Molluscum contagiosum

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Presentation transcript:

Molluscum contagiosum BENIGN EYELID LESIONS 1. Nodules Chalazion Acute hordeola Molluscum contagiosum Xanthelasma 2. Cysts Cyst of Moll Cyst of Zeiss Sebaceous cyst Hidrocystoma 3. Tumours Viral wart Keratoacanthoma Naevi Capillary haemangioma Port-wine stain Pyogenic granuloma Cutaneous horn

Signs of chalazion (meibomian cyst) Painless, roundish, firm lesion within tarsal plate May rupture through conjunctiva and cause granuloma

Histology of chalazion Epithelioid Multinucleated cells giant cells Multiple, round spaces previously containing fat with surrounding granulomatous inflammation

Treatment of chalazion Injection of local anaesthetic Insertion of clamp Incision and curettage

Acute hordeola Internal hordeolum External hordeolum (stye) ( acute chalazion ) External hordeolum (stye) Staph. abscess of meibomian glands Staph. abscess of lash follicle and associated gland of Zeis or Moll Tender swelling within tarsal plate Tender swelling at lid margin May discharge through skin or conjunctiva May discharge through skin

Molluscum contagiosum Signs Complications Painless, waxy, umbilicated nodule Chronic follicular conjunctivitis May be multiple in AIDS patients Occasionally superficial keratitis

Histology of molluscum contagiosum Lobules of hyperplastic epithelium Intracytoplasmic (Henderson-Patterson) inclusion bodies Circumscribed lesion Surface covered by normal epithelium except in centre Deep within lesion bodies are small and eosinophilic Near surface bodies are larger and basophilic

Xanthelasma Common in elderly or those with hypercholesterolaemia Yellowish, subcutaneous plaques containing cholesterol and lipid Usually bilateral and located medially

Eyelid cysts Eccrine sweat gland hidrocystoma Cyst of Moll Translucent On anterior lid margin Similar to cyst of Moll Not confined to lid margin Cyst of Zeis Sebaceous cyst Opaque On anterior lid margin Cheesy contents Frequently at inner canthus

Viral wart (squamous cell papilloma) Most common benign lid tumour Raspberry-like surface Pedunculated Sessile

Histology of viral wart Finger-like projections of fibrovascular connective tissue Epidermis shows acanthosis (increased thickness) and hyperkeratosis Rete ridges are elongated and bent inwards

Keratoses Seborrhoeic Actinic Common in elderly Affects elderly, fair-skinned individuals Discrete, greasy, brown lesion Most common pre-malignant skin lesion Friable verrucous surface Rare on eyelids Flat ‘stuck-on’ appearance Flat, scaly, hyperkeratotic lesion

Keratoacanthoma Lesion above surface epithelium Uncommon, fast growing nodule Acquires rolled edges and keratin-filled crater Central keratin-filled crater Involutes spontaneously within 1 year Chronic inflammatory cellular infiltration of dermis

Naevi Intradermal Junctional Compound Appearance and classification determined by location within skin Tend to become more pigmented at puberty Intradermal Junctional Compound Elevated Flat, well-circumscribed Has both intradermal and junctional components May be non-pigmented Pigmented No malignant potential Low malignant potential

Capillary haemangioma Rare tumour which presents soon after birth May be associated with intraorbital extension Starts as small, red lesion, most frequently on upper lid Grows quickly during first year Begins to involute spontaneously during second year Blanches with pressure and swells on crying

Periocular haemangioma Treatment options Steroid injection in most cases Surgical resection in selected cases Occasional systemic associations High-out heart failure Kasabach-Merritt syndrome - thrombocytopenia, anaemia and reduced coagulant factors Maffuci syndrome - skin haemangiomas, endrochondromas and bowing of long bones

Histology of capillary haemangioma Lobules of capillaries Fine fibrous septae Lobules under high magnification

Port-wine stain (naevus flammeus) Rare, congenital subcutaneous lesion Segmental and usually unilateral Does not blanch with pressure Associations Ipsilateral glaucoma in 30% Sturge-Weber or Klippel-Trenaunay-Weber syndrome in 5%

Progression of port-wine stain Initially red and flat Subsequent darkening and hypertrophy of skin Skin becomes coarse, nodular and friable

Pyogenic granuloma Cutaneous horn Usually antedated by surgery or trauma Uncommon, horn-like lesion protruding through skin Fast-growing pinkish, pedunculated or sessile mass May be associated with underlying actinic keratosis or squamous cell carcinoma Bleeds easily