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Ординатура / Офтальмология / Английские материалы / Illustrated Tutorials in Ophthalmology Kanski, Bolton 2001

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Posterior encephalocele

 

 

Caused by congenital defect in

Globe displacement forward and

sphenoid bone

downward

 

 

Associations of encephaloceles

Ocular

Other congenital bony Neurofibromatosis - 1

 

defects

Colobomas

Hypertelorism

Common in posterior

encephalocele

 

Morning glory anomaly

 

Hare lip and cleft palate

 

ORBITAL TUMOURS

1.Vascular tumours

Capillary haemangioma

Cavernous haemangioma

2.Lacrimal gland tumours

Pleomorphic adenoma

Carcinoma

3.Neural tumours

Optic nerve glioma

Optic nerve sheath meningioma

Sphenoidal ridge meningioma

4.Miscellaneous tumours

Lymphoma

Rhabdomyosarcoma

Metastases

Invasion from sinuses

Capillary haemangioma

Most common orbital tumour in children

Presents - 30% at birth and 100% at 6 months

Most commonly in superior anterior orbit

May enlarge on coughing or straining

Associated ‘strawberry’ naevus is common

Capillary haemangioma

 

Natural history

 

Systemic associations

 

 

 

 

 

 

High output cardiac failure

 

 

Kasabach-Merritt syndrome -

 

 

 

thrombocytopenia, anaemia

 

 

Maffuci syndrome - skin

 

 

 

haemangiomas, enchondromata

 

 

 

 

 

 

 

Treatment

 

 

 

 

 

 

Steroid injections - for superficial

 

 

 

component

 

 

Systemic steroids

 

 

Local resection - difficult

Growth during first year

 

 

Subsequent resolution -

 

 

 

complete in 70% by age 7 years

 

 

 

 

 

 

Cavernous haemangioma

Most common benign orbital tumour in adults

Usually located just behind globe

Female preponderance - 70%

Presents - 4th to 5th decade

 

 

Slowly progressive axial proptosis

May cause choroidal folds

 

 

Treatment - surgical excision

Classification of lacrimal gland tumours

( )

Pleomorphic Lacrimal Gland Adenoma

Presents - 4th to 5th decade

 

 

 

 

 

Painless and very slow-

Posterior extension may

Smooth, encapsulated

 

growing, smooth mass in

cause proptosis and

 

outline

 

lacrimal fossa

ophthalmoplegia

Excavation of lacrimal gland

Inferonasal globe

 

 

fossa without destruction

 

displacement

 

 

 

 

 

 

 

 

Technique of surgical excision

Biopsy is contraindicated

Prognosis - good if completely excised

Incision of temporal muscle and periosteum

Removal of lateral orbital wall and dissection of tumour

Drilling of bone for subsequent wiring

Repair of temporal muscle and periosteum

Lacrimal gland carcinoma

Presents - 4th to 6th decades

Very poor prognosis

 

 

 

 

Painful, fast-growing mass in

Posterior extension may cause proptosis,

 

lacrimal fossa

 

ophthalmoplegia and episcleral congestion

Infero-nasal globe displacement

Trigeminal hypoaesthesia in 25%

 

 

 

 

Management

Biopsy

Radical surgery and radiotherapy

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