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LEUKOCORIA
By: Qurat-ul-ain
Ophthalmic Medical
Technologist/ MBA Health &
Hospital management
Retinoblastoma
• A malignant tumor of the retina that
appears as a white, nodular mass that
breaks through the internal limiting
membrane into the vitreous as a yellowish
sub-retinal mass lesion after underlying a
serous retinal detachment or as a lesion
simulating uveitis.
• Iris neovascularization is common.
• Cataract is uncommon and the eye is
normal in size
Toxocaiasis
• A nematode infection may appear as a
localized, white, elevated granuloma in the
retina or as a diffuse endophthalmitis.
• Localized inflammation of ocular structures,
vitreous traction bands, traction retinal
detachment and cataract.
Coats Disease
• A retinal vascular abnormality resulting in
small multifocal out-pouchings of the
retinal vessels.
• May develop secondary to bullous retinal
detachment associated with sub-retinal
fluid.
PHPV
• A developmental ocular abnormality
consisting of varied degree of glial and
vascular proliferation in the vitreous cavity.
• Membrane behind the lens, place inward
traction on the ciliary processes.
• The membrane and lens may rotate
anteriorly, shallowing the anterior chamber
and resulting in secondary glaucoma.
Pediatric cataract
• Opacity of the lens present at birth.
• May be unilateral and bilateral
• May be associated with systemic disorder.
Retinal astrocytoma
• Slightly elevated, yellowish white retinal
mass that may be calcified and is often
associated with tuberous sclerosis and
rarely neurofibromatosis.
• May occur in optic nerve head (giant
drusen)
ROP
• Predominantly occur in pre-mature
children
• Usually the result of a retinal
detachment.
Others
• Retinal detachment, retinochoroidal,
coloboma, familial exudative
vitreoretinopathy, myelinated nerve
fibers, uveitis, toxoplasmosis, trauma,
CMV retinitis, endophthalmitis, retinal
dysplasia, incontinentia pigmenti, norrie
disease, medulloepithelioma.
WORK UP
• History taking
• Complete ocular examination
• B-scan ultrasonography
• Intravenous fluorescein angiogram
• Computed tomographic scan or magnetic resonance imaging (MRI) of the
orbit and brain
• Serum ELISA test for Toxocara
• Systemic evaluation by pediatrician
• Anterior chamber paracentesis
• EUA
TREATMENT:
 RETINOBLASTOMA:
• Chemo-reduction, chemotherapy, cryo-therapy, thermotherapy, laser
photocoagulation, plaque radiotherapy.
 Toxocariasis:
• Steroids, vitrectomy, laser photocoagulation
 Coats disease:
• Cryotherapy, surgery required for retinal detachment, anti-VEGF agents if significant
exudates, sub-retinal or intraretinal fluid is present.
 PFV:
• Cataract and retrolental glial membrane extraction
• Treat amblyopia
 Pediatric cataract:
• Cataract extraction within days to weeks of discovery, treat amblyopia.
 Retinal astrocytoma: observation
 ROP:
• Ablation of immature, avascular zones of retina. Laser photocoagulation, use of anti-
VEGF intravitreal.
RESOURCES:
• The wills eye manual , 7th edition
THANK YOU!

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9. Leukocoria.pptx

  • 2. Retinoblastoma • A malignant tumor of the retina that appears as a white, nodular mass that breaks through the internal limiting membrane into the vitreous as a yellowish sub-retinal mass lesion after underlying a serous retinal detachment or as a lesion simulating uveitis. • Iris neovascularization is common. • Cataract is uncommon and the eye is normal in size Toxocaiasis • A nematode infection may appear as a localized, white, elevated granuloma in the retina or as a diffuse endophthalmitis. • Localized inflammation of ocular structures, vitreous traction bands, traction retinal detachment and cataract.
  • 3. Coats Disease • A retinal vascular abnormality resulting in small multifocal out-pouchings of the retinal vessels. • May develop secondary to bullous retinal detachment associated with sub-retinal fluid. PHPV • A developmental ocular abnormality consisting of varied degree of glial and vascular proliferation in the vitreous cavity. • Membrane behind the lens, place inward traction on the ciliary processes. • The membrane and lens may rotate anteriorly, shallowing the anterior chamber and resulting in secondary glaucoma.
  • 4. Pediatric cataract • Opacity of the lens present at birth. • May be unilateral and bilateral • May be associated with systemic disorder. Retinal astrocytoma • Slightly elevated, yellowish white retinal mass that may be calcified and is often associated with tuberous sclerosis and rarely neurofibromatosis. • May occur in optic nerve head (giant drusen)
  • 5. ROP • Predominantly occur in pre-mature children • Usually the result of a retinal detachment. Others • Retinal detachment, retinochoroidal, coloboma, familial exudative vitreoretinopathy, myelinated nerve fibers, uveitis, toxoplasmosis, trauma, CMV retinitis, endophthalmitis, retinal dysplasia, incontinentia pigmenti, norrie disease, medulloepithelioma.
  • 6. WORK UP • History taking • Complete ocular examination • B-scan ultrasonography • Intravenous fluorescein angiogram • Computed tomographic scan or magnetic resonance imaging (MRI) of the orbit and brain • Serum ELISA test for Toxocara • Systemic evaluation by pediatrician • Anterior chamber paracentesis • EUA
  • 7. TREATMENT:  RETINOBLASTOMA: • Chemo-reduction, chemotherapy, cryo-therapy, thermotherapy, laser photocoagulation, plaque radiotherapy.  Toxocariasis: • Steroids, vitrectomy, laser photocoagulation  Coats disease: • Cryotherapy, surgery required for retinal detachment, anti-VEGF agents if significant exudates, sub-retinal or intraretinal fluid is present.
  • 8.  PFV: • Cataract and retrolental glial membrane extraction • Treat amblyopia  Pediatric cataract: • Cataract extraction within days to weeks of discovery, treat amblyopia.  Retinal astrocytoma: observation  ROP: • Ablation of immature, avascular zones of retina. Laser photocoagulation, use of anti- VEGF intravitreal.
  • 9. RESOURCES: • The wills eye manual , 7th edition