Medical expert of the article
New publications
Central serous chorioretinopathy: causes, symptoms, diagnosis, treatment
Last reviewed: 23.04.2024
All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.
We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.
If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.
Central serous chorioretinopathy is a disease manifested by a serous detachment of the neuroepithelium of the retina and / or pigment epithelium. It has been established that serous detachment can be idiopathic, as well as caused by inflammatory and ischemic processes.
The trigger mechanism in the development of the disease can be stress, and the onset of the disease is due to increased permeability of the Bruch membrane. In the pathogenesis of the disease, great importance is attached to the violation of blood flow velocity and hydrostatic pressure in choriocapillaries, as well as to an increase in the permeability of the walls of the vessels of the choroid. There is no evidence of a hereditary nature of the disease. Central serous chorioretinopathy is widespread throughout the world. Among the diseases prevail in the third to fourth decade of life. The prognosis is favorable, but relapses are often noted.
Symptoms of central serous chorioretinopathy
Patients complain of sudden blurring of vision, the appearance of a dark spot before the eye, a decrease (micropsy) or an increase (macropsia) of objects, a distortion of their shape (metamorphosis) in one eye, a violation of color vision, accommodation. Initial symptoms may not be seen by the patient until the disease manifests in the other eye. In 40-50% of cases, the process is two-sided. The relative safety of visual acuity in the presence of a detachment of pigment epithelium can be explained by the presence of an unclosed neuroepithelium of the retina.
In the early stage of the disease, a focus of an elevated turbid retina with a size of 0.5 to 5 times the diameter of the optic nerve disc appears in the central region. At the edge of the focus, the folding vessels create a rim of the light reflex.
A few weeks later, the origin of the focus decreases, the clouding of the retina disappears. In the place of the hearth there are small yellowish-white spots called precipitates. The visual acuity increases, but co-i is stored relative scotoma in the field of vision. Later, visual acuity is restored, subjective and objective symptoms of the disease disappear, but often the process recurs. After repeated attack of the disease in the macular area, areas of uneven pigmentation remain.
What's bothering you?
What do need to examine?
How to examine?
Treatment of central serous chorioretinopathy
In most cases, self-healing occurs in a few weeks or months. In view of the alleged etiology of the process, dehydration and anti-inflammatory therapy is carried out, steroids are prescribed; Perform also laser photocoagulation to close defects in pigment epithelium.