Orbital disease Flashcards

1
Q

What occurs with soft tissue involvement?

A

Includes lid and periorbital oedema, ptosis and conjunctival swelling due to inflammation or vascular abnormalities

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2
Q

What is proptosis (exophthalmos)?

A

Abnormal protrusion of the globe externally, the protrustion can be intra/extraconal Pseudoproptosis may occur with high myopia or contralateral enophthalmos
Causes: thyroid eye disease, tumours, inflammation, infection

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3
Q

What is enopthalmos?

A

condition in which the globe is recessed within the orbit
Small globe- nanopthalmos, micropthalmos or phthisis bulbi
Structural abnormalities  e.g. blow out fracture
Atrophy of the orbital contents- irradiation or scleroderma

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4
Q

What is ophthalmoplegia?

A

restriction or disability of the ocular muscles
Tumour
Restrictive myopathy- thyroid eye disease (TED) or myositis
Ocular motor nerve lesions
Trauma- longstanding blow out fracture

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5
Q

What are dynamic properties fo the eye?

A

Increased venous pressure- thyroid eye disease or vascular problems
Pulsation- AV communication (+/- bruit) or defect in orbital floor (CSF pulsation & no bruit)
Bruits may be heard with the bell of a stethoscope, it is a sign of carotid-cavernous fistula

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6
Q

What are fungus changes that occur?

A

Optic disc changes, disc swelling, atrophy, opticociliary shunts
Choroidal folds
Retinal vascular changes

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7
Q

What are the common ocular manifestations of thyroid eye disease?

A
Eyelid retraction 
periorbital oedema
Exophthalmos (proptosis) (1/3) (permanent in 70% of cases)
Diplopia (5-10%)
Lid lag when following from superior to inferior position 
Eyelid erythema
Conjunctival injection
Chemosis
Swelling of the caruncle
Eyelid oedema
Optic neuropathy (5%)(perform CT, assess VA, colour vision, papillary reactions, visual fields, fundoscopy)
Restrictive myopathy
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8
Q

What occurs with restrictive myopathy?

A

up to 50% of patients will have a permanent diplopia
oedema is the cause in active stages and fibrosis in later stages
the muscles affected in order of frequency are inferior rectus, media rectus, superior rectus and finally lateral rectus

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9
Q

What are the signs in orbital cellulitis?

A
infection located behind the orbital septum, usually secondary to ethmoiditis 
severe malaise, fever 
Severe orbital oedema
Redness
Ptosis
Painful ophthalmoplegia
Optic nerve dysfunction, if advanced
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10
Q

What are the complications of orbital cellulitis?

A

Optic neuropathy and abscess formation, in severe cases this can lead to infection of the cranial cavity (raised IOP, retinal vasculature occlusion)

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11
Q

What is idiopathic orbital inflammatory disease (IOID)?

A

A non-neoplastic, non-infectious orbital lesion and can involve any soft tissue component, presentation is typically between 20-50 years and with an abrupt painful
onset
Usually unilateral with proptosis, chemosis, periorbital swelling and ophthalmoplegia- this is a diagnosis of exclusion

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12
Q

What are the vascular orbital disorders?

A
Orbital venous anomalies (varices):
Isolated orbital varices
Combined orbital & external varices
Carotid-cavernous fistula:
Direct/Indirect
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13
Q

What are orbital venous varies?

A

Usually unilateral and may bleed or become thrombosed These patients will demonstrate intermittent proptosis accentuated by the Valsalva manoeuvre

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14
Q

What is a direct carotid-cavernous fistula?

A

Abnormal communications between the carotid artery and cavernous sinus
This is a high velocity flow shunt, causes include head trauma or spontaneous rupture
Pulsatile proptosis with bruit and thrill- abolished by ipsilateral carotid compression there is retinal venous congestion and haemorrhage
Ptosis
Chemosis
Conjunctival injection
Ophthalmoplegia
Raised IOP

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15
Q

What is an indirect carotid-cavernous fistula?

A
Abnormal indirect communications between meningeal branches of the internal carotids and the cavernous sinus, these are mostly congenital malformationor spontaneous rupture 
Dilated episcleral vessels
Raised IOP
Occasional ophthalmoplegia
Mild proptosis
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16
Q

What are encephaloceles?

A

Herniation of intracranial contents through the congenital skull defect
Meningocele contains only dura and a meningoencephalocele contains dura and brain tissue- transmission of CSF will cause a pulsatile proptosis without a bruit

17
Q

What re the types of orbital tumours?

A

Vascular tumours- capillary or cavernous haemangioma
Lacrimal gland tumours- pleomorphic adenoma
Neural tumours-noptic nerve glioma or optic never sheath meningioma
Miscellanous tumours- metastases or invasion from sinuses

18
Q

What are cavernous haemangiomas?

A

the most common adult orbital benign tumour- found just behind the globe
They are most common in women 40-60
treatment is surgical excision

19
Q

What are capillary haemangiomas?

A

The most common orbital tumour in children with 30% present a birth and 100% present by 6 months of age- these tumours may enlarge on coughing or straining These are associated with systemic conditions (high output cardiac failure, Maffuci syndrome etc) Growth is during the 1st year and 70% have resolved by age 7
Treated with steroid injections, systemic steroids and local resection if possible

20
Q

What are pleomorphic lacrimal gland adenomas?

A

Present in the 4th to 5th decades and are painless and slow growing
These tumours are well encapsulated so can be surgically removed

21
Q

What are lacrimal gland carcinomas?

A

Present in the 4th to 6th decades and have a very poor prognosis
Painful and grow rapidly Diagnosis is by biopsy and treatment is radical surgery and radiotherapy

22
Q

What are optic nerve gliomas?

A

Typically affect young girls and are associated with NF-1 Present at end of 1st decade with gradual visual loss
Slow growing lesions can be observed, but excision is necessary if affecting vision or cosmesis

23
Q

What are optic nerve sheath meningiomas?

A

Typically affects middle aged women and causes gradual visual loss to due optic nerve compression
treatment depends on the tumour, but excision and radiotherapy may be necessary

24
Q

Where do metastatic tumours to the orbit commonly spread from?

A
Breast
Bronchus
Prostate
Skin melanoma 
GI tract 
Kidney
25
Q

What is the treatment for orbital cellulitis?

A
Systemic antibiotics and monitoring of optic nerve function 
Indications for surgery:
Resistance to antibiotics
Orbital or subperiosteal abscess
Optic neuropathy
26
Q

What is the treatment for idiopathic orbital inflammatory disease?

A

has a varying outcome from mild to severe
Early spontaneous remission without sequelae- no treatment
Prolonged intermittent activity with eventual remissions, treatment options steroid therapy, radiotherapy and cytotoxic usage
Severe prolonged activity causing a ‘frozen orbit’