Myasthenia gravis initial symptoms

Written by Tang Bo
Neurology
Updated on September 29, 2024
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Myasthenia gravis is characterized by fluctuating and fatigue-prone muscle weakness in certain specific striated muscles. Symptoms are generally milder in the morning and more severe in the evening, worsening with continued activity and alleviating after rest.

The most common initial symptom is weakness of the external eye muscles, primarily presenting as asymmetrical ptosis (drooping of the upper eyelid) or narrowing of the eye slit, along with diplopia, which refers to seeing double images. These are the most frequent initial symptoms, seen in over 50% of patients with myasthenia gravis.

Additionally, some patients may experience disturbances in eye movement, facial muscle weakness, air leakage when puffing cheeks, incomplete eyelid closure, shallower nasolabial folds, as well as difficulty swallowing, speech articulation issues, choking while drinking, and potentially severe respiratory weakness.

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Written by Zhang Hui
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Can myasthenia gravis be cured completely?

Myasthenia gravis is a relatively common disease in neurology. Whether it can be completely cured mainly depends on the severity of the disease and some of its subtypes. For instance, patients with ocular myasthenia gravis only exhibit symptoms such as ptosis; by using some corticosteroids or acetylcholinesterase inhibitors, some patients can be cured. However, there are also patients who experience generalized muscle weakness, which is particularly severe and may even affect the respiratory muscles. These patients need long-term or even lifelong medication to prevent the recurrence of severe myasthenia gravis. Additionally, some patients with myasthenia gravis also have thymomas, and many patients can be cured after the removal of the thymoma. Therefore, most cases of myasthenia gravis cannot be completely cured and require long-term medication, though a small portion might be curable.

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What should I do if myasthenia gravis causes difficulty swallowing?

Myasthenia gravis primarily manifests as an inability to swallow, affecting the pharyngeal muscles or the muscles involved in swallowing. Thus, difficulty in swallowing is also a symptom of myasthenia gravis. At this time, the main treatment should focus on the primary disease, administering medications such as neostigmine for myasthenia gravis, and using steroids or immunosuppressants in severe cases. If there is difficulty in swallowing, or if it persists for more than two or three days, a gastric tube can be inserted for nasal feeding to maintain nutrition. Then, as the symptoms of myasthenia gravis subside with medication, swallowing function can recover.

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Written by Zhang Hui
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What should I do if myasthenia gravis is accompanied by a fever?

Patients with myasthenia gravis are most afraid of developing a fever, as a fever may indicate an infection, especially a bacterial infection. If a bacterial infection occurs, it can easily trigger a myasthenic crisis. The patient may experience weakness in breathing and even respiratory failure, which can be life-threatening. Therefore, it is essential to address the situation promptly. The recommended approach when a fever occurs is as follows: First, quickly determine the cause of the fever, complete routine blood tests, calcitonin, and other relevant assays to confirm if it is caused by a bacterial infection. Second, symptomatically manage the fever, possibly using antipyretic medications. Third, if it is a bacterial infection, it is crucial to promptly administer a significant amount of effective antibiotics to treat it. Controlling the bacterial infection can prevent the progression of myasthenia gravis to a more severe state. (Note: Medication should be used under the guidance of a doctor.)

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Neurology
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What medicine should be taken for myasthenia gravis?

Myasthenia gravis is a type of neurological immunological disease in neurology, mainly caused by a disorder of the body's own immune function. Patients in the body will produce antibodies against acetylcholine receptors, thus affecting the transmission of nerve impulses at the neuromuscular junction. For this disease, the following medications are generally prescribed: The first type of medication is a cholinesterase inhibitor, which can increase the amount of acetylcholine at the neuromuscular junction, thereby effectively improving clinical symptoms. The second type of medication is corticosteroids, because this disease is caused by an abnormal inflammatory response. Therefore, taking corticosteroids can suppress the inflammatory response. Treatment generally starts with a small dose and gradually increases, maintaining for a period before gradually tapering off. It may also be necessary to take other immunosuppressants. (Please take the medication under the guidance of a doctor)

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What are the side effects of taking steroid medication for myasthenia gravis?

The side effects of steroids in treating myasthenia gravis mainly include Cushing's syndrome characterized by specific facial and bodily features, weight gain, swelling in the lower legs, purple striae, tendency to bleed easily, poor wound healing, acne, and menstrual disorders. There could also be ischemic necrosis of the femoral or humeral heads, osteoporosis and fractures, primarily compressive vertebral fractures, as well as pathological fractures of the long bones, muscle weakness, muscle atrophy, and hypokalemia syndrome. Gastrointestinal irritation is common, primarily nausea and vomiting, as well as peptic ulcers or perforation, pancreatitis, and suppressed growth in children.