12 conjunctival tumours

12
1. Benign Naevus Papilloma Epibulbar dermoid Lipodermoid 2. Pre-malignant Primary acquired melanosis ( PAM ) Intraepithelial neoplasia (carcinoma in situ) 3. Malignant Melanoma Squamous cell carcinoma Kaposi sarcoma Lymphoma CONJUNCTIVAL TUMOURS

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Page 1: 12 conjunctival tumours

1. Benign• Naevus• Papilloma• Epibulbar dermoid• Lipodermoid

2. Pre-malignant• Primary acquired melanosis ( PAM )• Intraepithelial neoplasia (carcinoma in situ)

3. Malignant• Melanoma• Squamous cell carcinoma• Kaposi sarcoma• Lymphoma

CONJUNCTIVAL TUMOURS

Page 2: 12 conjunctival tumours

Naevus

• 30% are almost non-pigmented

• Most frequently juxtalimbal• Sharply demarcated and slightly elevated

• Presents in first two decades

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PapillomaPedunculated Sessile

• Presents in middle age• Not caused by infection• Single and unilateral

• Presents in childhood or early adulthood• Infection with papilloma virus • May be multiple and bilateral

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• Presents in childhood• Smooth, soft mass• Usually juxtalimbal

• Occasionally Goldenhar syndrome

Epibulbar dermoidSigns Association

Page 5: 12 conjunctival tumours

Lipodermoid

• Presents in adulthood• Soft, movable, subconjunctival mass• Most frequently at outer canthus

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Intraepithelial neoplasia(carcinoma in situ)

• Juxtalimbal fleshy avascular mass

• May become vascular and extend onto cornea

• Presents in late adulthood

• Malignant transformation is uncommon

Signs Progression

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Primary acquired melanosis (PAM)

• PAM without atypia is benign• PAM with atypia is pre-malignant • Unilateral, irregular areas of flat,

brown pigmentation• May involve any part of conjunctiva

• Presents in late adulthood

Signs Types

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Conjunctival melanoma

From PAM with atypia

• Sudden appearance of nodules in PAM

From naevus

• Sudden increase in size or pigmentation

Primary

• Solitary nodule• Frequently juxtalimbal but may be anywhere

• Very rare• Most common type

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Localized tumour

• Excision

Treatment of conjunctival melanoma

Diffuse tumour

• Excision of nodules

Orbital recurrence

• Excision and radiotherapy• Adjunctive cryotherapy or

mitomycin C • Exenteration• Adjunctive cryotherapy

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Squamous cell carcinoma

• Rarely metastasizes

• Arises from intraepithelial neoplasia or de novo

• Frequently juxtalimbal

• Slow-growing

• Presents in late adulthood• May spread extensively

Signs Progression

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Kaposi sarcoma

• Most frequently in inferior fornix

• Affects patients with AIDS• Vascular, slow-growing tumour of low malignancy• Very sensitive to radiotherapy

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Lymphoma

• Salmon-coloured, subconjunctival infiltrate

• Usually presents in adulthood• Benign or malignant