ocular disease lecture

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7/28/2019 ocular disease lecture http://slidepdf.com/reader/full/ocular-disease-lecture 1/67  DISORDERS OF THE EYELIDS 2 Dr Russell J Watkins

Transcript of ocular disease lecture

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DISORDERS OF THEEYELIDS 2

Dr Russell J Watkins

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Entropion

Types

Involutional

Cicatricial

Acute spastic

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Involutional Entropion

Affects lower lid

Possible pathological mechanisms are:

Preseptal portion overrides pretarsal portionof orbicularis oculi

Horizontal lid laxity due to stretched canthaltendons, orbital fat atrophy

Weakened tarsus allowing flexure Vertical instability due to dehiscence of 

retractors

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Involutional Entropion

Treatment of involutional entropion

Taping

Botulinum toxin if unfit for surgery

Surgery

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Cicatricial Entropion

Affects upper or lower lid

Scarring shortens posterior lamella

Causes include trachoma, radiation, chemicalinjury, topical rx, previous surgery, trauma, SJS& mucous membrane pemphigoid

Treatment is usually surgical

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Acute Spastic Entropion

Orbicularis oculi spasm due to ocular irritation oressential blepharospasm

Usually associated with involutional entropion

Management is by removal of irritant, treatmentof associated involutional entropion, botulinumtoxin

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Ectropion

Types of ectropion

Involutional

Cictatricial

Paralytic

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Involutional Ectropion

Usually lower lid

Tarsal stretching ± orbicularis weakness

Treatment is by cicatrising cautery or surgery

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Cicatricial Ectropion

Upper or lower lid

Causes include trauma [lacerations, burns,surgery], tumours, infections

Optometric management - refer

Pay attention to prevention of exposurekeratopathy

Surgical management aimed at release of scarring including skin grafts

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Paralytic Ectropion

Lower lid ±lagophthalmos

Causes: myopathy; CN VII disorders

Optometric management – refer

Pay attention to prevention of exposurekeratopathy

Botulinum toxin induced ptosis; tarsorrhaphy

Various other surgical techniques including nervetransposition

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Blepharospasm

Involuntary tonic, spasmodic, bilateral eyelidclosure

F>M

More common in older individuals (60+ yrs)

Causes - idiopathic, Parkinson’s disease,psychogenic, post-encephalitic, tetany, drugse.g. psychotropics

Treatment - botulinum toxin injections intoorbicularis oculi

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Floppy Lid Syndrome

Generalised laxity of eyelid tissues

Can be unilateral or bilateral

Symptoms - ocular irritation, redness

Signs - SPK, easy distraction of lid from globe,easy upper lid eversion, lower lid ectropion,ptosis

Treatment - wedge excision, canthal tendonrepair

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Orbicularis Myokymia

Involuntary contraction producing an annoyingtwitching sensation

Related to fatigue - a very common presentation

in optometric practice Rarely due to a sinister cause

Hemifacial spasm

Multiple sclerosis

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Benign Eyelid Tumours

Xanthelasma

Fatty plaques (foam cells in epidermis),usually medial, usually bilateral

Associated with 1° hyperlipidaemic states,DM, hypothyroidism, primary biliary cirrhosis

Optometric management - refer to GP forexclusion of underlying cause

Surgical management - excision (60% recur),laser ablation, chemical cautery

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Benign Eyelid Tumours

Basal cell papilloma

Also known as seborrhoeic keratosis

Common

Sessile

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Benign Eyelid Tumours

Squamous cell papilloma

Common

Sessile or pedunculated

Histopathology - excessive convolutedepithelium with central fibrovascular core;may form keratin horn

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Benign Eyelid Tumours

Solar keratosis

Flat, multiple, scaly lesions

Occasionally papillomatous with keratin hornformation

NB: premalignant

Histopathology - epithelial dysplasia withkeratosis BUT no invasion

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Benign Eyelid Tumours

Keratoacanthoma

Rapidly enlarges (months), then regresses

Volcano shaped with keratin plug

Visually, often difficult to distinguish fromBCC, whereas:

Histopathology - difficult to differentiate fromSCC unless whole lesion examined; noinvasion, but basal inflammation

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Benign Eyelid Tumours

Haemangioma

Strawberry naevus: evident in neonatal period

Grows then usually regresses by 5yrs

May be cutaneous, orbital or mixed

Histopathology - capillary proliferation, someof which are uncanalised

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Benign Eyelid Tumours

Neurofibroma

Associated with neurofibromatosis

Histopathology - Schwann cell & fibroblastproliferation

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Benign Eyelid Tumours

Naevi

Congenital collections of naevus cells

Pigmented or non-pigmented

May become pigmented post-puberty

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Benign Eyelid Tumours

Naevi are classified according to location

Epidermal - slightly thickened epithelium withnaevus cells forming cysts

Junctional - activity at epidermal/dermal junction, occuring at puberty

Dermal - collections of naevus cells within thedermis; Can be associated with choroidal

melanomas Compound - malignant

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Benign Eyelid Tumours

Cyst of Moll

Retention cyst

Clear & fluid filled

Cyst of Zeis

Retention cyst

White cheesy (sebaceous) material

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Miscellaneous BenignLumps

Milia

Cutaneous horn

Meibomian cyst

Naevus flammeus

Dermoid cyst

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Malignant Eyelid Tumours

Basal cell carcinoma

Most common malignant carcinoma

Lower lid most common site

Do NOT metastasise but invade locally Types

• Noduloulcerative - well defined; Ulcerated & inflamed lesion

• Sclerosing (morphoea) - tends to be multifocal

Optometric management - refer for cryo, RT or surgery

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Malignant Eyelid Tumours

Carcinoma in situ (Bowen’s disease)

5% of eyelid tumours

Upper lid most common site

Histopathology - dedifferentiation of epithelialcells; localised to epidermis; premalignant forSCC

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Malignant Eyelid Tumours

Squamous cell carcinoma

Arise de novo from premalignant states suchas solar keratoses & xeroderma pigmentosum

Lymphatogenous spread May evoke inflammatory response

Histopathology can be from well differentiatedto anaplastic

Optometric management - refer (radicalexcision)

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Malignant Eyelid Tumours

Malignant melanoma

Very rare (of the eyelid)

Can arise de novo or as a malignant

transformation of a junctional naevus Signs include itching, bleeding, pigmentary

changes, increase in size

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Malignant Eyelid Tumours

Types of malignant melanoma

Lentigo maligna - superficial, premalignant(seen in the elderly)

Superficial spreading melanoma Nodular - occurs only on covered areas not on

face

Optometric management - refer

Prognosis depends on site, depth of invasion(poor if >1.5mm) & degree of inflammation

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Malignant Eyelid Tumours

Meibomian gland carcinoma

Rare

Localised

May present as recurrent chalazion

Optometric management - refer (radicalexcision & RT)

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Miscellaneous Malignant

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Miscellaneous MalignantLumps

Metastatic deposit

Lymphomatous infiltrate

Sebaceous gland carcinoma

Kaposi sarcoma

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