2. UVEA – ANATOMY REVIEW
• It is the middle vascular coat of the eye
• It composed of iris, choroid and ciliary body
• It lies between sclera and retina layers of the
eye
• It is the main vascular tissue of the eye
4. IRIS
• It lies most anterior part of uvea
• Made of blood vessels and connective tissues
• Composed of melanocyte and and other
pigmented cells
• Contains central perforation called pupil
• The pupil is made up smooth muscles which
control pupil size ,hence regulate the amont of
light entering the eye
• Dilator papillae(dillate)->sympathetics and
sphincter papillae(constrict)->parasympathetic
6. CILIARY BODY
• Middle part of the uvea
• It’s triangular in shape
• It produce aqueous humor
• Involved in accomodation
• Contained aqueous drainage
8. CHOROIDS
• Posterior part of the uvea
• Nourishes the outer portion of the retina
• Composed of layers of blood vessels
10. DEFINITION
• Uveitis means inflamation of uvea tracts
• It affects adjacent structure like
cornea,vitreous humor,retina and optic nerve
• It causes visual impairment leading to
blindness
11. CLASSIFICATION OF UVEITIS
Many classification of uveitis are used
Anatomical classification
• Anterior uveitis - This involve the iris [Iritis]
ciliary body [cyclitis] or both [iridocyclitis]
• Intermediate uveitis - predominantly involve
the pars plana; subset of this group is called
pars plinitis
12. • Posterior uveitis - inflammation is mainly
behind the base of vitrous, this may be
subdivided into retinochoroiditis and
chorioretinitis depending on the degree of
retina involvement
• Penuveitis - in defuse or penuiveits the entire
uveal tract is involved
13. CLINICAL CLASSIFICATION
• Uveitis may be:
– acute,
– sub acute,
– chronic,
– Recurrent,
– non recurrent
• depending on the speed of onset and
subsequent course
14. AETIOLOGICAL CLASSIFICATION
EXOGENOUS UVEITIS
• This is caused by the trauma or by the
invasion of the eye with the micro organism
from outside
ENDOGENOUS UVEITIS
• This may be caused by direct invasion or
autoimmune reaction to microorganism from
within the patient
15. • -underlying systemic disease including arthritis
(ankylosing spondylitis)
• infection (tuberculosis) and granuloma (sarcoid)
• -parasitic infestation e.g. toxoplasmosis
• -viral infection e.g. cytomegalovirus
• -fungal infection e.g. candidiasis-idiopathic specific
uveitis cases who have unique features of their own
e.g.
• Fuchs heterochromic cyclitis
• -idiopathic non specific uveitis. These cases have no
identified underlying cause and are the majority of
all cases.
16. PATHOLOGICAL CLASSIFICATION
• Uveitis may be classified as:
– granulomatous.,
– non granulomatous
• depending on the appearance of the keratic
precipitates.
• However there is considerable overlap in the
clinical behavior and the etiological
characteristics between of the two groups.
19. AUTOIMMUNE CONDITIONS
• Juvenile Idiopathic Arthritis
o Common in children 5 – 6 years of age
o Common cause of bilateral non granulomatous
iridocyclitis
o Girls are affected four times more than boys
• Ankylosing Spondylitis
o 55% of patients with ankylosing spondylitis develop
anterior uveitis
• Fuch’s Heterochromie Iridocyclitis (Fuch’s Uveitis
Sydrome)
o Uncommon, accounts for <5% causes of all causes of
uveitis.
o Insidious onset during third or fourth decade of life.
20. • Lens – induced uveitis (phacogenic)
o Autoimmune disease directed against the lens antigens
• Others Autoimmune conditions:
o Reiter’s Syndrome
o Ulcerative colitis
o Sarcodosis
o Crohn’s disease
o Psoriasis
MALIGNANT CONDITIONS
o Retinoblastoma
o Leukemia
o Lymphoma
o Malignant melanoma
Traumatic Uveits: includes penetrating injuries and retinal
detachment.
21. CAUSES OF POSTERIOR UVEITIS
• Can be grouped into:
1.Infectious causes and
2.Non infectious causes
• Most causes of posterior uveitis are associated
with some form of systemic disease.
28. DIAGNOSIS OF UVEITIS
• Ocular and general medical history and
examination with particular attention to the skin,
joints and the respiratory system.
• The following tests are frequently helpful:
1. Chest X ray for sarcoid and tuberculosis
2. X ray of the lumbosacral spine and
sacroiliac joints for ankylosing spondylitis
3. Serology for syphilis
4. Full blood count
5. ESR
6. Toxoplasma antibodies
29. SLIT-LAMP EXAM
• A slit-lamp consists of a
microscope and a
powerful beam of light.
