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Eye diseases. Tumors of the choroid and anomalies of the vascular tract (lecture notes)

Lecture notes, cheat sheets

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LECTURE No. 19. Tumors of the choroid and anomalies of the vascular tract

1. Cysts of the iris

In the iris, single thin-walled or multiple blisters of various shapes and sizes are determined, which grow and can cause secondary glaucoma. If the cysts have a yellowish tint, they are called pearl cysts. They can occur in the iris due to the germination of the corneal epithelium into it after perforated wounds or surgical interventions.

2. Cysts of the ciliary body

Determined by cycloscopy and gonioscopy. At the extreme periphery, at the dentate line, yellow-gray bubbles are visible, protruding into the vitreous body. Ciliary body cysts should be differentiated from retinal detachment, which is characterized by the presence of light gray or pink blisters, retinal swelling, and changes in the course and color of blood vessels. Cysts often cause secondary glaucoma.

Treatment is carried out, as a rule, in the event of secondary glaucoma and consists in diathermocoagulation of the ciliary body, sometimes in excision of the cyst. Iris cysts are treated with diathermo or photocoagulation and excision.

3. Angioma of the choroid

Angiomas are more often localized in the paracentral parts of the fundus, have a round shape, a yellowish-cherry color, and their borders are unclear. According to the location of the angiomas, a defect in the field of view is observed. If angioma of the vascular tract does not grow, it cannot be treated. When angioma grows, it should be differentiated from melanoblastoma. Diagnosis is aided by radioisotope studies and angiography. It should be taken into account that melanoblastoma occurs mainly in adults and elderly people.

4. Pigment tumors

These benign melanomas in children can be localized in different parts of the vascular tract. Benign melanomas ("birthmarks") of the iris are of different sizes, slightly rise above its surface and have a dark color of varying intensity. They usually don't grow.

Melanomas of the ciliary body are almost never detected in vivo and do not cause noticeable changes in the functions of the eye.

Choroidal melanomas are often discovered incidentally during ophthalmoscopy. They look like spots of varying sizes and localization, dark with a gray tint, round in shape, with fairly clear boundaries. The retina under these spots is not changed or, due to the pronounced thickness of the melanoma, is somewhat protruded into the vitreous body. The state of eye function depends on the severity and location of melanomas.

Children with melanomas of the vascular tract are subject to dispensary observation. At the slightest increase in the size of melanoma, radioisotope diagnostics and other additional studies are indicated.

Melanoblastoma of the vascular tract in children is almost never registered. It is more common in people over thirty years of age.

Treatment. Surgical intervention, diathermo, photo or laser coagulation.

5. Neurofibromatosis

If, during examination using lateral illumination and biomicroscopy, the unevenness of the anterior chamber is determined, multiple nodules of a brownish-yellowish round shape with clear boundaries are found in the iris, slightly rising above the surrounding unchanged tissue of the iris, you should find out whether the patient has changes on the skin (pigment spots café-au-lait color, tumors along the skin nerves), which is characteristic of neurofibromatosis, or Recklinghausen's disease.

It must be remembered that in such a patient, an increase in intraocular pressure is possible. Sometimes, in the absence of common clear manifestations of neurofibromatosis, the detection of changes in the organ of vision is of great diagnostic value.

6. Anomalies of the vascular tract

Congenital coloboma of the iris (coloboma iridis congenitum) is the result of non-closure of the slit of the eye cup. The downward direction of the coloboma, the preservation of the sphincter of the pupil and its reaction to light, and sometimes the symmetry of the lesion of both eyes are characteristic. Sometimes it is combined with coloboma of the choroid itself and other malformations. With ophthalmoscopy, the coloboma of the choroid itself appears as a varied shape and size of a white sector with clear edges, over which the retinal vessels pass without change. Choroid coloboma, depending on its location, can cause a decrease in visual functions.

Polycoria (polycoria) multiple pupils. Corectopia (corectopia) displacement of the pupil. Both of these anomalies may be accompanied by a decrease in vision.

Aniridia (aniridia congenita) absence of the iris. In transmitted light, a bright red reflex is recorded. Visual functions are sharply reduced. May be associated with glaucoma. In such cases, surgical treatment of glaucoma is indicated.

Heterochromia is the difference in the color of the irises in the right and left eyes.

Albinism (albinismus) is the absence or deficiency of pigment in the choroid, retinal pigment epithelium, skin, and hair. Often such individuals have pronounced nystagmus and poor vision due to excessive light in the eyes. Wearing smoky glasses is shown.

The residual pupillary membrane (membrana pupillarus perseverans) is the remnants of a film that closes the pupil, which dissolves by the end of uterine life. It has the appearance of thin threads starting from the small arterial circle of the iris or from its surface and attached to the anterior lens capsule. Sometimes, crossing the pupil, the membrane goes to the small arterial circle on the opposite side. Occasionally, the remnants of the pupillary membrane are an accumulation on the anterior capsule of the lens of small pigment clumps, shaped like asterisks.

Author: Shilnikov L.V.

<< Back: Choroiditis

>> Forward: Pathologies of the fundus (part I) (General diagnostic issues. Pigmentary dystrophy (degeneration) of the retina (retinitis pigmentosa). Macular degeneration of the retina (degeneratio maculae luteae). Macular degeneration in Tay Sachs disease. Retrolental fibroplasia. External exudative hemorrhagic retinitis, or Coats disease (retinitis exsudativa haemorrhagica externa Acute obstruction of the central retinal artery (embolia s. thrombosis arteriae centralis retinae). Thrombosis of the central retinal vein (thrombosis venae centralis retinae))

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