Intermediate uveitis: Difference between revisions

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'''Intermediate uveitis''' is a form of [[uveitis]], a group of inflammatory diseases that produces swelling and destroys eye tissues. These diseases can slightly reduce vision or lead to severe vision loss. Intermediate uveitis, also known as pars planitis, is characterized by inflammation of the vitreous and peripheral retina.
== Intermediate Uveitis ==


== Causes ==
[[File:Anterior_vitreous_cells.jpg|thumb|right|Anterior vitreous cells as seen in intermediate uveitis]]
The exact cause of intermediate uveitis is unknown. However, it is often associated with systemic conditions such as [[sarcoidosis]], [[multiple sclerosis]], and [[Behçet's disease]]. It can also occur as an isolated condition with no identifiable cause.


== Symptoms ==
'''Intermediate uveitis''' is a form of [[uveitis]] that primarily affects the [[vitreous body]] and the peripheral [[retina]]. It is characterized by inflammation of the [[pars plana]], the area between the [[ciliary body]] and the [[retina]]. This condition is also known as "pars planitis" when it occurs without an associated systemic disease.
The most common symptoms of intermediate uveitis include [[floaters]], blurred vision, and progressive loss of vision. Other symptoms may include pain, redness of the eye, and sensitivity to light.
 
== Clinical Features ==
 
Intermediate uveitis typically presents with floaters and blurred vision. Patients may also experience mild discomfort or redness in the affected eye. The hallmark of intermediate uveitis is the presence of inflammatory cells in the [[vitreous humor]], which can be observed during an eye examination.
 
=== Symptoms ===
 
* Floaters
* Blurred vision
* Mild eye discomfort
* Redness of the eye
 
=== Signs ===
 
* Vitreous cells and haze
* Snowbanking or snowballs in the peripheral retina
* Possible cystoid macular edema


== Diagnosis ==
== Diagnosis ==
Diagnosis of intermediate uveitis involves a thorough examination of the eye by an [[ophthalmologist]]. This may include a [[fundus examination]], [[fluorescein angiography]], and [[optical coherence tomography]].
 
The diagnosis of intermediate uveitis is primarily clinical, based on the presence of vitreous cells and the exclusion of other causes of uveitis. Ancillary tests such as [[fluorescein angiography]] and [[optical coherence tomography]] (OCT) may be used to assess the extent of retinal involvement and macular edema.
 
== Etiology ==
 
Intermediate uveitis can be idiopathic or associated with systemic diseases such as [[multiple sclerosis]], [[sarcoidosis]], or [[Lyme disease]]. It is important to evaluate patients for these conditions, especially if the uveitis is bilateral or recurrent.


== Treatment ==
== Treatment ==
Treatment for intermediate uveitis aims to reduce inflammation and prevent further damage to the eye. This may involve the use of [[corticosteroids]], [[immunosuppressive drugs]], and in some cases, surgery.
 
The treatment of intermediate uveitis aims to reduce inflammation and prevent complications. Corticosteroids are the mainstay of therapy, administered either topically, orally, or via periocular injections. In cases where corticosteroids are insufficient or contraindicated, immunosuppressive agents such as [[methotrexate]] or [[azathioprine]] may be used.
 
=== Corticosteroids ===
 
* Topical corticosteroids for mild cases
* Oral corticosteroids for more severe inflammation
* Periocular injections for localized treatment
 
=== Immunosuppressive Therapy ===
 
* Methotrexate
* Azathioprine
* Biologic agents in refractory cases


== Prognosis ==
== Prognosis ==
The prognosis for intermediate uveitis varies depending on the severity of the condition and the effectiveness of treatment. With appropriate treatment, most people with intermediate uveitis can maintain good vision.


== See also ==
The prognosis for intermediate uveitis varies depending on the underlying cause and the response to treatment. With appropriate management, many patients can achieve good visual outcomes. However, complications such as [[cataract]], [[glaucoma]], and [[macular edema]] can affect the prognosis.
 
== Related Pages ==
 
* [[Uveitis]]
* [[Uveitis]]
* [[Sarcoidosis]]
* [[Vitreous body]]
* [[Multiple sclerosis]]
* [[Retina]]
* [[Behçet's disease]]
* [[Ciliary body]]
 
{{Uveitis}}


[[Category:Eye diseases]]
[[Category:Inflammatory diseases]]
[[Category:Ophthalmology]]
[[Category:Ophthalmology]]
 
[[Category:Inflammatory diseases of the eye]]
{{stub}}
{{dictionary-stub1}}

Revision as of 16:32, 16 February 2025

Intermediate Uveitis

Anterior vitreous cells as seen in intermediate uveitis

Intermediate uveitis is a form of uveitis that primarily affects the vitreous body and the peripheral retina. It is characterized by inflammation of the pars plana, the area between the ciliary body and the retina. This condition is also known as "pars planitis" when it occurs without an associated systemic disease.

Clinical Features

Intermediate uveitis typically presents with floaters and blurred vision. Patients may also experience mild discomfort or redness in the affected eye. The hallmark of intermediate uveitis is the presence of inflammatory cells in the vitreous humor, which can be observed during an eye examination.

Symptoms

  • Floaters
  • Blurred vision
  • Mild eye discomfort
  • Redness of the eye

Signs

  • Vitreous cells and haze
  • Snowbanking or snowballs in the peripheral retina
  • Possible cystoid macular edema

Diagnosis

The diagnosis of intermediate uveitis is primarily clinical, based on the presence of vitreous cells and the exclusion of other causes of uveitis. Ancillary tests such as fluorescein angiography and optical coherence tomography (OCT) may be used to assess the extent of retinal involvement and macular edema.

Etiology

Intermediate uveitis can be idiopathic or associated with systemic diseases such as multiple sclerosis, sarcoidosis, or Lyme disease. It is important to evaluate patients for these conditions, especially if the uveitis is bilateral or recurrent.

Treatment

The treatment of intermediate uveitis aims to reduce inflammation and prevent complications. Corticosteroids are the mainstay of therapy, administered either topically, orally, or via periocular injections. In cases where corticosteroids are insufficient or contraindicated, immunosuppressive agents such as methotrexate or azathioprine may be used.

Corticosteroids

  • Topical corticosteroids for mild cases
  • Oral corticosteroids for more severe inflammation
  • Periocular injections for localized treatment

Immunosuppressive Therapy

  • Methotrexate
  • Azathioprine
  • Biologic agents in refractory cases

Prognosis

The prognosis for intermediate uveitis varies depending on the underlying cause and the response to treatment. With appropriate management, many patients can achieve good visual outcomes. However, complications such as cataract, glaucoma, and macular edema can affect the prognosis.

Related Pages

Template:Uveitis