Juvenile Xanthogranuloma (JXG; Nevoxanthoendothelioma) 6
General: Childhood disease; unknown etiology.
Ocular: Uveal tract tumor presenting as spontaneous hyphema; secondary glaucoma; uveitis; corneal, lid, and epibulbar tumors; proptosis; retinal and choroidal lesions (rare).
Clinical: Multiple benign tumors, primarily of the skin; usually appear in the first 3 years of life; lesions appear as yellow-to-brown papules or nodules.
DeBarge LR, et al. Chorioretinal, iris, and ciliary body infiltration by juvenile xanthogranuloma masquerading as uveitis. Surv Ophthalmol 1994; 39:65-71.
Fraunfelder FT, Roy FH. Current Ocular Therapy, 5th ed. Philadelphia: WB Saunders, 2000.
Kaufmann JG, et al. Juvenile xanthogranuloma of the corneoscleral limbus. Ophthalmic Surg 1993; 24:428-430.
Zimmerman LE. Ocular lesions of juvenile xanthogranuloma. Nevoxanthoendothelioma. Am J Ophthalmol 1965; 60: 1011-l035.
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