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

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Optic nerve glioma

Typically affects young girls

Associated neurofibromatosis -1 is common

Presents - end of first decade with gradual visual loss

 

 

Gradually progressive proptosis

Optic atrophy

 

 

Treatment

Observation - no growth, good vision and good cosmesis

Excision - poor vision and poor cosmesis

Radiotherapy - intracranial extension

Optic nerve sheath meningioma

Typically affects middle-aged women

Gradual visual loss due to optic nerve

Optociliary shunts in

compression

30%

Proptosis due to intraconal spread

Thickening and

calcification on CT

 

Treatment

Observation - slow-growing tumours

Excision - aggressive tumours and poor vision

Radiotherapy - slow-growing tumours and good vision

Sphenoidal ridge meningioma

Presents with gradual visual loss and reactive hyperostosis

 

 

 

Proptosis

Fullness in temporal fossa

Hyperostosis on plain x-ray

 

 

 

Lymphoma

Presents - 6th to 8th decades

 

 

 

Affects any part of orbit and

Anterior lesions are rubbery

May be confined to

may be bilateral

on palpitation

lacrimal glands

 

 

 

Treatment

Radiotherapy - localized lesions

Chemotherapy - disseminated disease

Rhabdomyosarcoma

Most common primary childhood orbital malignancy

Rapid onset in first decade ( average 7 yrs )

 

 

May involve any part of orbit

Palpable mass and ptosis in about 30%

 

 

Treatment

Radiotherapy and chemotherapy

Exenteration for radio-resistant or recurrent tumours

Childhood metastatic tumours

Neuroblastoma

Chloroma

Presents in early childhood

Presents at about age 7yrs

May be bilateral

Rapid onset proptosis - may be bilateral

Typically involves superior orbit

Subsequent systematic dissemination to

 

 

 

full-blown leukaemia

Adult metastatic tumours

Common primary sites - breast, bronchus, prostate, skin melanoma, gastrointestinal tract and kidney

Presentations

Anterior orbital mass with non-

Enophthalmos with schirrous

axial globe displacement

tumours

Similar to orbital pseudo-tumour

Cranial nerve involvement at orbital

apex and mild proptosis

 

Orbital invasion by sinus tumours

Maxillary carcinoma

Ethmoidal carcinoma

Upward globe displacement and epiphora

Lateral globe displacement

OPTIC NEUROPATHIES

1.Clinical features

2.Special investigations

3.Optic neuritis

Retrobulbar neuritis

Papillitis

Neuroretinitis

4.Anterior ischaemic optic neuropathy (AION)

5.Leber hereditary optic neuropathy

Signs of optic nerve dysfunction

Reduced visual acuity

Afferent pupillary conduction defect

Dyschromatopsia

Diminished light brightness sensitivity

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