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==Overview==
==Overview==
==Classification==
==Classification==
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! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|MRI component}}
! style="background: #4479BA; width: 400px;" | {{fontcolor|#FFF|Features}}
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:Group A
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*Retinoblastoma 3 mm or less in basal dimension or thickness, located at least 3 mm from the foveola and 1.5 mm from the optic nerve.
|-
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:Group B
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*Retinoblastoma not in Group A with 1 or more of the following:
**Macular location (≤3 mm to foveola)
**Juxtapapillary location (≤1.5 mm to optic nerve)
**Additional subretinal fluid (≤5 mm from margin).
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
:Group C
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*Retinoblastoma tumor with 1 of the following:
**Focal subretinal seeds
**Focal vitreous seeds
**Both focal subretinal and vitreous seeds.
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
:Group D
| style="padding: 5px 5px; background: #F5F5F5;" |
*Retinoblastoma tumor with 1 of the following:
**Diffuse subretinal seeds
**Diffuse vitreous seeds
**Both diffuse subretinal and vitreous seeds.
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
:Group E
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*Very high-risk eyes with 1 or more of the following:
**Neovascular glaucoma
**Massive intraocular hemorrhage
**Aseptic orbital cellulitis
**Tumor anterior to the vitreous face
**Tumor touching the lens
**Diffuse infiltrating retinoblastoma
**Phthisis bulbi (also known as end-stage eye, this is a nonfunctioning, atrophic, scarred, and disorganized globe, frequently with dystrophic calcification).
|}

Revision as of 17:53, 8 October 2015

Retinoblastoma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]

Overview

Classification

MRI component Features
Group A
  • Retinoblastoma 3 mm or less in basal dimension or thickness, located at least 3 mm from the foveola and 1.5 mm from the optic nerve.
Group B
  • Retinoblastoma not in Group A with 1 or more of the following:
    • Macular location (≤3 mm to foveola)
    • Juxtapapillary location (≤1.5 mm to optic nerve)
    • Additional subretinal fluid (≤5 mm from margin).
Group C
  • Retinoblastoma tumor with 1 of the following:
    • Focal subretinal seeds
    • Focal vitreous seeds
    • Both focal subretinal and vitreous seeds.
Group D
  • Retinoblastoma tumor with 1 of the following:
    • Diffuse subretinal seeds
    • Diffuse vitreous seeds
    • Both diffuse subretinal and vitreous seeds.
Group E
  • Very high-risk eyes with 1 or more of the following:
    • Neovascular glaucoma
    • Massive intraocular hemorrhage
    • Aseptic orbital cellulitis
    • Tumor anterior to the vitreous face
    • Tumor touching the lens
    • Diffuse infiltrating retinoblastoma
    • Phthisis bulbi (also known as end-stage eye, this is a nonfunctioning, atrophic, scarred, and disorganized globe, frequently with dystrophic calcification).