Vogt-Koyanagi-Harada Disease - EyeWiki
Vogt-Koyanagi-Harada (VKH) disease is defined as a bilateral granulomatous panuveitis with or without extraocular manifestations affecting young adults. Vogt in 1906 and Koyanagi in 1929 described the same disorder independently characterized by chronic anterior uveitis, alopecia, vitiligo, and dysacusia.
Vogt–Koyanagi–Harada disease - Wikipedia
Vogt–Koyanagi–Harada disease (VKH) is a multisystem disease of presumed autoimmune cause that affects melanin-pigmented tissues. The most significant manifestation is bilateral, diffuse uveitis, which affects the eyes.
Vogt-Koyanagi-Harada (VKH) Disease - University of Iowa
2019年4月1日 · Vogt-Koyanagi-Harada (VKH) Disease is a systemic autoimmune condition characterized by bilateral non-necrotizing granulomatous panuveitis associated with extraocular integumentary changes, such as poliosis and vitiligo, and inflammation affecting the uvea, inner ear, hair, and meninges.
Identify and Treat Vogt-Koyanagi-Harada Syndrome
2005年7月1日 · Vogt-Koyanagi-Harada syndrome is an uncommon multisystem inflammatory disorder characterized by panuveitis with serous retinal detachments, and it is often associated with neurologic and cutaneous manifestations, including headache, hearing …
Vogt–Koyanagi–Harada syndrome - DermNet
Vogt-Koyanagi-Harada syndrome (VKH) is a multisystem disease that presents with a combination of ophthalmological, neurological, and dermatological signs and symptoms. The main defining clinical finding of VKH is severe bilateral granulomatous panuveitis (inflammation throughout the uveal tract in the eye).
Treatment and Prognosis of Vogt–Koyanagi–Harada Disease: …
Patients in whom VKH is suspected or diagnosed should be sent to uveitis centers for proper and prompt treatment, including, if needed, immunosuppressive therapy, periocular injections, or intravitreal implants of corticosteroids.
Evolving Understanding and Treatment of Vogt-Koyanagi-Harada …
2019年1月1日 · Vogt-Koyanagi-Harada (VKH) disease is characterized as a bilateral non-necrotizing granulomatous pan-uveitis that presents in various stages with extraocular findings.
Vogt-Koyanagi-Harada Disease: Current Diagnosis and …
2023年10月31日 · Vogt-Koyanagi-Harada (VKH) disease, formerly called as uveo-meningitic syndrome, is a systemic autoimmune disorder involving multiple organ systems, including the ocular, auditory, nervous, and integumentary. Severe bilateral panuveitis along with exudative retinal detachment is characteristic for this disease [1].
Vogt-Koyanagi-Harada Disease | SpringerLink
2 天之前 · Vogt-Koyanagi-Harada disease (VKH) is a multisystem autoimmune disorder affecting pigmented tissues such as the eye, auditory, integumentary, and central nervous systems. ... prodromal (mimics a viral infection), uveitic (bilateral diffuse uveitis with papillitis and exudative retinal detachment), convalescent (tissue depigmentation), and ...
New Perspectives on the Immunopathogenesis and Treatment of Uveitis ...
2021年11月12日 · Uveitis associated with Vogt-Koyanagi-Harada (VKH) disease is a bilateral, chronic, granulomatous autoimmune disease associated with vitiligo, poliosis, alopecia, and meningeal and auditory manifestations. The disease affects pigmented races with a predisposing genetic background.