Simple Uveitis
· Mohamed Zaky Elkadim
· Tanta University
‫الرحيم‬ ‫الرحمن‬ ‫هللا‬ ‫بسم‬
ANTERIOR UVEITIS
1) Retro corneal granuloma
2) Acute severe with fibrinous reaction and pain (angry
eye)
3) Uveitic glaucoma / White and quiet
4) Granulomatous anterior uveitis
5) Behcet’s disease
1) RETRO CORNEAL
GRANULOMA
Trematode
· History of canal water contact
· Topical and systemic steroids
· TB should be excluded 1st
· Surgical excision of granuloma rarely
used.
· ± shistofast
· ± Verm-1 tab 1 tab / week *2
· ± Ca++
2) ACUTE SEVERE WITH
FIBRINOUS REACTION AND
PAIN (ANGRY EYE)
HLA B27
· The most common anterior uveitis 50%
· May be associated with “seronegative spondylo
arthropathies”: Reiter, Ankylosing spondylitis, psoraisis,
IBD.
· Not common in non whites
· Severe pain , injection , fibrinous reaction , posterior
synechiae
· Bacteria such as C hlamydia, Salmonella, Yersinia, and
Shigella have been associated.
If indicated:
· MR I : sacroiliac join and lumbar spine
· Swab or chlamydia, Shigella, Yersinia,
· No KPs : just dusting
· Pain on accomodation (pain may precede
the attack).
· Usually bilateral assymmetric and recur
causes
1. Idiopathic (1% of HLAB27 will have uveitis).
2. Ankylosing spondylitis : MRI back : most
common cause of AAU in male.
3. IBD : investigate for Calprotectin Sulfasalazine
4. Reiter : Azithromycin single dose ,, urine
and conj swab ( Urethritis →
conjunctivitis→ arthritis → uveitis)
5. Psoraisis → 20% arthritis → 20% AAU ,,
bilateral simultaneous
6. Bacterial infection trigger
3) UVEITIC GLAUCOMA /
WHITE AND QUIET
PIOL
POSNER-SCHLOSSMAN
SYNDROME (glaucmato cyclitic crisis)
· Male ,, unilateral uveitic glaucoma
· CMV
· Central white KPs with variable size
· No synechie no vitritis no heterochromia
· Between attacks : only optic cup
FUCHS’ IRIDOCYCLITIS
· Floaters are he main complain
· Rubella
· FUS is a chronic, anterior, granulomatous
with vitreous involvement .
· unilateral (90% of cases)
· ciliary injection and posterior synechiae are
never present and should be viewed as exclusion
criteria.
· Unilateral nuclear cat and OAG.
· Diffuse iris atrophy and
white coloration of the
pupillary border (eroded
pupillary border) .
· Hyphema during cataract
· TTT : glaucoma no
steroids
· Diffuse stellate KPs : DD Herpes
Iris atrophy lead to prominent sphiecter pupillae and vessels
· Fine vessels (arrows) are seen crossing the trabecular meshwork. This neovascularization is
not accompanied by a fibrovascular membrane and does not result in peripheral anterior
synechiae formation and secondary angle closure
HS iritis
TTT
· Control IOP
· Oral antiviral : Acyclovir 400 tab x5
for 1-2 weeks ,, Monitor kidney f.
· Predforte : taper over 2 months
· Atropine
JUVENILE IDIOPATHIC
ARTHRITIS
JIA
· Chronic
· Bilateral
· Anterior
· White and quiet
· ANA +ve ,,, -ve RF
· Female < 7ys
· Screening / 2 months
Systemic mainfestations of JIA
1. Stills disease : lymphademopathy ,
splenomegally , rash, uvitis rare : no
follow up.
2. Polyarticular : uvitis uncommon ,,
comes more as acute ,, RF +ve :
follow up every 6 months.
