Retinitis Pseudoalbuminuric Stellate

Retinitis Pseudoalbuminuric Stellate: Characteristics and treatment

Retinitis pseudoalbuminurica stellata is a rare disease that affects the retina of the eye. This condition is characterized by the formation of a special type of inflammatory changes in the retina, which can affect vision and lead to serious complications.

Characteristic:
Retinitis pseudoalbuminuric stellate gets its name because of the special form of inflammatory foci that resemble stars and form in the retina. These foci of inflammation are caused by the peculiarities of metabolism in the tissues of the eye and lead to disruption of the normal structure and function of the retina.

Symptoms of pseudoalbuminuric stellate retinitis may include:

  1. Gradual decrease in visual acuity.
  2. The appearance of flickering, flashes or spots before the eyes.
  3. Distortion or loss of central vision.
  4. The appearance of dark spots or a “veil” in front of the eye.

Causes and treatment:
The reasons for the development of pseudoalbuminuric stellate retinitis are not yet fully understood. However, genetic factors and metabolic disorders are believed to influence the development of this disease. Diagnosis is based on examination of the eye, including examination with special instruments such as an ophthalmoscope.

Treatment for pseudoalbuminuric stellate retinitis is aimed at managing symptoms and preventing disease progression. In some cases, laser therapy may be needed to destroy inflammation and prevent further damage to the retina. Medications may also be used to reduce inflammation and maintain eye health.

It is important to note that pseudoalbuminuric stellate retinitis requires regular monitoring by an ophthalmologist and timely seeking medical help. Early detection and treatment of this condition can help prevent serious complications and preserve vision.

Conclusion:
Retinitis pseudoalbuminurica stellate is a rare condition that can have a significant impact on visual function. Proper diagnosis and timely treatment are key aspects of managing this condition. Patients with suspected retinitis pseudoalbuminurica stellate should contact an ophthalmologist for examination and appropriate medical care.

It is also important to understand that this article provides general information about retinitis pseudoalbuminurica stellate and is not a substitute for consultation with an experienced healthcare professional. If you experience any symptoms or questions regarding your health, it is recommended that you consult a qualified healthcare provider for a personalized assessment and advice.



Retinitis pseudobulinica stellato-atrophicans is a rare eye disease characterized by chronic neovascular chorioretinal dystrophy leading to vision loss. Clinical manifestations include narrowing of the visual fields, peripheral anterior myopia, decreased visual acuity, and the presence of stellate lesions in the macular area.

This disease is associated with damage to the choroid and drainage system of the vitreous body. Retinitis is accompanied by hyperfixation of melanin pigment and tissue swelling, which leads to difficulty in the penetration of light rays into the retina. In this regard, problems with vision arise; it manifests itself in the form of a narrowing of the field of vision and dark spots in the upper and lower parts of the field of vision.

The main diagnostic method is optical coherence tomography of the retina, which allows you to determine the presence of edema, star spots, as well as changes in the volume of the vitreous and a subluxated lens. It may also be necessary to perform a Doppler ultrasound examination of the vessels of the fundus to assess the disturbance of blood flow in the vessels of the retina and choroid of the eyes.

Treatment includes local use of anti-inflammatory drugs (for example, cyclooxygenase inhibitors), oral drugs to normalize intraocular pressure and stimulate reparative processes in the vascular tract of the eye. Intravitreal injections of anti-VEGF drugs may also be used to reduce retinal detachment. Surgical treatment such as laser photocoagulation and intravitrectomy is indicated when