Description

The Vogt-Koyanagi-Harada (VKH) Syndrome can be diagnosed using the criteria specified by the American Uveitis Society at the 2nd Annual Meeting in Kansas City, Missouri, in 1978.


 

Criteria for the diagnosis of the Vogt-Koyanagi-Harada Syndrome:

(1) absence of previous ocular trauma or surgery

(2) at least 3 of the following:

(2a) bilateral iridocyclitis

(2b) posterior uveitis (including exudative retinal detachment or sunset glow fundus)

(2c) central nervous system problems: tinnitus, vertigo, dysacusis, meningism (with fever, headache, nausea, vomiting), cranial nerve dysfunction, cerebrospinal fluid pleocytosis

(2d) cutaneous findings: alopecia, poliosis (premature greying of the hair), vitiligo

 

Additional tests may be needed to exclude disorders in the differential diagnosis:

(1) syphilis

(2) Lyme's disease serology

(3) autoimmune disorders (ANA, RF, etc.)

(4) chest X-ray or other tests to exclude sarcoid

(5) others

 

Additional studies useful in confirming the diagnosis:

(1) fluorescein angiography

(2) HLA typing (HLA-DR4, HLA-Dw53, others)

 

Limitations:

• Patients may present with incomplete or delayed appearance of the extraocular manifestations, especially if treated early with steroids or immunosuppressive agents.

• The patterns of symptoms may vary between racial groups.

 


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