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Brain atrophy
How to look at brain atrophy films
Brain atrophy images, in fact, are simple to read, whether it's brain MRI or head CT scans. You'll notice that the brain sulci have become widened, giving the brain a less full appearance, similar to a walnut, a flattened walnut, not very plump, with widened brain sulci and fissures. The brain volume appears smaller, which is typical of brain atrophy images. The treatment for brain atrophy can involve using medications that nourish brain cells and improve cerebral circulation. In terms of dietary therapy, it's beneficial to consume more walnuts and foods that enhance kidney function regularly. According to Traditional Chinese Medicine, the kidney governs the bones and generates marrow, and the brain is considered the sea of marrow; thus, these kidney-nourishing foods are believed to be effective in treating brain atrophy. Foods such as Chinese yam and goji berries can be added to soups or used to make porridge, offering benefits in treating brain atrophy.
Brain atrophy should be treated in the neurology department.
Cerebral atrophy is a type of vascular pathology. Patients need to visit the neurology department of a hospital for examination. Mild cases may lead to a decline in memory, while severe cases can affect intelligence and the ability to live normally. Patients with mild symptoms should timely follow medical advice to choose medications that nourish brain cells, and should also stabilize blood pressure, blood sugar, and blood viscosity. Engaging in intellectual games, exercising brain cells, having family companionship, participating in outdoor exercises to enhance immune capabilities, stabilizing the condition, and undergoing regular follow-ups are also advised.
What are the symptoms of cerebral atrophy?
Some patients with brain atrophy may not exhibit any specific clinical symptoms and are only found to have brain atrophy through imaging studies, such as magnetic resonance imaging (MRI) of the brain. Some patients do exhibit clinical symptoms, and the common symptoms of brain atrophy mainly include the following manifestations. First, patients may experience a decline in memory function, such as frequently forgetting things they have just done, forgetting where they placed their wallet, or forgetting to bring keys when going out. Second, there may also be a decline in executive functions, such as difficulties in dressing or brushing teeth by oneself. Third, there may be a decline in computational abilities, to the extent that the patient cannot perform simple arithmetic. Additionally, brain atrophy may also present some psychiatric symptoms, such as hallucinations and incoherent speech.
Is cerebral atrophy easy to treat?
Brain atrophy, a condition commonly seen in middle-aged and elderly patients, leads to a decline in memory, resulting in symptoms such as forgetfulness, insomnia, and poor mental health. Mild brain atrophy can gradually improve through the use of drugs that nourish brain cells and regular functional exercise. It is advisable to regularly choose drugs that nourish brain cells, eat foods like walnuts, sunflower seeds, and avocados, and engage in intellectual exercises, such as playing chess or playing games that develop intelligence, all of which are effective in treating brain atrophy.
Symptoms of baby brain atrophy
The symptoms of baby brain atrophy include the following: First, the child shows no interest in the surroundings, poor responsiveness, significantly reduced movements, poor sucking ability, and often chokes on milk. Second, the child with brain atrophy exhibits abnormal muscle tone and posture. Symptoms of cerebellar atrophy include difficulty in abducting the thighs, difficulty in extending the knees, legs straightened and adducted when held upright, legs crossed in a scissor-like manner, bent elbow and wrist joints, and the hands often clenched with the thumb turned inward. Third, congenital reflexes are weakened or may not appear at all, such as the rooting reflex, grasp reflex, and embrace reflex, which are either weakened or completely absent. Fourth, there is limited voluntary movement; the baby cannot reach out voluntarily to grab liked objects after five months or always uses one hand to reach for things. Fifth, there are signs of intellectual disability, delayed language development, or language disorders.
Does cerebellar atrophy cause confusion?
Cerebellar atrophy primarily affects the coordination functions of patients, leading to symptoms such as unstable walking and unsteady handling of objects with the hands. This condition does not have a significant connection with human consciousness, and does not affect the reticular structure of the brainstem or the cerebral cortex. Therefore, patients with cerebellar atrophy do not experience confusion or cognitive impairments. If a patient with cerebellar atrophy does exhibit confusion, it is important to consider other possible causes, such as electrolyte disturbances due to poor food intake or concurrent diseases, such as cerebral cortex thrombosis, hemorrhage, or brainstem infarction. It is necessary to conduct additional laboratory tests and cranial magnetic resonance imaging to confirm these conditions.
The difference between cerebral atrophy and cerebellar atrophy.
Whether it is cerebral atrophy or cerebellar atrophy, these are concepts in imaging. They are generally detected through cranial CT or MRI scans, resulting in such diagnoses in imaging reports. Generally, cerebral atrophy mainly refers to the atrophy of the cerebral cortex, which includes areas like the frontal lobe, temporal lobe, hippocampus, and parietal lobe. The cerebral cortex is closely related to cognitive functions, movement, sensation, and emotions of the limbs. Patients with cerebral atrophy typically show a decline in intelligence, slow reactions, and dysfunction of bladder and bowel control, etc. The cerebellum mainly coordinates the body's integrative movements and ensures the fluent execution of limb movements. Therefore, cerebellar atrophy primarily leads to symptoms of ataxia, like finger tremors and unsteady walking.
Is cerebellar atrophy hereditary?
Whether cerebellar atrophy is hereditary depends on the cause of the atrophy. In neurology, there is a disease called spinocerebellar ataxia, which is caused by genetic mutations and results in significant ataxic symptoms. The imaging studies show cerebellar atrophy. This disease can be inherited, so it is important to conduct prenatal counseling to promote eugenics. Cerebellar atrophy caused by other reasons is not hereditary. For example, if the atrophy is due to neurodegenerative disease such as multiple system atrophy, there is no clear genetic tendency. If the atrophy is caused by a cerebellar infarction, it is also not hereditary.
What should I do about brain atrophy?
Brain atrophy includes both physiological and pathological types. Physiological brain atrophy generally occurs as age increases, similar to how wrinkles appear on the face. This type does not usually present symptoms and typically does not require treatment, as some degree of brain shrinkage may happen with age. Pathological brain atrophy, however, can occur in younger individuals and requires investigation to determine the underlying cause. Diagnostic tests should be conducted to clarify the cause of the atrophy and identify any specific diseases, which will guide the treatment plan. Additionally, some patients may experience atrophy due to past events like cerebral hemorrhage or stroke, which are caused by specific lesions. In such cases, treating the original disease is the approach taken, so the treatment plan for brain atrophy should be based on the specific circumstances.