3. Pauciarticular : ANA +ve, RF –ve ,
female , 5-7 years, uvitis common
TTT
· Steroids / cycloplegics
· Methotrexate
· Biologic agents
· Monitoring (75% severe resistant
uvitis )
DD
· Masquarade = retinoblastoma
· Intermediate uvitis = 20% of pediatric uviteitis
· Juvenile HLAB27
· Sarcoidosis
· Others : TB , lyme , $ , toxoplasma
4) GRANULOMATOUS
ANTERIOR UVEITIS
· 1st exclude Medical or surgical (lens induced uveitis /
UGH / endophthalmitis/ fungal infection/ Drugs)
· 2nd exclude herpetic keratouveitis :
corneal affection + iris atrophy or ARN
· 3rd search for specific infections and non infections 
(14) : TB , Toxoplasma, syphilis , Sarcoidosis , lyme ,
lymphoma, leukemia, Endogenous endophthamitis, HSV,
HIV, HCV, , VKH , SO, Multifocal choriditis
ARN
Sarcoidosis
· Bilateral granulomatous
anterior uveitis √√
· Heer fordt ’s syndrome
(uveo-parotid fever):
anterior uveitis, parotid
gland enlargement , facial
palsy, and fever
· ACE (75% of cases) +
hypercalcemia, +ve galium scan
Ocular findings
 Lacrimal gland +++ / NLDO
 Conjunctival nodules, calcifications , symblepharon , calcific band
keratopathy, IK, anterior scleritis.
 Anterior granulomatous uveitis (bilateral granulomatous anterior
uveitis = sarcoidosis UPO)
 Intermediate uveitis
 Retina and choroid nodules , Non occlusive peribhlepitis, candle wax
appearance.
 Sarcoid granuloma of the optic disc / optic neuritis.
 Neurosarcoidosis can also manifest as papilledema, nystagmus, and
visual field defects
TTT
· Systemic steroids
· IMT
· Biologic agents
· Topical cyclosporine for conjunctival
lesions and dry eye.
5) BEHCET’S DISEASE
· Excess cells no flare (iris is seen well)
less pain less injection ,, posterior
synechia with back of the iris
Behcet’s disease
· Recurrent oral ulcer + 2 of four :
· Genital ulcer
· Skin lesions
· Uvitis
· Pethergy test
· Hypopyon is not common 25% - short living
– no fibrin
· bilateral ( > 70%). Posterior/ panuveitis
is the most common form
· HLA-B 51
· Ocular signs : explosive anterior uveitis
Vitritis, necrotizing retinitis, retinal
vasculitis, retinal hemorrhages, retinal
edema, vitreous hemorrhage, capillary
dropout , retinal neovascularization,
TUBULOINTERSTITIAL
NEPHRITIS
· acute, bilateral (DD : behcet ,
psoraisis HLAB27) anterior uveitis
with fever, fatigue, and malaise. It
occurs more often in children < 20
· Generally, the uveitis occurs up o 1
year prior to onset of renal symptoms
· Autoantibodies formation in response to certain antibiotics
or NSAID administration is the presumed eitiology.
Diagnosis by tubulointerstitial infiltration and necrosis with
preserved glomeruli and CD4 lymphocytic infiltration
· TTT : predinsolone 1mg/kg/d
Post streptococcal uveitis
· unilateral or bilateral uveitis with positive anti-streptolysin
O titres (ASOT) or anti-deoxyribonuclease (anti-DNase)
titres, throat culture and negative routine investigations for
other causes of uveitis.
· Age < 16 ys
· Mostly 2 weeks after pharyngitis
· Anterior uveitis / intermediate / sclerokeratitis/
papillophlepitis
· TTT as JIA
Anterior uveitis in elderly
· DM
· HZO / other infections
· Cancer ( Breast / Meningioma)
· O ischemic $
· lymphoma
· Secularism and liberalism do not give us the
answer: Why are we here? Who created the
universe ? What should we do in our life?
Where will we go after life? But it only gives
us false slogans about freedom, conscience,
humanity and rationality, the face of which is
compassion and its interior is the impulse
behind animal instincts, lusts and desires.
INTERMEDIATE UVEITIS
Inflammation localized to the vitreous and
peripheral retina.
Patient
· Young adult and children (20% of
pediatric uveitis)
· Bilateral but assymetric > 80% : dilate
both eyes
· 75% will have BCVA > 0.5 after 5 yrs
symptoms
· Floaters √√
· Blurred vision
signs
· Anterior segment : low grade cells, Kps
· Vitreous cells (lymphocytes)
· Snowballs : aggregates of cells
· vasculitis of peripheral veins / occlusive
· NVE lead to vit.Hge more in children
· Exaudates on the parsplana then collagen
production lead to snowbank = chronic
· ONH edema / optic neuritis
· Yellow white masses at inferior retina
causes
· Idiopathic pars planitis >70%
· MS : anterior uveitis,, posterior synechia,,
vasculitis,, less macular edema,, optic neuritis.
