Intermediate uveitis is diagnosed when the signs of uveitis are most pronounced in the vitreous, although lesser degrees of inflammation may coexist in the anterior and posterior segments.

Pars planitis is the most common form of intermediate uveitis, and is characterized by inflammatory exudates over the inferior peripheral retina, ora serrata and pars plana. It typically affects young adults and is usually bilateral. The usual clinical course comprises chronic, low-grade inflammation with occasional exacerbations resulting in blurred vision and floaters. Although the etiology is currently unknown, occasional associations with systemic diseases including sarcoidosis, multiple sclerosis, Lyme disease, Whipple’s disease and intraocular lymphoma are well-documented.


Floaters and blurred vision are the principal symptoms. Blurred vision may be due to vitreous infiltrates or cystoid macular edema (CME). Mild symptoms may exist for many months before the patient seeks medical attention. Occasionally, asymptomatic cases of pars planitis are diagnosed on routine examination. Red eye, ocular pain and photophobia are more suggestive of anterior uveitis.


The anterior segment is clear or shows low-grade inflammation only; similarly, there are no focal inflammatory fundus lesions. A variable degree of vitreous haze is usual, with floaters and inflammatory cells in the anterior vitreous.

The critical signs of pars planitis can often be seen only with indirect ophthalmoscopy & scleral depression. White vitreous cellular aggregates (‘snowballs’) form near the ora serrata, usually inferiorly. With disease progression, these lesions organize into a smooth, white, fibrovascular membrane over the inferior pars plana (‘snowbanking’ – the pathognomonic sign in pars planitis). Progressive fibrosis and contraction of this membrane occasionally results in vision-threatening complications including vitreous or retinal detachment, vitreous hemorrhage and neovascularization of the optic disc and peripheral retina.

CME is the most common cause of reduced visual acuity in intermediate uveitis. Chronic, cystoid changes rarely cause permanent visual impairment from lamellar macular hole formation.

Other signs may include mild peripheral periphlebitis, posterior subcapsular cataract (possibly corticosteroid-induced) and elevated intraocular pressure with secondary glaucoma.


Very rare (less than 1 per 100,000).


The majority of patients experience low-grade, chronic inflammation and have a very good visual prognosis without treatment. Nevertheless, potential vision-threatening complications & systemic associations necessitate thorough assessment & review.

Differential Diagnosis

Sarcoidosis, Toxoplasmosis, Toxocariasis, Syphilis, Lyme Disease, Multiple Sclerosis (see Optic Neuritis).

See Also

Posterior Uveitis, Cystoid Macular Edema, Retinal Detachment, Macular Hole.


Blood Tests, Imaging Investigations

Baseline investigations include chest x-ray (hilar lymphadenopathy in sarcoidosis), serum angiotensin-converting enzyme (often elevated in sarcoidosis) and syphilis serology. Serological tests for toxoplasmosis and toxocariasis may also be helpful, depending on the clinical presentation. When multiple sclerosis is suspected, referral to a neurologist is appropriate. Fluorescein angiography is often performed to detect retinal vasculitis. Macular edema can also be assessed by observation, angiography or ocular coherence tomography (OCT).


The principal indication for treatment of pars planitis is impaired visual acuity (often worse than 20/40). The initial treatment is corticosteroids. Posterior sub-Tenon’s injection (e.g., methylprednisolone, at intervals of 1-2 months) is favored in cases of significant vitreous reaction, CME or periphlebitis. Topical corticosteroids are administered for significant or symptomatic anterior chamber inflammation. Oral or intravenous therapy – steroid or other immunosuppressive agents – are generally reserved for resistant cases. Transcleral cryotherapy to the area of snowbanking, pars plana vitrectomy and laser photocoagulation to areas of peripheral neovascularization are also performed occasionally.


Initial review is at 1 to 4 week intervals, then tapered according to severity and response to treatment. 10 percent of cases are self-limited; 90 percent are chronic. Patients receiving prolonged corticosteroid therapy are monitored for elevated intraocular pressure and cataract.

Figure 1.

Pars planitis. Image courtesy of Dr Anthony Hall, Melbourne

Pars Planitis