A Flashcards

1
Q

Retinal astrocytic hamartoma / Retinal astrocytoma - in which diseases

A

Tuberous sclerosis (Bourneville disease), NF1, retinitis pigmentosa

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2
Q

Tuberous sclerosis (Bourneville disease)

A

60% sporadic, triad-epilepsy,mr,adenoma sebaceum, Ash leaf spots, Shagreen patches, skin tags, cafe-au-lait, subependymal astrocytic, giant cell astro., renal angiomyolipoma, cardiac rhabdomyoma, pulmonary lymphangioma, patchy iris hypopigmentation, atypical iris colobomas

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3
Q

Acquired retinal astrocytoma

A

old, solitary, growth, sRD, lipid exudation

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4
Q

Capillary hemangioma (hemangioblastoma)

A

VHL, capillary-like channels, foamy stromal cells, growth, exudation (+remote) , young, anterior

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5
Q

VHL

A

80%AD, Capillary hemangioma, CNS hemangioma, pheochromocytoma, renal pancreatic carcinoma, cysts

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6
Q

Vasoproliferative tumor

A

ant to equator, inferotemp, exu, hemor, sRD, secondary-int uveitis, trauma, pigmentosa, chronic RD,

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7
Q

Cavernous hemangioma

A

sporadic, Oculoneurocutaneus syndrome (AD, CNS cutaneus angiomas), no exud, grapes, FA sedimentation, no photocoagulation

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8
Q

Racemose hemangioma

A

uni, asymptomatic, Wyburn-Mason syndrome (non-hereditary, cutaneous CNS hemangioma)

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9
Q

Combined hamartoma of Retina and RPE

A

uni, associations: none, NF2, Gorlin, brachio-oculofacial s., incontinentia pigmenti, x-linked retinoschisis

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10
Q

Adenoma of RPE

A

vitreous inflammatory cells, exud, feeding artery and vein

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11
Q

Atypical congenital hypertrophy of the RPE

A

Familial adenomatous polyposis, Gardner syndrome (FAP, osteoma skull mandible and long bones, epidermoid cysts, lipomas, fibromas), Turcot s. (AD or AR, FAP, medulloblastoma, glioma)

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12
Q

Melanocytoma - cells

A

large polyhedral or spindle cells

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13
Q

Touton giant cells and large foamy histiocytes

A

Juvenile Xanthogranuloma

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14
Q

Melanoma mnemonic

A

Thickness greater than 2mm, Fluid, Symptoms, Orange , Margin within 3 mm, Ultrasonographic Hollowness, Halo absent, Drusen absent

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15
Q

Which gene mutation is associated with best prognosis in uveal melanoma

A

EIF1AX, SF3B1

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16
Q

Which gene mutation is associated with META in uveal melanoma

A

class 2 gene expression profile (GEP), BAP1

17
Q

What procedure is contraindicated in uveal melanoma

A

diathermy

18
Q

Most common intraocular tumor overall

A

metastases

19
Q

CAR - antibodies

A

anti-recoverin antibodies

20
Q

Type of non-Langerhans’ cell histiocytosis

A

Juvenile Xanthogranuloma