intraocular tumours Flashcards

1
Q

Name the uveal melanomas

A
  • Malignant melanoma - choroid
  • Malignant melanoma - CB
  • Malignant melanoma - iris
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2
Q

Discuss the features of a choroidal naevus

A
  • benign melanoma
  • size: 1-2DD, most <5mm, <1mm thick (larger = malignant), stationary in size
  • mx: observe, monitor, review 1-2 yrs
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3
Q

Signs and symptoms of choroidal malignant melanoma

A
  • No symptoms if small, if larger - metamorphopsia, photopsia, VF loss
  • Signs: pigmented lesion (orange tinge, varied colour), irregular, patchy, round, Serous detachment at margins (retinal folds), vascularisation (choroidal BV), haemorrhage, CMO common, vitreous haem, cataract, anterior uveitis (due to tumour necrosis), increase IOP (large –> spread to anterior chamber angle)
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4
Q

Features of choroidal malignant melanoma

A
  • enlargement restricted: sclera and choroid
  • Penetration through BM: “collar button” effect
  • ## Penetration through sclera: extension into orbit
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5
Q

Diagnosis of choroidal naevus vs. melanom

A
TFSOM 
- Thickness (>2mm) 
- Subretinal fluid 
- Symptoms (reduced VA) 
- Orange pigment 
- Melanoma hollow
- Diameter (>5mm)
==> 5 year estimate of progression 
1% (no risk factor), 11% (1 risk factor), 22% (2 factors), 34% (3 risk factors), 51% (4 risk factors), 55% (5 factors)
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6
Q

Managing choroidal malignant melanoma

A
  • Refer
    Fl angio (vascularisation)
  • plaque irradiation (can lead to radiation retinopathy), laser photocoagulation, transpupillary thermography, local resection (enter via sclera, remove tumour), enucleation
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7
Q

Features of CB malignant melanoma

A
  • blurred vision or no symptoms
  • lens anomalies (odd astig, cataract, subluxation)
  • dilated episcleral vessels
  • sub-conj pigment
  • IOP (decrease: less aqu pigment, increase: extension into angle, outflow obstruction)
  • Anterior uveitis (necrosis)
    Mx: refer. Local resectioning (iridocyclectomy), enucleation
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8
Q

Features of iris malignant melanoma

A
  • ‘Brown spot on eye’ , no symptoms
  • Pigmented nodule, angle invasion (+/- glaucoma), cataract, pupil distortion (corectopia), iris neovasc, pigment dispersion
  • MX: refer, surgical excision (iridectomy, iridotrabeculectomy), enucleation
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9
Q

Iris naevus vs. iris melanoma

A

ABCDEF

  • age - young <40 years
  • blood - hyphaema
  • clock hour inferiorly
  • diffuse
  • ectropion
  • feathery margins
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10
Q

Features of retinoblastoma

A
  • Most common tumour of childhood, mostly unilateral, trilateral possible
  • leukocoria, strabismus, uveitis, glaucoma, proptosis, elevated lesion (white, pink)- may grow into vitreous or subretinal space, cause haems, RD
  • MX: examine fundi of children with squint, refer, radiotherapy, photocoagulation/ cryotherapy, enucleation
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11
Q

Features of rhabdomyosarcoma

A

= most common primary orbital tumour of childhood
- risk spread from skull to orbit
- rapid progressive ptosis, squint, gaze restriction
- refer - radiotherapy, chemotherapy
severe cases: exenteration of orbit

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12
Q

Features of Angiomatosis retinae (Von Hippel Lindau disease)

A

= retinal vascular tumour

  • MA –> small red nodule –> large red/orange tumour
  • tortuous vessels, exudate (leaky), vitreous haem, serous RD
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13
Q

Features of primary intraocular lymphoma

A

= tumour of lymphoid tissue/ lymphocytes

  • vitreous cells, multifocal intraretinal or subretinal infiltrates
  • radiotherapy, chemo
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14
Q

Features of choroidal osteoma

A

= benign bone-like choroidal tumour (bony plate in choroid)

  • bony gold/orange plate-like lesion
  • may disrupt RPE and sensory retina - subretinal neovasc
  • mx: benign, may extend under macula (affect vision)
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