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    By

    Dr. JUSUF FANTONI SpPA,MScPath(Glasg)

    EYE PATHOLOGY

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    EYE PATHOLOGY

    Eyelid

    The eyelid is a composite of skin externally and a mucosa

    (the conjunctiva) on the surface opposed to the eye. Aside from

    protecting the eye, elements within the eyelid generate critical

    components of the tear film. Accessory lacrimal glands, eccrineand apocrine glands populate the eyelid. The sebaceous glands

    ( eis glands associated with the eyelash and the !eibomian

    glands embedded within the eyelid fibrous tarsus ), which helps to

    retard evaporation of tears. "f the drainage system of the sebaceous

    glands is obstructed by chronic inflammation at the eyelid margin

    (blepharitis ), or by neoplasm, then lipid may extravasate into

    surrounding tissue and provoke a granuloamtous response # a lipo$

    %ranuloma, or chalazion.

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    Neoplasm

    The most common malignancy of the eyelid is basal

    cell carcinoma. The second is sebaceous carcinoma, not S

    C C. Surprisingly, primary melanomas of the eyelid skinare extremely rare.

    Eyelid neoplasms may distort tissue and prevent the

    eyelids from closing completely. Exposure of the cornea is

    not only painful, but also might predispose the patient tocorneal ulceration. B C C has a distinct predilection for the

    lower eyelid and medial canthus.

    Sebaceous carcinoma may mimic chalaion or may

    diffusely thicken the eyelid.

    Morphology

    !n moderately differentiated or well"differentiated sebaceous

    carcinoma, vacuoliation of the cytoplasm is present.

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    !t may mimic B C C. #agetoid spread may mimic

    Bowenoid actinic keratosis in the eyelid and carcinoma in situ in the

    con$unctiva. Sebaceous carcinoma may spread through the con$unctival

    epithelium and the epidermis to the lacrima drainage system and the

    nasopharynx

    Cornea

    %nteriorly, the cornea is covered by epithelium that

    rests on a basement membrane. Bowman&s layer, situated$ust beneath the epithelial basement membrane, is

    acellular and forms an efficient barrier against the

    penetration of malignant cells from the epithelium into the

    underlying stroma.The corneal stroma lacks blood vessels and lymphatic

    a featue that contributes to the transparancy of the

    cornea.

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    The corneal endotehlium is derived from neural crest

    and is related to vascular endothelium.

    'eratitis and ulcers(arious pathogens """ bacterial, fungal, viral ) especially

    herpes simplex and herpes oster *, and protooal

    ) %canthamoeba* may cause corneal ulceration.

    !n al forms of keratitis, dissolution of the corneal stromamay be accelerated by activationb of collagenenases within

    corneal epithelium and stromal fibroblasts )+'eratocytes*.

    eoplasms

    The most common intraocular malignancy of adults is

    metastasis to the uvea, typically to the choroid.

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    The appearance of metastases to the eye is sugges"

    tive of extremely short survival, and treatment of occular

    metastases is usually palliative and delivered by radiation

    therapy.

    Ueal Ne! a"# Mela"omas

    -veal melanoma is the most common primary intraocular

    malignancy of adults. !ncidence increases with age. -nlike cutaneous

    melanoma, the occurrence of uveal melanoma has remained stable

    over many years. The etiology of uveal melanoma is unresolved at

    this time.

    There are no lymphatics within the eye, hence, uveal

    melanomas, with very rare exception, spread exclusively by a

    hematogenous route ) the only exception being the rare case of

    melanoma that spreads through the sclera and invades the con$uctiva,

    thereby gaining access to con$unctival klynmphatics *. ost uveal

    mnelanomas spread first to the liver.

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    $et!"a

    /etinal eoplasms

    $et!"o%lastoma

    & the most common primary intraocular malignancy of children.

    The cell of origin of retinoblastoma is neuronal. #rognosis is

    adversely affected by extraocular extension and invasion along the

    optic nerve and possibly by choroidal invasion.

    /etinoblastom occurs in individuals who inherit a germ"line

    mutation of one RB allele. /etinoblastomas arising in the context of

    germ line mutations not only may be bilateral, but also may be

    associated with pinealoblastoma ) so called 0 trilateral retinoblastoma*

    Morphology

    Tumors may contain both undifferentiated and differentiated

    element. The former appear as collections of small, round cells with

    hyperchromatic nuclei.

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    !n well"differentiated tumors there 1lexner"2intersteiner

    rosettes and fleurettes reflecting photoreceptor differentiation. !t should

    be noted, however, that the degree of tumor differentiation does not

    appear to be associated with the prognosis.

    Tumor cells are encircling tumor blood vessels with onesof necrosis typically found in relatively avascular areas. This illustrates

    graphically the dependance of retinoblastom on its blood supply.

    /etinoblastom tends to spread to the brain and bone

    marrow and seldom disseminates to the lungs.

    % benign variant of retinoblastoma " retinocytoma "" has

    been reported. The appearance of retinoblastoma in one eye and

    retinocytoma in the other eye is characteristic of heritableretinoblastoma.