Optic neuritis
From Wikipedia, the free encyclopedia
| ICD-10 | H46. |
|---|---|
| ICD-9 | 377.3 |
| DiseasesDB | 9242 |
| MedlinePlus | 000741 |
| eMedicine | radio/488 |
Optic neuritis (or retrobulbar neuritis) is the inflammation of the optic nerve that may cause a complete or partial loss of vision.
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[edit] Causes
The optic nerve comprises axons that emerge from the retina of the eye and carry visual information to the primary visual nuclei, most of which is relayed to the occipital cortex of the brain to be processed into vision.
Inflammation of the optic nerve causes loss of vision usually due to the swelling and destruction of the myelin sheath covering the optic nerve.
Direct axonal damage may also play a role in nerve destruction in many cases.
The most common etiology is multiple sclerosis, 74% of females and 34% of males. [1]
Some other causes include viral-bacterial infections (e.g. herpes zoster), autoimmune disorders (e.g. lupus) and the inflammation of vessels (vasculitis) nourishing the optic nerve.
[edit] Symptoms
Major symptoms are sudden loss of vision (partial or complete), or sudden blurred or "foggy" vision, and pain on movement of the affected eye. Many patients with optic neuritis may lose some of their color vision in the affected eye, with colours appearing subtly washed out compared to the other eye.
On medical examination the head of the optic nerve can easily be visualised by an ophthalmoscope; however frequently there is no abnormal appearance of the nerve head in optic neuritis, though it may be swollen in some patients. In many cases, only one eye is affected and patients may not be aware of the loss of color vision until the doctor asks them to close or cover the healthy eye.
Ethambutol, an antitubercular drug, can also cause optic neuritis
[edit] Treatment and Prognosis
In most cases, visual functions return to near normal within 8 to 10 weeks, but they may also advance to a complete and permanent state of visual loss.
Therefore, systemic intravenous treatment with corticosteroids, which may quicken the healing of the optic nerve, prevent complete loss of vision, and delay the onset of other multiple sclerosis symptoms, is often recommended. It has been demonstrated that oral administration of corticosteroids in this situation may lead to more recurrent attacks than in non-treated patients (though oral steroids are generally prescribed after the intravenous course, to wean the patient off the medication). This effect of corticosteroids seems to be limited to optic neuritis and has not been observed in other diseases treated with corticosteroids.
Very occasionally, if there is concomitant increased intracranial pressure the sheath around the optic nerve may be cut to decrease the pressure.
When optic neuritis is associated with MRI lesions suggestive of multiple sclerosis (MS) then general immunosuppressive therapy for MS is most often prescribed (IV methylprednisolone may shorten attacks; oral prednisone may increase relapse rate).
[edit] Diagnosis
Optic neuritis is often diagnosed by the neurologist and managed by an ophthalmologist. However, ideally, a neuro-ophthalmologist should be consulted at a major university hospital center.