MS can appear years after uvitis
· Sarcoidosis : band keratopathy, symblepharon
and conj deposits, black race, choroidal lesion,
Ex RD
· Others : Lyme/IBD/$/TB/ whipple
DD
· ALL Uveitis
· Lymphoma
· Anteror Uvitis spill or treated or
Fuch’s
· Endogenous endophth
· TB / Toxoplasma
Lab
· CBC/ VDRL and FTA – ABS
· Old age , suspected lymphoma : MRI // CSF
cytology or diagnostic Vx
· Tropical area : Borreilla borgdorfi antibodies
· Sarcoidosis : CXR // serum ACE , Ca++
· MS : Enhanced MRI
· Toxocara ab
· PPD
Imaging
· FA
· OCT
· US
· UBM
· MRI / CXR
Vision loss
· CME √√
· RD exaudative / T- rhegmatogenous may be
chronic / NV and traction can produce huge
break or total RD 360
· Vit hge
· ERM
· CNV
· Glaucoma
· Cataract
· Band k
· Cyclitic membrane and atrophia
clinical
TTT
· Topical steroids : for anterior segment affection
· Periocular TAAC (2-3 injections) for unilateral
cases
· Systemic steroids : for bilateral or cases not
respond to periocular after exx of TB
· Intravitreal TAAC for CME ,, intravitreal
Fluocinolone implant for resistant cases
· Systemic immune suppressive : for resistant
cases and as steroid sparing :
cyclosporine/azathioprine
Biologic agents
· Adalimumab ; for pediatric use and
steroid resistant cases
· Infliximab (antiTNF)
· Interferon B for MS
· Cryo in patients with NVE and
recurrent vit Hge
· Argon laser is alternative
· PP Vx for steroid responders, resistant
CME and retinal traction
· Cataract surgery after patient is cell
free for 3-6 months and IOL is
controversery
· Whoever thinks he has possessed himself by emancipation
from religion is mistaken. A person did not come to the world
with his freedom, and he did not choose his parents, and he
would not leave it with his freedom, and he could not protect
his body from diseases or his immune system from attacking
his eye or control his heartbeat or intestinal movements, so
how can a person possess himself? He only had to answer an
exam that he did not enter voluntarily, and he would not leave
it willingly, and he could not change the questions. Only the
secular person can choose the wrong answer and think that he
owned himself and his freedom ..
Simple uveitis 1

Simple uveitis 1

  • 1.
    Simple Uveitis · MohamedZaky Elkadim · Tanta University
  • 2.
  • 3.
    ANTERIOR UVEITIS 1) Retrocorneal granuloma 2) Acute severe with fibrinous reaction and pain (angry eye) 3) Uveitic glaucoma / White and quiet 4) Granulomatous anterior uveitis 5) Behcet’s disease
  • 4.
  • 6.
    Trematode · History ofcanal water contact · Topical and systemic steroids · TB should be excluded 1st · Surgical excision of granuloma rarely used. · ± shistofast · ± Verm-1 tab 1 tab / week *2 · ± Ca++
  • 7.
    2) ACUTE SEVEREWITH FIBRINOUS REACTION AND PAIN (ANGRY EYE)
  • 9.
    HLA B27 · Themost common anterior uveitis 50% · May be associated with “seronegative spondylo arthropathies”: Reiter, Ankylosing spondylitis, psoraisis, IBD. · Not common in non whites · Severe pain , injection , fibrinous reaction , posterior synechiae · Bacteria such as C hlamydia, Salmonella, Yersinia, and Shigella have been associated.
  • 10.
    If indicated: · MRI : sacroiliac join and lumbar spine · Swab or chlamydia, Shigella, Yersinia, · No KPs : just dusting · Pain on accomodation (pain may precede the attack). · Usually bilateral assymmetric and recur
  • 11.
    causes 1. Idiopathic (1%of HLAB27 will have uveitis). 2. Ankylosing spondylitis : MRI back : most common cause of AAU in male. 3. IBD : investigate for Calprotectin Sulfasalazine 4. Reiter : Azithromycin single dose ,, urine and conj swab ( Urethritis → conjunctivitis→ arthritis → uveitis) 5. Psoraisis → 20% arthritis → 20% AAU ,, bilateral simultaneous 6. Bacterial infection trigger
  • 12.
    3) UVEITIC GLAUCOMA/ WHITE AND QUIET
  • 13.
  • 15.
    POSNER-SCHLOSSMAN SYNDROME (glaucmato cycliticcrisis) · Male ,, unilateral uveitic glaucoma · CMV · Central white KPs with variable size · No synechie no vitritis no heterochromia · Between attacks : only optic cup
  • 17.
