Arachnoidendotheliomatosis [Arachnoidendotheliomatosis; Arachnoidendothelioma (Base Arachnoidendotheliomat-) + -Oz; Syn. Meningoteliomato]

Arachnoidendotelliomatosis is a pathological condition characterized by the development of multiple meningiomas of the spinal cord and brain, and caused by genetic and other etiological factors.

The main symptom of arachnoididotellomatosis is recurrent headache, which may be accompanied by visual and hearing impairment. Muscle spasms, nausea and vomiting, increased sensitivity to light, dizziness, balance and memory problems may also occur.

Diagnosis of arachnididotelematoses is based on MRI or CT scans of the brain and spine, as well as additional examinations such as chest x-ray, ultrasound of the liver and electrocardiogram

Arachnoidendotheliomotosis is a rare disease that is characterized by the development of multiple tumors of the meningeal membranes of the brain and spinal cord, also known as meningiosis.

This disease is often combined with other forms of brain tumors and can be diagnosed even at an early stage of its development. It can have various forms of manifestation, including headache, weakness, tinnitus and other neurological disorders.

The causes of this pathology may include genetic factors, exposure to harmful substances on the body, infections, injuries, viral diseases and many other factors. A characteristic sign of the disease is the presence of multiple menigigan histol hyal, which can