Results 1 to 10 of about 4,988,152 (170)

Vogt‐Koyanagi‐Harada disease‐like uveitis induced by nivolumab in metastatic renal cell carcinoma [PDF]

IJU Case Reports
Introduction Nivolumab can cause various immune‐related adverse events; it rarely induces Vogt‐Koyanagi‐Harada‐disease‐like uveitis. Vogt‐Koyanagi‐Harada‐disease is reported to be closely associated with human leukocyte antigen‐DR4.
Hitomi Imai, Tomoyuki Koguchi, Yuki Harigane, Kei Yaginuma, Satoru Meguro, Seiji Hoshi, Junya Hata, Hidenori Akaihata, Soichiro Ogawa, Yoshiyuki Kojima   +9 more
doaj   +3 more sources

Vogt–Koyanagi–Harada disease recurrence after laser treatment: A case report [PDF]

Journal of International Medical Research
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, Masaaki Sakamoto, Shigeki Machida, Shinichiro Imaizumi, Tetsuju Sekiryu   +4 more
doaj   +2 more sources

Vogt-Koyanagi-Harada Disease Exacerbation Associated with COVID-19 Vaccine

Cells, 2022
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, Miguel López, Maria Lopez-Valladares, Esperanza Ortegon-Aguilar, Bernardo Sopeña-Perez-Argüelles, Francisco Gonzalez   +5 more
doaj   +2 more sources

Acute interstitial nephritis and probable Vogt–Koyanagi–Harada disease following COVID-19 infection: a case report [PDF]

Journal of Medical Case Reports
Introduction Vogt–Koyanagi–Harada disease is an autoimmune inflammatory disease characterized by bilateral serous retinal detachment, which viral infections might induce.
Nahid Aslani, Mohammad Malekahmadi, Alireza Merrikhi, Alaleh Gheisari, Aida Mardani, Kimia Afshar   +5 more
doaj   +2 more sources

Systemic bias in medical consensus: how flawed panels and lack of evidence can distort definitions and guidelines: the case of Vogt-Koyanagi-Harada disease [PDF]

Journal of Ophthalmic Inflammation and Infection
Background The creation of diagnostic criteria for a disease is always challenging in medicine. Consensus meetings and expert’s opinions are sometimes responsible for establishing useful and precise diagnostic criteria but, unfortunately, not all the ...
Carl P. Herbort, Ioannis Papasavvas, Ahmed M. Abu El-Asrar, Abdulrahman F. AlBloushi, De-Kuang Hwang, Vania Lages, Wen-Jung Lo, Kazuich Maruyama, Piergiorgio Neri, Masaru Takeuchi, Yoshihiko Usui   +10 more
doaj   +2 more sources

Vogt‐Koyanagi‐Harada disease in pregnancy: Case report and review of 32 patients in the literature [PDF]

Clinical Case Reports
Key Clinical Message Systemic prednisolone including steroid pulse therapy would be safe in 32 pregnant women, who developed Vogt‐Koyanagi‐Harada disease in the literature.
Toshihiko Matsuo, Kasumi Takahashi, Tsunemasa Kondo   +2 more
doaj   +2 more sources

Atypical presentation of acute retinal necrosis mimicking Vogt-Koyanagi-Harada disease leading to misdiagnosis: a case report [PDF]

Frontiers in Medicine
Acute retinal necrosis (ARN) is a serious, sight-threatening condition characterized by rapidly progressive necrotizing retinitis, most commonly caused by varicella-zoster virus and herpes simplex virus. We report an atypical case of ARN in a 57-year-old
Wei Zhu, Cuiyun Yu, Qianqian Guo, Qingran Kang, Xusheng Cao   +4 more
doaj   +2 more sources

Vogt–Koyanagi–Harada Syndrome (VKHS): First Two Cases Reported in Pediatric Age Group in Oman

Case Reports in Pediatrics, 2023
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, Nasra Al Habsi, Safiya Al Abrawi   +2 more
doaj   +1 more source

Vogt Koyanagi Harada syndrome in a 15-year-old girl, steroids side effects and recurrences

The Turkish Journal of Pediatrics, 2021
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, Cemal Çavdarlı, Emine Yıldız Özdemir, Mehmet Numan Alp   +3 more
doaj   +1 more source

Azathioprine Induced Pancytopenia in a Patient with Vogt-Koyanagi-Harada Disease: A Case Report

Journal of Nepal Medical Association, 2022
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, Saugat Khatri, Sachit Regmi, Sulav Pyakurel, Sanjeet Bhattarai, Pankaj Barman, Dilasha Manandhar, Abhi Kumar Singh   +7 more
doaj   +1 more source