    FUCHS’ IRIDOCYCLITIS · Floatersare he main complain · Rubella · FUS is a chronic, anterior, granulomatous with vitreous involvement . · unilateral (90% of cases) · ciliary injection and posterior synechiae are never present and should be viewed as exclusion criteria. · Unilateral nuclear cat and OAG.
  • 18.
    · Diffuse irisatrophy and white coloration of the pupillary border (eroded pupillary border) . · Hyphema during cataract · TTT : glaucoma no steroids
  • 19.
    · Diffuse stellateKPs : DD Herpes
  • 20.
    Iris atrophy leadto prominent sphiecter pupillae and vessels
  • 22.
    · Fine vessels(arrows) are seen crossing the trabecular meshwork. This neovascularization is not accompanied by a fibrovascular membrane and does not result in peripheral anterior synechiae formation and secondary angle closure
  • 23.
  • 26.
    TTT · Control IOP ·Oral antiviral : Acyclovir 400 tab x5 for 1-2 weeks ,, Monitor kidney f. · Predforte : taper over 2 months · Atropine
  • 27.
  • 28.
    JIA · Chronic · Bilateral ·Anterior · White and quiet · ANA +ve ,,, -ve RF · Female < 7ys · Screening / 2 months
  • 30.
    Systemic mainfestations ofJIA 1. Stills disease : lymphademopathy , splenomegally , rash, uvitis rare : no follow up. 2. Polyarticular : uvitis uncommon ,, comes more as acute ,, RF +ve : follow up every 6 months. 3. Pauciarticular : ANA +ve, RF –ve , female , 5-7 years, uvitis common
  • 31.
    TTT · Steroids /cycloplegics · Methotrexate · Biologic agents · Monitoring (75% severe resistant uvitis )
  • 32.
    DD · Masquarade =retinoblastoma · Intermediate uvitis = 20% of pediatric uviteitis · Juvenile HLAB27 · Sarcoidosis · Others : TB , lyme , $ , toxoplasma
  • 33.
  • 36.
    · 1st excludeMedical or surgical (lens induced uveitis / UGH / endophthalmitis/ fungal infection/ Drugs) · 2nd exclude herpetic keratouveitis : corneal affection + iris atrophy or ARN · 3rd search for specific infections and non infections  (14) : TB , Toxoplasma, syphilis , Sarcoidosis , lyme , lymphoma, leukemia, Endogenous endophthamitis, HSV, HIV, HCV, , VKH , SO, Multifocal choriditis
  • 37.
  • 38.
    Sarcoidosis · Bilateral granulomatous anterioruveitis √√ · Heer fordt ’s syndrome (uveo-parotid fever): anterior uveitis, parotid gland enlargement , facial palsy, and fever · ACE (75% of cases) + hypercalcemia, +ve galium scan
  • 39.
    Ocular findings  Lacrimalgland +++ / NLDO  Conjunctival nodules, calcifications , symblepharon , calcific band keratopathy, IK, anterior scleritis.  Anterior granulomatous uveitis (bilateral granulomatous anterior uveitis = sarcoidosis UPO)  Intermediate uveitis  Retina and choroid nodules , Non occlusive peribhlepitis, candle wax appearance.  Sarcoid granuloma of the optic disc / optic neuritis.  Neurosarcoidosis can also manifest as papilledema, nystagmus, and visual field defects
  • 40.
    TTT · Systemic steroids ·IMT · Biologic agents · Topical cyclosporine for conjunctival lesions and dry eye.
  • 41.
  • 42.
    · Excess cellsno flare (iris is seen well) less pain less injection ,, posterior synechia with back of the iris
  • 43.
    Behcet’s disease · Recurrentoral ulcer + 2 of four : · Genital ulcer · Skin lesions · Uvitis · Pethergy test · Hypopyon is not common 25% - short living – no fibrin
  • 45.
    · bilateral (> 70%). Posterior/ panuveitis is the most common form · HLA-B 51 · Ocular signs : explosive anterior uveitis Vitritis, necrotizing retinitis, retinal vasculitis, retinal hemorrhages, retinal edema, vitreous hemorrhage, capillary dropout , retinal neovascularization,
  • 48.
    TUBULOINTERSTITIAL NEPHRITIS · acute, bilateral(DD : behcet , psoraisis HLAB27) anterior uveitis with fever, fatigue, and malaise. It occurs more often in children < 20 · Generally, the uveitis occurs up o 1 year prior to onset of renal symptoms
  • 49.
