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67 Cards in this Set
- Front
- Back
Foreign body granulomatous reaction to lipid of meibomian glands or Zeis glands
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Chalazion
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What is considered the "foreign body" in Chalazion
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lipid excreted from meibomian/zeis glands
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Chalazion: histology
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granuloma, giant cells, lymphocytes, plamsa cells and PMNS
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waxy, raised nodules with umbilicated center
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Moluscum contagiosum
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soft, yellowish plaques on medial aspect of eyelids
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xanthelasma
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xanthelasma: association
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hyperlipidemia
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xanthelasma: histology
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foamy cells in superficial dermis
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Touton giant cells
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Juvenile xanthogranuloma
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yellow-orange skin nodules in children
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Juvenile xanthogranuloma
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why are the lesions in Juvenile xanthogranuloma yellow
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vascular
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spontaneous, non-traumatic hyphema (blood in anterior chamber) in children
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Juvenile xanthogranuloma
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T/F: most nevi of the eyelids are congenital
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F: most are acquired
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MC malignant tumor of the eyelid
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BCC
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Where does BCC appear with respect to the eyelid
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Lower>medial>upper
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raised, firm nodule with "pearly" borders on upper eyelid
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BCC
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Nodular BCC histology
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nests and cords of proliferating epidermal basal cells
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T/F BCC mets to lung
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false, it is rare for BCC to met
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BCC: tx
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complete resection
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carcinoma that mimics chalazium
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sebaceous carcinoma
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Sebaceous carcinoma: who
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elderly
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Sebaceous carcinoma: where
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meibomian, zeis or glands associated with caruncle
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tumor of zeis glands that grows in nests with central necrosis. May be solid or papillary
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sebaceous carcinoma
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fungating mass on eyelid with keratin on surface
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SCC
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T/F: SCC mets to lymph nodes
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T
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only disease of the conjunctiva
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benign ocular cicatricial pemphigoid
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benign ocular cicatricial pemphigoid: who
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elderly
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adhesions (symblepharon), entropion(eyelid turned inward), trichiasis, corneal scarring
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benign ocular cicatricial pemphigoid
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5 layers of the cornea
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epithelium, bowman's, stroma, descements, endothelium
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embryologic origin of cornea
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neural crest
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cause of corneal edema
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loss of endothelial cells
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The number of endothelial cells in the cornea decreases with …
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age
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who is most suceptible to corneal infection
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those who wear contact lenses and don't use sterile solutions
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inflammation of cornea
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acanthamoeba keratitis
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star-shaped cyst, ring infiltrate, not a lot of inflammatory cells
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acanthamoeba keratitis
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4MC indications for corneal transplant
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aphakic/pseudophakic bullous keratopathy, Fuchs dystrophy, keratoconus and graft failure
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55yo female with cloudy cornea and corneal edema
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fuchs endothelial dystophy
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guttata, thickened Descement's membrane, loss of endothelial cells
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fuchs endothelial dystophy
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Keratoconus may be associated with…
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atopy, Downs, Marfans
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bilateral central ectasia of cornea that produces myopia and irregular astigmatism
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keratoconus
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keratoconus: early histo changes
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breaks in epitheliam BM and Bowmans, central stromal thinning, anterior stromal scarring
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fleisher ring
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keratoconus
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munson's sign
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keratoconus
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Intraocular neuroblastic tumor
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retinoblastoma
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Intraocular melanocytic tumor
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malignant melanoma of the uvea
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MC tumor to eye
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mets (esp to choroid) from BC,lung, leukemia
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MC intraocular malignancy of childhood
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retinoblastoma
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retinoblastoma: uni or bilateral
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33% bilateral
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Leukocoria
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retinoblastoma
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retinoblastoma: gene
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chromosome13 tumor suppressor
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round, oval or spindle-shaped nuclei; hyperchromatic, necrosis, calcification, Flexner-Wintersteiner rosettes
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retinoblastoma
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Homer Wright rosettes
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retinoblastoma, neuroblastoma or medulloblastoma
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what's in the lumen of homer wright rosettes
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eosinophilic cytoplasm
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Most important risk/prognostic factor for retinoblastoma
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extraocular extension
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MC primary intraocular tumor of adults
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malignant melanoma of the uvea
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melanoma of the uvea: who
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53yo blue-eyed Europeans
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melanoma of the uvea: MC location
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choroids
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melanoma of the uvea: clinical presentation
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visual loss, glaucoma, inflammatory signs mimicking endophthalmitis
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melanoma of the uvea: prognostic factors
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size
cell type |
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melanoma of the uvea: cell types
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spindle cell
epithelioid cell mixed cell |
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Do melanomas of the uvea met via lymphatic or hematogenous spread
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hematogenous to liver. the uvea and orbit lack lymphatics.
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MC primary malignant orbital tumor of childhood
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rhabdomyosarcoma
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sudden proptosis in medial, inferior or posterior quadrant
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rhabdomyosarcoma
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rhabdomyosarcoma: 3 histologic growth patterns
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embryonal(most common)
alveolar differentiated |
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spindle cells are arranged ina loose syncytium with occasional cells bearing cross-striations; desmin+
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rhabdomyosarcoma
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rhabdomyosarcoma: 5yr survival
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92%
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Optic nerve atrophy: etiology
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ascending atrophy: loss of retinal ganlion cells b/c of glaucoma/infarction
descending: pathology in cranial cavity or orbit |
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large cystic spaces containing mucopolysaccharide material posterior to lamina cribrosa
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cavernous optic atrophy of schnabel
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