RETINOBLASTOMA
1. Important facts
2. Presentation
3. Signs
• Endophytic
• Exophytic

4. Treatment
5. Poor prognostic facto...
Important facts
1. Most common primary, malignant, intraocular
tumour of childhood (1:20,000)
2. No sexual predilection
3....
Presentations of retinoblastoma

• Leukocoria - 60%

• Anterior segment invasion

• Strabismus - 20%

• Secondary glaucoma...
Early endophyliticretinoblastoma

White flat lesion

Placoid lesion
More advanced endophytic retinoblastoma

Friable white mass

Cottage cheese appearance

Fine surface blood vessels

Vitreo...
Exophytic retinoblastoma

Multiglobulated white mass with
overlying retinal detachment

May be difficult to visualize
thro...
CT diagnosis of retinoblastoma
Calcification

• Optic nerve involvement
• Orbital and CNS extension
• Pinealoblastoma
Treatment Options of Retinoblastoma
1. Small tumours

Laser photocoagulation
• Transpupillary thermotherapy
• Cryotherapy
...
Poor Prognostic Factors in Retinoblastoma
1. Optic nerve involvement
2. Choroidal invasion
3. Large tumour
4. Anterior loc...
Histology of retinoblastoma

Well-differentiated with many
Flexner-Wintersteiner rosettes

Poorly differentiated
Differential diagnosis of leukocoria
Congenital cataract

Persistent hyperplastic
primary vitreous

Inflammatory cyclitic
...
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Retinoblastoma in short - By :Mayank Kesharwani (KGMU)

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Retinoblastoma in short - By :Mayank Kesharwani (KGMU)

  1. 1. RETINOBLASTOMA 1. Important facts 2. Presentation 3. Signs • Endophytic • Exophytic 4. Treatment 5. Poor prognostic factors 6. Histology 7. Differential diagnosis of leukocoria
  2. 2. Important facts 1. Most common primary, malignant, intraocular tumour of childhood (1:20,000) 2. No sexual predilection 3. Presents before age of 3 years (average 3 months) 4. Heritable (40%) or non-heritable (60%) 5. Predisposing gene (RPE 1) on 13q14
  3. 3. Presentations of retinoblastoma • Leukocoria - 60% • Anterior segment invasion • Strabismus - 20% • Secondary glaucoma • Orbital inflammation • Orbital invasion
  4. 4. Early endophyliticretinoblastoma White flat lesion Placoid lesion
  5. 5. More advanced endophytic retinoblastoma Friable white mass Cottage cheese appearance Fine surface blood vessels Vitreous seedings
  6. 6. Exophytic retinoblastoma Multiglobulated white mass with overlying retinal detachment May be difficult to visualize through deep detachment
  7. 7. CT diagnosis of retinoblastoma Calcification • Optic nerve involvement • Orbital and CNS extension • Pinealoblastoma
  8. 8. Treatment Options of Retinoblastoma 1. Small tumours Laser photocoagulation • Transpupillary thermotherapy • Cryotherapy • 2. Medium tumours Brachytherapy • Chemotherapy • External beam radiotherapy • 3. Large tumours Chemotherapy followed by local treatment • Enucleation • 4. Extraocular extension • External beam radiotherapy 5. Metastatic disease • Chemotherapy
  9. 9. Poor Prognostic Factors in Retinoblastoma 1. Optic nerve involvement 2. Choroidal invasion 3. Large tumour 4. Anterior location 5. Poor cellular differentiation 6. Older children
  10. 10. Histology of retinoblastoma Well-differentiated with many Flexner-Wintersteiner rosettes Poorly differentiated
  11. 11. Differential diagnosis of leukocoria Congenital cataract Persistent hyperplastic primary vitreous Inflammatory cyclitic membrane Unilateral Unilateral or bilateral Coats disease Posterior pole toxocara granuloma Advanced retinopathy of prematurity Unilateral Unilateral Unilateral or bilateral Always bilateral but may be asymmetrical
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