Pediatric uveitis.
Tugal-Tutkun I -Journal of ophthalmic & vision research(2011)
f2-jovr_v06_no4_07:Diffuse illumination at the slit lamp shows severe band keratopathy in the left eye of a boy with JIA-associated anterior uveitis.
View Article:PubMed Central - PubMed
Affiliation:Department of Ophthalmology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Additional Figures:
Article
Collection
Results
Bottom Line:Therefore, the diagnosis is often delayed and severe complications may be seen at the time of initial visit.Young children may not be cooperative for a complete ocular examination and subtle findings of intraocular inflammation such as trace cells may be easily missed in the early stages of the disease.Children, in general, tend to have more severe and chronic intraocular inflammation that frequently results in ocular complications and visual loss.
Abstract
Uveitis is less common in children than in adults, and its diagnosis and management can be particularly challenging. Young children are often asymptomatic either because of inability to express complaints or because of the truly asymptomatic nature of their disease. Even in advanced cases, parents may not be aware of severe visual impairment until the development of externally visible changes such as band keratopathy, strabismus, or leukocoria. Therefore, the diagnosis is often delayed and severe complications may be seen at the time of initial visit. Young children may not be cooperative for a complete ocular examination and subtle findings of intraocular inflammation such as trace cells may be easily missed in the early stages of the disease. Children, in general, tend to have more severe and chronic intraocular inflammation that frequently results in ocular complications and visual loss. In children who present with amblyopia or strabismus, a careful examination is required to rule out uveitis as an underlying cause. Delayed and variable presentations cause a distinct challenge in the diagnosis of uveitis in children, furthermore differential diagnosis also requires awareness of etiologies which are different from adults. There are unique forms of uveitis and masquerade syndromes in this age group, while some entities commonly encountered in adults are rare in children.
Mentions
JIA-associated anterior uveitis is typically bilateral, nongranulomatous, and has a chronic relapsing course. However, a granulomatous disease does not exclude the diagnosis (Fig. 1). Mutton-fat keratic precipitates (KPs) or iris nodules, reminiscent of sarcoidosis, have been reported in 24% of white and 56% of non-white patients.23 The most common complications of JIA-associated anterior uveitis include band keratopathy (Fig. 2), cataract, posterior synechiae (Fig. 3), glaucoma, maculopathy, hypotony and amblyopia.24,25 In a recent study, 84% of eyes with JIA uveitis were found to have maculopathy on optical coherence tomography.26 The presence of complications at the time of initial visit and high anterior chamber flare values by laser flare photometry are risk factors for development of new complications and poor visual prognosis.25,27,28 Early development of cataract requiring surgery has been associated with the presence of posterior synechiae at the time of diagnosis.29 Early immunomodulatory treatment reduces the risk of ocular complications and visual loss.24,25,29 Since high anterior chamber flare is associated with an increased risk of visual loss independent of anterior chamber cells,28 children with high flare should be treated aggressively with the aim of reducing flare to the minimum possible level.
MeSH