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Fuch,s Heterachromic Uvitis
K.Nasrollahi MD Feiz Hospital 1390
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-Accounting for up to 5% of uveitis in some populations
-First time was described in 1906 in a group of 38 patients by Dr.Ernest fuchs, -Accounting for up to 5% of uveitis in some populations - Its cause remain unknown
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- The epidemiology suggests that this is a purely ocular disorder
- But occasional is associated with parry romberg syndrome of hemifacial atrophy - It has been suggested that toxoplasmosis maybe linked to some cases of F.H.U
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- F.H.U is characteristically unilateral - The incidence of Bil disease is 8% - Most cases present in early adulthood but congenital heterochromia & childhood onset also reported .
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- The most common reason for presentation is floaters (because of vit opacification) - Heterochromia - Ocular discomfort - Chronic intermitent periocular pain & headache
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- Cilliary injection and ant
- Cilliary injection and ant.uveitis usually are not present but may by seen occasionally - Mild presence of cell & flare in AC - KP are typically numeroces -Moderate in size , transluscent and greyish - Scattered over the whole corneal endothelium
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- Mutton fat kps , finekps – inferior spindle are not features of F. H
- Mutton fat kps , finekps – inferior spindle are not features of F.H.U and should suggest another diagnosis.
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- Iris nodules are an important feature - F. H
- Iris nodules are an important feature - F.H.U is probably the most common cause of iris nodules - They are most prominent on the pupillary side of the colarete - Small , domed and Traslucent .
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- Heterochromia being only end – stag manifestation of F.H.U
- The Heterochromia is the most well-known feature of F.H.U - Heterochromia being only end – stag manifestation of F.H.U - Is due to atrophic changes & depigmentation of ant surface & stroma of iris
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- In some cases stromal atrophy becomes profound allowing visualization of the brown pigmented epitheliun from the ant aspect which is called inverse heterochromia
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- Post synechia are not seen in F. H
- Post synechia are not seen in F.H.U (rares) - Sometimes dilation of the pupil will reveal radial smears of iris pigment on the anterior lense surface.
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An abnormality of antrior segment vasculature is an important feature
- Vascular fragibility and an increased tendency to bleed - Minor bleeding in to the AC angle (Amsler,s sign) is a constant accompaniment to intraoculr surgery. - Recurrent hyphema is occasionally recorded
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- Occasionally minor trauma such as eye rubbing may cause microscopic hyphema - More rarely significant vitreons hemorrhage has been observed.
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- Rarely iris neovascularization is seen -AC angle rubeosis may be seen that should be diagnosed from normal iris vessel after iris atrophy. - A few eyes have been enucleated because of neovascular glaucoma in F.H.U - It is interesting that no evidence of post – segment ischemia seems to accompany such chenges
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Glaucoma - Is the most problematic feature of F.H.U - It is common = ¼ of cases. - It is usually present when the pt . Presents to ophthalmologist. - The most likely percipitant being cataract surgery - Is responsive to mepdical TX - Only a minority require surgical drainage
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Cataract P.S.C can be expected in great majority of patient with F.H.U
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Vitreous opacification
- It can be highly significant - Opacities are usually wide spread & fibrillary - Small inferier snow balls may be seen - Parsplana exudate is not seen - In some pts vitrectomy may be necessary after cat ext.
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Macular Edema - Is rare in F.H.U ever after cat,xt - In some cases its presence serves to diffrentiate F.H.U from intermediate uveites
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- It has been suggested that toxo may be the cause in some cases
- Focal choryoretinal scarring or macular scar suggest previous toxoplasma infection - It has been suggested that toxo may be the cause in some cases
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Dingnosis -The etiology of F.H.U is unknown - There is no diagnostic test - Diagnosis is mostly clinical - Bilateral cases requires a more careful observation
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Diff Dingnosis - Posner – schlossman syndrome causing heterochromia and glaucoma with mild uveitis - Unilateral intermediate uveitis may cause heterochromia
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Management - The frequent misdiagnosis of F.H.U lead to the automatic use of topical steroid XT - This may lead to cat & glaucoma formation - It is better to use topical steroids only in specific situations such as: 1- Dense accumulation of KPS 2- Percipitates on the post lense surface 3- In the cases with flare – unps of inflamation 4- At the time of intraocular surgery
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Management of cataract
-The majority of pts with F.H.U require cat ext - Most often in 4th to 5th decade - Phaco IOL ( intra bag ) is the best method
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- Topical steroids from 2 weeks preop Q6h - After operation Q2h for first few dayes - Periocular steroid injection at the time of surgery - Continue topical steroid at least 3 wks postop Q6h
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Management of glaucoma
- Medical TX of glaucoma is the first choice - Some pts reuire drainage surgery - It is better to combine surgery with antimetabolites
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