Vogt-Koyanagi-Harada (VKH) disease is a rare autoimmune disorder that affects various parts of the body, including the eyes, skin, and nervous system. Diagnosing VKH disease requires a comprehensive evaluation by a healthcare professional, typically an ophthalmologist or a rheumatologist.
Medical History: The diagnostic process usually begins with a detailed medical history. The doctor will ask about the patient's symptoms, their duration, and any previous medical conditions or treatments. This information helps to establish a baseline and identify potential risk factors.
Physical Examination: A thorough physical examination is conducted to assess the patient's overall health and identify any visible signs or symptoms of VKH disease. The doctor may examine the eyes, skin, and nervous system for any abnormalities.
Eye Examination: The eyes are a primary target of VKH disease. An ophthalmologist will perform a comprehensive eye examination, including visual acuity tests, slit-lamp examination, and fundoscopy. These tests help to evaluate the presence of inflammation, such as uveitis (inflammation of the uvea) or retinal detachment.
Lab Tests: Various laboratory tests may be ordered to support the diagnosis of VKH disease. These tests include:
Diagnostic Criteria: The International Committee on VKH Disease has established specific diagnostic criteria, which include the presence of certain clinical features and the exclusion of other conditions. These criteria help ensure an accurate diagnosis and differentiate VKH disease from other similar conditions.
It is important to note that the diagnosis of VKH disease may require multiple visits and a collaborative approach involving different specialists. Early diagnosis and treatment are crucial to prevent complications and preserve vision.