Myasthenia Gravis Surgical Treatment

Written by Xie Wen
Neurology
Updated on March 20, 2025
00:00
00:00

Myasthenia gravis is an autoimmune disease, with many patients also having a thymoma. The thymus is a very important immune organ in humans, and abnormal proliferation of the thymus can produce acetylcholine receptor antibodies. These antibodies circulate to the neuromuscular junction and participate in the antigen-antibody reaction, leading to the onset of myasthenia gravis. By removing the thymus, the initiating antigens of the patient's autoimmune response can be eliminated, reducing the involvement of T cells, B cells, and cytokines in the autoimmune response. This surgery is suitable for patients with thymic hyperplasia and high acetylcholine receptor antibody titers, or those with various types of myasthenia gravis with thymoma, as well as young women with generalized myasthenia gravis, and those who are dissatisfied with cholinesterase inhibitor treatment. About 70% of patients can experience symptom relief or complete recovery after surgery.

Other Voices

doctor image
home-news-image
Written by Zhang Hui
Neurology
56sec home-news-image

How to treat myasthenia gravis?

Myasthenia gravis falls under the category of neurological diseases, characterized as an immune disorder of the nervous system, primarily due to the presence of antibodies against acetylcholine receptors. This leads to impaired transmission of nerve impulses to muscles, resulting in various clinical symptoms. The treatment approaches for myasthenia gravis include the following. Firstly, the use of cholinesterase inhibitors is recommended. These medications increase acetylcholine levels and are effective in improving symptoms. Secondly, patients are treated with corticosteroids, typically starting with a low dose and gradually increasing to maintain for a period before reducing the dose again. Adjustments to medication should always be made under the guidance of a neurologist. Third, if the patient has a thymoma, surgical removal is advised.

doctor image
home-news-image
Written by Zhang Hui
Neurology
56sec home-news-image

What is myasthenia gravis?

Myasthenia gravis is a group of neuromuscular junction disorders and is also an autoimmune disease of the nervous system. It primarily involves the production of certain antibodies in the body that attack the acetylcholine receptors on the postsynaptic membrane of the neuromuscular junction. This results in the inability of nerve impulses to be effectively transmitted to the muscles, causing the muscles to lose neural control, leading to weakness of the limbs. This weakness is typically more pronounced in the evening than in the morning, with symptoms being lighter upon waking and worsening in the afternoon. As the disease is caused by an autoimmune response, a major focus of treatment is to suppress this abnormal immune reaction, primarily through the administration of corticosteroids. Additionally, many patients with myasthenia gravis also exhibit thymus abnormalities, necessitating thorough CT examinations of the thymus.

doctor image
home-news-image
Written by Liu Hong Mei
Neurology
56sec home-news-image

What should people with myasthenia gravis pay attention to in their daily lives?

Patients with myasthenia gravis should be careful to continue taking their medications after being discharged from the hospital and must not change the dosage or administration of their medication on their own. It is important to avoid overexertion and emotional stimuli in daily life. One should ensure to get enough rest, maintain adequate sleep, and consume fresh vegetables and fruits. Avoid spicy, stimulating, and excitatory foods. Do not be overly sad or experience excessive emotional fluctuations. Pay attention to the risk of catching a cold and upper respiratory infections. Take precautions against exposure to cold and prevent infections. Balance work and rest, maintain regular life patterns, keep in good spirits, ensure adequate sleep, and avoid excessive emotional disturbances and stimuli.

doctor image
home-news-image
Written by Tang Bo
Neurology
48sec home-news-image

Myasthenia Gravis Best Treatment

The treatment of myasthenia gravis should also be individualized, specifically based on the actual condition of the patient. First and foremost, a clear diagnosis is essential. Once the diagnosis is confirmed, cholinesterase inhibitors can be used, but the dosage and frequency must be decided based on the patient's individual condition. Additionally, if the patient has a thymoma or thymic hyperplasia, a surgeon should determine whether surgical treatment is necessary. It is also necessary to consider whether to use steroids or plasmapheresis. In the event of a myasthenic crisis, symptomatic treatment should be provided according to the situation to maintain the patient's vital signs, and it is crucial to diagnose and treat early.

doctor image
home-news-image
Written by Zhang Hui
Neurology
52sec home-news-image

Where should I go for treatment of myasthenia gravis?

Myasthenia gravis is classified as a neurology disease. Therefore, patients should visit the neurology department for medical consultation. Fundamentally, it is an immune disorder of the nervous system characterized by the production of abnormal antibodies. These antibodies affect the acetylcholine receptors on the postsynaptic membrane, thereby impacting the transmission of nerve impulses at the neuromuscular junction, which leads to various clinical symptoms. Patients may experience ptosis, double vision, and potentially compromised swallowing function, causing overall weakness. Symptoms typically worsen towards the evening. Many patients also present with thymus abnormalities. Treatment generally involves oral medications, predominantly corticosteroids and cholinesterase inhibitors.