PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT

PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT

Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto blindnessanddeafness.(1) In this case, we report a 22-year-old ma...

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Veröffentlicht in:International journal of advanced research (Indore) 2023-02, Vol.11 (2), p.1257-1261
Hauptverfasser: M., Elakhdari, Y., Akannour, C., Bardi, K., Mrad, S., Hassina, L., Serghini, A., El Hassan, A., Berraho
Format: Artikel
Sprache:eng
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Zusammenfassung:Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto blindnessanddeafness.(1) In this case, we report a 22-year-old man who developed probable Vogt–Koyanagi–Haradadisease without any systemic symptoms, but with several risk factors for poor visual prognosisbeforetreatment,andwhowassuccessfullytreatedwithintensivecorticosteroidtherapy. Our aim is to describe a clinical case with bilateral serous retinal detachment that presumed asprobableVKHdisease.
ISSN:2320-5407
2320-5407
DOI:10.21474/IJAR01/16375