Harada Disease.

Miguel Cuevas1, Alejandra de-la-Torre2, Andrea Córdoba3.   

Abstract

PURPOSE: To describe severe bilateral iris depigmentation and persistent ocular hypotony as end-stage manifestations of untreated Vogt-Koyanagi-Harada disease.
METHODS: We present the clinical findings and diagnostic studies performed for three patients with bilateral iris depigmentation.
RESULTS: Vogt-Koyanagi-Harada disease in late recurrent stage was diagnosed in three patients with bilateral severe iris depigmentation and persistent ocular hypotony.
CONCLUSIONS: Early diagnosis and treatment of inflammation are crucial factors in the clinical outcome of Vogt-Koyanagi-Harada disease. When left undiagnosed and untreated from early stages, severe iris depigmentation and ocular hypotony, uncommon manifestations of this disease, can develop.

Entities:  

Keywords:  Iris atrophy; Iris depigmentation; VKH; Vogt–Koyanagi–Harada disease; ocular hypotony; panuveitis

Mesh:

Year:  2017        PMID: 28548582     DOI: 10.1080/09273948.2017.1320411

Source DB:  PubMed          Journal:  Ocul Immunol Inflamm        ISSN: 0927-3948            Impact factor:   3.070


  2 in total

1.  Bilateral Iris depigmentation, transillumination defects and hypotony in Vogt-Koyanagi-Harada disease.

Authors:  Mohit Garg; Dipankar Das; Harsha Bhattacharjee; Kanika Godani; Madhusmita Mahapatra; Riddhi Raichura
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

2.  Long-term efficacy of dexamethasone intravitreal implant in the treatment of Vogt-Koyanagi-Harada disease relapsing posterior uveitis.

Authors:  Tarek R Elhamaky
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

  2 in total

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