{"id":13133,"date":"2024-08-23T04:41:15","date_gmt":"2024-08-23T02:41:15","guid":{"rendered":"https:\/\/valintermed.com\/?p=13133"},"modified":"2024-08-23T04:41:15","modified_gmt":"2024-08-23T02:41:15","slug":"arteriit-takayasu","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/arteriit-takayasu\/","title":{"rendered":"Takayasu's arteritis"},"content":{"rendered":"
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Takayasu's arteritis is a rare systemic inflammatory disease that affects large vessels, primarily the aorta and its major branches. This disease is an example of vascular hyacinth and can lead to serious circulatory disorders. It is mainly observed in young women aged 15 to 40 years. The etiopathogenesis of Takayasu's arteritis is not fully understood, but it is assumed that it is caused by immunological mechanisms and may have an autoimmune nature. The clinical picture is varied, including such manifestations as fatigue, fever, weight loss, as well as specific symptoms related to vascular damage, such as organ dysfunction caused by stenosis or occlusion of arteries.<\/p>\n

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