    · Autoantibodies formationin response to certain antibiotics or NSAID administration is the presumed eitiology. Diagnosis by tubulointerstitial infiltration and necrosis with preserved glomeruli and CD4 lymphocytic infiltration
  • 51.
    · TTT :predinsolone 1mg/kg/d
  • 52.
    Post streptococcal uveitis ·unilateral or bilateral uveitis with positive anti-streptolysin O titres (ASOT) or anti-deoxyribonuclease (anti-DNase) titres, throat culture and negative routine investigations for other causes of uveitis. · Age < 16 ys · Mostly 2 weeks after pharyngitis · Anterior uveitis / intermediate / sclerokeratitis/ papillophlepitis · TTT as JIA
  • 53.
    Anterior uveitis inelderly · DM · HZO / other infections · Cancer ( Breast / Meningioma) · O ischemic $ · lymphoma
  • 58.
    · Secularism andliberalism do not give us the answer: Why are we here? Who created the universe ? What should we do in our life? Where will we go after life? But it only gives us false slogans about freedom, conscience, humanity and rationality, the face of which is compassion and its interior is the impulse behind animal instincts, lusts and desires.
  • 59.
    INTERMEDIATE UVEITIS Inflammation localizedto the vitreous and peripheral retina.
  • 60.
    Patient · Young adultand children (20% of pediatric uveitis) · Bilateral but assymetric > 80% : dilate both eyes · 75% will have BCVA > 0.5 after 5 yrs
  • 61.
  • 62.
    signs · Anterior segment: low grade cells, Kps · Vitreous cells (lymphocytes) · Snowballs : aggregates of cells · vasculitis of peripheral veins / occlusive · NVE lead to vit.Hge more in children · Exaudates on the parsplana then collagen production lead to snowbank = chronic · ONH edema / optic neuritis
  • 63.
    · Yellow whitemasses at inferior retina
  • 64.
    causes · Idiopathic parsplanitis >70% · MS : anterior uveitis,, posterior synechia,, vasculitis,, less macular edema,, optic neuritis. MS can appear years after uvitis · Sarcoidosis : band keratopathy, symblepharon and conj deposits, black race, choroidal lesion, Ex RD · Others : Lyme/IBD/$/TB/ whipple
  • 65.
    DD · ALL Uveitis ·Lymphoma · Anteror Uvitis spill or treated or Fuch’s · Endogenous endophth · TB / Toxoplasma
  • 66.
    Lab · CBC/ VDRLand FTA – ABS · Old age , suspected lymphoma : MRI // CSF cytology or diagnostic Vx · Tropical area : Borreilla borgdorfi antibodies · Sarcoidosis : CXR // serum ACE , Ca++ · MS : Enhanced MRI · Toxocara ab · PPD
  • 67.
    Imaging · FA · OCT ·US · UBM · MRI / CXR
  • 68.
    Vision loss · CME√√ · RD exaudative / T- rhegmatogenous may be chronic / NV and traction can produce huge break or total RD 360 · Vit hge · ERM · CNV · Glaucoma · Cataract · Band k · Cyclitic membrane and atrophia
  • 69.
  • 71.
    TTT · Topical steroids: for anterior segment affection · Periocular TAAC (2-3 injections) for unilateral cases · Systemic steroids : for bilateral or cases not respond to periocular after exx of TB · Intravitreal TAAC for CME ,, intravitreal Fluocinolone implant for resistant cases · Systemic immune suppressive : for resistant cases and as steroid sparing : cyclosporine/azathioprine
  • 72.
    Biologic agents · Adalimumab; for pediatric use and steroid resistant cases · Infliximab (antiTNF) · Interferon B for MS
  • 73.
    · Cryo inpatients with NVE and recurrent vit Hge · Argon laser is alternative · PP Vx for steroid responders, resistant CME and retinal traction · Cataract surgery after patient is cell free for 3-6 months and IOL is controversery
  • 74.
    · Whoever thinkshe has possessed himself by emancipation from religion is mistaken. A person did not come to the world with his freedom, and he did not choose his parents, and he would not leave it with his freedom, and he could not protect his body from diseases or his immune system from attacking his eye or control his heartbeat or intestinal movements, so how can a person possess himself? He only had to answer an exam that he did not enter voluntarily, and he would not leave it willingly, and he could not change the questions. Only the secular person can choose the wrong answer and think that he owned himself and his freedom ..