Is it Vogt-Koyanagi-Harada syndrome?
Vogt-Koyanagi-Harada syndrome (VKH syndrome) is named after ophthalmologists Alfred Vogt from Switzerland and Yoshizo Koyanagi and Einosuke Harada from Japan.
Digambar Dashatwar +2 more
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Vogt–Koyanagi–Harada disease recurrence after laser treatment: A case report [PDF]
This study reports two cases of Vogt–Koyanagi–Harada disease recurrence after laser treatment. Case 1 involved a woman in her late 70s with Vogt–Koyanagi–Harada disease that was controlled by adalimumab and steroid eye solution therapy.
Tetsuya Muto +4 more
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Vogt-Koyanagi-Harada Disease Exacerbation Associated with COVID-19 Vaccine
We describe a case of Vogt-Koyanagi-Harada (VKH) disease exacerbation after COVID-19 vaccination. A 46-year-old woman presented with a bilateral granulomatous uveitis 2 days after the first dose of COVID-19 mRNA vaccine (Comirnaty, Pfizer-BioNTech), and ...
Begoña De Domingo +5 more
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Vogt–Koyanagi–Harada-like uveitis with severe hyalitis during treatment by anti-programmed death 1 antibody for lung cancer: a case report [PDF]
Background Vogt–Koyanagi–Harada-like uveitis that presents with severe hyalitis has rarely been reported during anti-programmed death 1 therapy. Case presentation A 70-year-old Chinese man presented with bilateral visual disturbances and vomiting after ...
Xuanli Liu +4 more
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Acute interstitial nephritis and probable Vogt–Koyanagi–Harada disease following COVID-19 infection: a case report [PDF]
Introduction Vogt–Koyanagi–Harada disease is an autoimmune inflammatory disease characterized by bilateral serous retinal detachment, which viral infections might induce.
Nahid Aslani +5 more
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A case presentation of an IgA nephropathy patient with Vogt-Koyanagi-Harada syndrome
Background Vogt-Koyanagi-Harada syndrome is a rare disease characterized by skin and eyelash bleaching, chronic granulomatous iridocyclitis and exudative retinal detachment, and aseptic meningitis and encephalopathy.
Quan Zhang +3 more
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Vogt–Koyanagi–Harada Syndrome (VKHS): First Two Cases Reported in Pediatric Age Group in Oman
The Vogt–Koyanagi–Harada syndrome (VKHS) is a unique form of granulomatous autoimmune disease that mostly impacts the pigmented tissues of the body. The main feature is bilateral granulomatous panuveitis, which is detected on ophthalmologic examination ...
Samiya Al Hashmi +2 more
doaj +1 more source
Vogt Koyanagi Harada syndrome in a 15-year-old girl, steroids side effects and recurrences
Background. Vogt-Koyanagi-Harada Syndrome is rare in childhood and is usually seen between the 2nd and 5th decades. We present a 15-year-old girl with findings of incomplete Vogt-Koyanagi-Harada Syndrome. Case.
Gamze Yıldırım +3 more
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Background To describe a unique case of pigmented paravenous retinochoroidal atrophy that developed several years after Vogt-Koyanagi-Harada disease. Case presentation A 28-year-old woman presented with gradual vision loss in both eyes and nyctalopia for
Prithvi Ramtohul +3 more
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Azathioprine Induced Pancytopenia in a Patient with Vogt-Koyanagi-Harada Disease: A Case Report
Vogt-Koyanagi-Harada disease is a multisystem autoimmune inflammatory disorder that affects the eyes, ears, skin, and the nervous system. It is a rare disease that mainly affects Asian, Hispanic, and Middle Eastern populations.
Sagun Khatri +7 more
doaj +1 more source

