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Ophthalmology · Uveitis: VKH syndrome
Sample itemA young Asian woman has bilateral serous retinal detachments, headache, tinnitus and later poliosis and vitiligo. What is the diagnosis?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Vogt-Koyanagi-Harada disease
VKH is an autoimmune attack on melanocytes with meningism, uveitis and later sunset-glow fundus, with poliosis, vitiligo and alopecia. High-dose steroids then immunosuppressants are used.
Option by option
A. Vogt-Koyanagi-Harada disease (correct)
Correct. Multisystem melanocyte involvement is classic.
B. Behcet disease
Behcet has oral ulcers and hypopyon uveitis.
C. Toxoplasmosis
Toxoplasmosis gives a focal retinochoroiditis.
D. Sarcoidosis
Sarcoidosis has granulomas and hilar nodes.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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