Also called Disc oedema
Passive disc swelling associated with increased intra cranial pressure
Bilateral and asymmetrical
Inflammations such as papillitis, neuroretinitis, papillophlebitis and uveitis.
Ocular hypotony
CRVO, AION (anterior ischemic optic neuropathy) and uremia
Orbital causes – tumors, grave’s orbitopathy and orbital cellulitis
Leukemia and lymphomas
2. INTRODUCTION
•Also called Disc oedema
•Passive disc swelling associated with increased intra cranial pressure
•Bilateral and asymmetrical
3. CAUSES
•Inflammations such as papillitis, neuroretinitis, papillophlebitis and
uveitis.
•Ocular hypotony
•CRVO, AION (anterior ischemic optic neuropathy) and uremia
•Orbital causes – tumors, grave’s orbitopathy and orbital cellulitis
•Leukemia and lymphomas
4. ETIOPATHOGENESIS
•Congenital conditions – aqueductal stenosis, and craniosynostosis
•Intracranial space occupying lesions – brain tumors, tuberculoma,
subdural haematoma, and aneurysms
•ICSOLs of cerebellum, mid brain and parieto occipital region produce
papilloedema
•Intracranial infections – meningitis, encephalitis
•Intracranial hemorrhages
•Obstruction of CSF
•Tumors of spinal cord
6. UNILATERAL VS BILATERAL
•Unilateral – disc swelling due to ocular and orbital lesions
•Bilateral – raised intracranial pressure papilloedema
•Foster Kennedy syndrome – olfactory or sphenoidal meningiomata
and frontal lobe tumors
•Pseudo Foster Kennedy syndrome – unilateral papilloedema
raised intracranial pressure and a pre existing optic atrophy
7. FOSTER KENNEDY SYNDROME
Foster Kennedy syndrome: papilledema in one eye with optic atrophy in
the other eye
Funduscopy in a 36-year-old man with headaches and loss of vision. (A)
Edema of the optic disk (arrows) in the chronic phase (“champagne cork”)
is visible in the right fundus, with venous tortuosity and dilatation
(arrowheads). (B) Left funduscopy shows a pale optic disk, consistent with
axonal death. The lack of colour is more marked in the temporal area
8. PSEUDO FOSTER KENNEDY
SYNDROME
Fundus photograph showing right eye papilledema and left eye optic disc pallor.
Pseudo-Foster Kennedy syndrome in a young woman with meningioma infiltrating the
superior sagittal sinus
10. CLINICAL FEATURES
General features – headache, nausea, projectile vomiting and
diplopia
Ocular features – VA and pupillary reactions usually remains fairly
normal until the late stage of the disease
11. STAGES OF PAPILLOEDEMA –
EARLY (INCIPIENT)
VA and pupillary reactions usually remains normal
Ophthalmic feature – obscuration of the disc
Blurring of peripapillary nerve fibre layer
Absence of venous pulsation
Mild hyperaemia of the disc
Splinter hemorrhages
12.
13. FULLY DEVELOPED PAPILLOEDEMA
Transient visual obscuration in one or both eyes and pupillary
reactions are normal
Optic disc oedema – forward elevation
Cup of the disc is obliterated
Disc becomes hyperaemic and blurring of the margin is present
Multiple cotton wool spots
Veins becomes tortuous and engorged
Paton’s line
Enlargement of the blind spot
14.
15. CHRONIC PAPILLOEDEMA
VA is reduced and pupillary reactions are normal
Acute hemorrhages and cotton wool spots
Optic disc gives the appearance of the champagne cork
Blind spot enlarges and visual field begins to constrict
16.
17. ATROPHIC PAPILLOEDEMA
Develops after 6-9 months
Severely impaired VA
Light reflex is impaired
Greyish white discoloration and pallor disc
Prominence of the disc decreases
Retinal arterioles becomes narrowed and vein become less
congested
White sheathing develops
Concentric contraction of the visual field
20. TREATMENT AND PROGNOSIS
Neurological emergency
CT scan and MRI
Unless the causative disease is treated or cerebral decompensation
is done, the course of papilloedema is chronic and prognosis is bad