• If you have uveitis, you'll
have large number of
white blood cells inside
your eye.
• They will appear as a hazy
fluid/keratic precipitates
(clusters of WBCs) when
studied under the slit-
lamp
30. TREATMENT OF UVEITIS
• Treatment of underlying infection should
relieve the inflammation in your eyes.
• Corticosteroids are the main type of
medication used to treat non-infectious
uveitis which can be in form of eye drops,
injections, oral medication.
• Mydriatics (drugs to dilate pupils)
• Immunosuppressant (only when steroids fails)
• Surgery (during cataract complications)
32. COMPLICATIONS OF UVEITIS
• Fourth leading cause of blindness in the
developed countries
Complications:
1. Cataract
2. Raised eye pressure (Glaucoma)
3. Cystoid macular edema
4. Hypotony
5. Detached Retina
33. CATARACT
• The inflammation inside the eye that's
associated with uveitis can sometimes irritate
the lens of the eye, causing cloudy patches on
the surface of the lens to develop. The cloudy
patches are known as cataracts. They can cause
symptoms such as:
blurred vision
problems seeing clearly at night
colours appearing unusually faint
• Cataracts are usually treated using surgery to
remove the affected lens and replace it with an
artificial one.
35. RAISED EYE PRESSURE (GLAUCOMA)
• Untreated uveitis can cause the iris to stick to the
front surface of the lens. This prevents fluid draining
through the pupil and it increases the pressure inside
the eye.
• The raised pressure inside your eye can damage the
optic nerve and disrupt your normal vision, such as
causing misty vision and rings or halos to appear
around lights. This is known as glaucoma.
• Treatment options for glaucoma include:
• eye drops
• laser treatment
• surgery
37. CYTOID MACULAR EDEMA
• Cystoid macular edema is a complication that can affect
some people with chronic uveitis.
• Prolonged inflammation can result in a build-up of fluid
inside the retina. This can disrupt its ability to function
normally and lead to a painless loss of central vision, i.e.
you'll notice a black spot in your field of vision.
• Cystoid macular oedema can be treated using
corticosteroid eye drops to reduce inflammation inside
the eye and disperse the fluid inside the retina.
• In some cases, a person’s vision will recover once
treatment is initiated. However, this isn't always the case
in severe cases of cystoid macular oedema. Hence the
condition is a leading cause of visual impairment in
people with chronic uveitis.
39. HYPOTONY
• Hypotony is usually defined as an intraocular pressure
(IOP) of 5 mm Hg or less. Low IOP can adversely impact
the eye in many ways, including corneal
decompensation, accelerated cataract formation,
maculopathy, and discomfort. Clinically significant
changes occur more frequently as the IOP approaches 0
mm Hg.
• Inflammation plays a key role in the evolution of
hypotony. It causes increased permeability of the
blood-aqueous barrier and impairs ciliary body aqueous
production
• Hypotony is best managed by correcting the underlying
problem.
40. RETINAL DETACHMENT
• In retinal detachment, the retina pulls away
from the choroid, the layer of blood vessels
that supply the eye with critical oxygen and
nutrients.
• Retinal detachment most often occurs due to
the development of a hole or tear in the
retina. This allows fluid to flow between the
retina and the choroid, resulting in retinal
detachment.
• Retinal detachment will continue to increase
in size if not treated.
P.S. In selected cases, a vitreous biopsy is indicated. Cytology, culture and sensitivity of this biopsy may establish the diagnosis.
Ankylosing spondylitis (AS, from Greek ankylos, stiff; spondylos, vertebrae), previously known as Bekhterev's disease, Bekhterev syndrome, and Marie-Strümpell disease is a chronic inflammatory disease of the axial skeleton with variable involvement of peripheral joints and nonarticular structures. AS is a form of spondyloarthritis, a chronic, inflammatory arthritis and autoimmune disease.[1] It mainly affects joints in the spine and the sacroiliac joint in the pelvis, and can cause eventual fusion of the spine.
It is a member of the group of the spondyloarthropathies with a strong genetic predisposition. Complete fusion results in a complete rigidity of the spine, a condition known as "bamboo spine".[2]
With highest magnification it is sufficient to show the abnormal presence of cells within the aqueous, such as red or white blood cells or pigment granules.
Aqueous turbidity, called "flare," resulting from increased protein concentration can be detected in the presence of intraocular inflammation. Normal aqueous is optically clear, without cells or flare