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Transcript of ocular disease lecture
7/28/2019 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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