
We can classify the orbital pathology as:
1. Post-Traumatic pathology:
1.1 Orbital wall fractures
The orbit is delimited by four bony walls, the superior, medial, inferior and lateral, consisting of a total of eight bones. They are classified according to the involvement or not of the orbital rim, and in the absence of involvement, of the displacement of the bony fragments outwards or into the orbit (blow-out and blow-in respectively). [1]

In these cases it is important to describe the type of fracture, if there is herniation of the orbital fat through the fracture or if there is entrapment of the extraocular muscles, as well as to evaluate possible eye involvement (breakage, haematomas, foreign bodies...). Other post-traumatic findings to rule out include carotid-cavernous fistula, discussed below. [2]

1.2 Globe rupture
Ocular trauma is the main cause of visual acuity loss in young individuals. One of its possible outcomes is globe rupture, an ophthalmological emergency. In blunt trauma ruptures are most common immediately following insertion of the rectus muscles. [3]

A number of different findings are identified in CT:
- Loss of the rounded morphology of the eyeball (flat tyre)
- Presence of foreign bodies or intraocular gas
- Thickening of the posterior sclera
- Blurring of the eyeball margins
1.3 Orbital foreign body
A thorough evaluation is necessary to rule out foreign bodies, as their density varies greatly depending on their composition from >1000 HU (metal or glass) to -600 HU (wood). [4]
2. Tumoral:
Orbital masses have a wide differential, and a correct description of the tumour is essential to narrow it down to the most probable pathologies. They can be classified into three main compartments: intraconal, extraconal and intraocular.
2.1 Lymphoma
Primary ocular lymphoma is the most common orbital tumour, accounting for up to 50% of malignant orbital lesions. It usually affects people between 50 and 70 years of age, with a predilection for the female sex, and up to 17% of cases are bilateral. [5]

In imaging: CT scans show a homogeneous, isodense or slightly hyperdense mass with the extraocular musculature and discrete enhancement after contrast administration. MRI shows similar characteristics to cerebral lymphomas:
- T1: iso/hypointense with respect to the muscles, and with homogeneous enhancement after gadolinium administration
- T2: iso/hyperintense with respect to the muscles
- DWI/ADC: diffusion restriction
2.2 Melanoma
Orbital melanoma may be primary, due to local extension from the uvea, conjunctiva or eyelid, or due to metastatic disease. Primary melanomas are extremely rare (<1% of orbital neoplasms), as opposed to uveal melanomas (which represent the most frequent primary intraocular tumour). They account for up to 20% of secondary/metastatic tumours of the orbit. [6]

Imaging: CT scan shows masses with increased attenuation and enhancement after contrast administration. On MRI:
- T1: hyperintense due to previous haemorrhages and melanin content. After gadolinium administration they show enhancement
- T2: hypointense
- SWI/T2*: susceptibility artefacts due to previous haemorrhages
2.3 Optic nerve glioma
They are rare tumours that usually affect children with neurofibromatosis type 1. They are even rarer in adults, in whom they are not related to neurofibromatosis and are more aggressive. [7]

On imaging they appear as a thickening of the optic nerve (fusiform or exophytic). MRI imaging shows:
- T1: iso/hypointense with respect to the contralateral, with variable enhancement after contrast administration
- T2: show central hyperintensity with a thin peripheral hypointense layer (dura mater)
2.4 Orbital meningioma
Orbital meningiomas can be:
- Primary, rare, most of these are optic nerve sheath meningiomas (≈20%)
- Secondary, the most frequent, caused by extension of an intracranial meningioma into the orbit
They are usually diagnosed in women in the fourth decade of life, although up to 25% are diagnosed in childhood, and these tend towards more aggressive behaviour. In imaging, they behave similarly to intracranial ones, with two characteristic signs being the tram-track and the doughnut, observed in sagittal and coronal reconstructions, respectively. [8]

2.5 Other metastases
They are rare, with the uveal ones being more frequent than the extraocular ones. The most frequent primary cancers are breast and lung cancer. Their appearance is variable on imaging.

3. Inflamatory / Infectious:
3.1 Tolosa-Hunt Syndrome
Tolosa-Hunt Syndrome is defined as an idiopathic granulomatous inflammation of the cavernous sinus or superior orbital fissure. Clinically, it presents as painful paralysis of the third cranial nerve (although it can affect any nerve in the cavernous sinus). Peak incidence is around 40 years of age. [9]

CT scan shows asymmetry of the cavernous sinus which may show enhancement. On MRI:
- T1: iso/hyperintense with respect to the muscles. May show gadolinium uptake in the acute phase
- T2: hyperintense
3.2 Dacryocystitis
Dacryocystitis is inflammation of the nasolacrimal sac, due to obstruction of its drainage with secondary infection. It shows two peaks of incidence, in neonates with congenital defects and in the fourth decade of life. Imaging allows us to rule out complications such as abscesses or orbital cellulitis. CT shows fat striation in the inner canthus +/- enhancement. [10]

3.3 Preseptal and postseptal cellulitis
Preseptal and postseptal cellulitis are two diseases that must be differentiated. Their difference lies in whether the involvement is superficial or deep to the orbital septum.



3.4 Optic Neuritis
Its aetiology is divided into infectious and non-infectious, the latter being the most frequent. It generally affects people around 35 years of age, being more frequent in women.


4. Vascular pathology:
4.1 Carotid-cavernous fistula
They are an abnormal communication between the carotid circulation and the cavernous sinus. They can be classified in various ways, the vascular anatomy being the most commonly used, being direct or indirect:
- Direct: direct communication between the internal carotid and cavernous sinus
- Indirect: communication through one of the branches of the carotid circulation (internal or external) and the cavernous sinus
The direct ones are usually post-traumatic, of rapid evolution and in young men, while the indirect ones are usually insidious, secondary to predisposing conditions (Ehlers-Danlos for example) and in post-menopausal women.

On CT we can see indirect findings such as proptosis, oedema of the orbital fat, enlargement of the extraocular musculature, as well as swelling of the cavernous sinus and arterial enhancement of the ophthalmic vein and the cavernous sinus. [13]
It is important to suspect this pathology in certain traumas, as it is important to diagnose it because of possible complications.

4.2 Orbital varicose veins
It is the dilatation of the orbital veins, which can be classified as primary or secondary. Primary varicose veins are idiopathic while secondary varicose veins appear due to an increase in blood flow (due to arteriovenous malformations, carotid-cavernous fistulas, etc.). They are usually asymptomatic, although they may debut in young adults with discomfort, proptosis or intermittent diplopia.In the case of suspicion, a CT scan with Valsalva can be performed with contrast administration, with the consequent dilation and enhancement of the pathologic vein. [14]

5. Miscellaneous:
5.1 Posterior dislocation of intraocular lens
It is a rare complication of cataract surgery. They are usually atraumatic (unlike ectopia lentis) within the first 3 months after surgery. May present as vision loss and may be complicated by retinal detachment. [15]

5.2 Myopia magna, coloboma and staphyloma
They are different forms of eye enlargement, which differ in some details (see figure 20). [16]

5.3 Intra-ocular silicone oil
Used as a substitute for vitreous humour in some retinal detachment operations, it may simulate vitreous haemorrhage by imaging. [17]
