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Behcet's syndrome, as long as it is reasonable and effective** and there is no involvement of important organs, can be the same as the survival period of normal people. That is, it is perfectly capable of living for 20 years, 30 years or even longer.
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White. It's a syndrome, how long can you live, this really. There is no way to say that some will die after a short period of time, and some will live. Around 30 years old.
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Behcet's syndrome causes damage to many systems and organs in the body and needs to be treated with caution. At present, the disease can live for 20 to 30 years, depending on the severity of the patient's condition.
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The prognosis of most patients with Behcet's disease is very good and will not affect the life expectancy, that is, the age at which Behcet's disease lives is the same, which is mainly for those patients with local symptoms and no damage to important organs, and the prognosis of patients with Behcet's disease is relatively poor, such as the appearance of central nervous system lesions, its mortality rate is very high, and it is generally possible to die due to damage to some important organs one to two years after the onset of the disease. In addition, if there is a large arterial flow or myocardial infarction after the life of the large middle artery, it may lead to sudden aneurysm rupture, but this situation is very rare, and the prognosis of most patients is relatively good, but if the patient has ophthalmia, usually due to uveitis and retinal detachment, there is usually serious visual impairment left, and patients with Behcet's disease need to be actively carried out once ophthalmia and internal organs are involved** Corticosteroids and immunosuppressants are usually used to prevent the serious complications described above.
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It depends on the patient's condition.
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Patients with Behcet's syndrome can live for 30 or 50 years, or even longer, as long as they are diagnosed early and have a positive and effective **. Of course, some patients with ophthalmia often have visual impairment and even blindness, and if they are accompanied by important organ involvement, such as intestinal involvement or central nervous system involvement, it can also be life-threatening.
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As long as Behcet's disease is diagnosed early, it is reasonable and effective to be carried out at an early stage, and it is completely possible to live.
Seventy, eighty, or even longer.
Most patients with Behcet's disease survive for 10 years. Because Behcet's disease is often an alternating process of reversal and remission, the prognosis of most patients is good, while some patients often suffer from ophthalmia and are left with visual impairment, and some patients can have severe vision loss and even blindness.
However, in recent years, through the early active treatment of ophthalmia and the prevention of involvement of the unaffected eye, so that the blindness has been reduced, but there are still some patients who can have serious visual impairment, and a small number of patients have decreased survival rate because of damage to internal organs, such as gastrointestinal involvement, which can cause serious complications such as ulcers, bleeding, perforation, intestinal fistula, intestinal malabsorption, and infection of the gastrointestinal tract, and the mortality rate is very high, and the mortality rate of central nervous system lesions is also very high, although there are survivors, But there are often serious sequelae.
Patients with large and middle artery involvement may die suddenly due to ruptured aneurysm and myocardial infarction.
Patients with Behcet's syndrome have no problem as long as they are diagnosed early, and can live for 30 or 50 years, or even longer, after being actively and effectively**. Of course, some patients with ophthalmia often have visual impairment and even blindness, and if they are accompanied by important organ involvement, such as intestinal involvement or central nervous system involvement, it can also be life-threatening.
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