Clinical case in Takayasu artery with critical lesion in aortic arch branches (Takayasu's disease)
Автор: Zhumaeva Khadija, Uraimov Omurbek, Zhanbaeva Anara, Imetova Zhazgul, Abdullaeva Zhypargul
Журнал: Бюллетень науки и практики @bulletennauki
Рубрика: Медицинские науки
Статья в выпуске: 12 т.7, 2021 года.
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Research relevance: among Kyrgyz patients with Takayasu arteritis (AT), young women were predominated. The etiology is unknown. Research objectives: observation of the clinical manifestations in Takayasu’s arteritis in patients with the aim of compiling a diagnosis in treatment of disease. Research methods: most of patients had anatomical type V Takayasu arteritis (61.3%), vascular stage (89.3%) and severe stenosis (54.7%), lesions of the brachiocephalic trunk (68%), common sleepyheads (57.3%) and renal (52%) arteries. Severe exacerbation of the disease was observed in 82.7% of patients. The presence of ≥2 complications worsened the prognosis of AT. Research results: the clinical manifestations of AT were characterized mainly by cardiovascular pathology (77.3%) and kidney damage (57.3%). Conclusions: more than one third of patients (37.3%) had late diagnosis of AT.
Nonspecific aortoarteritis, syndrome or takayasu disease, aortoarteritis obliterans, general inflammatory reaction syndrome, stenosis of the aorta and its branches, absence of pulse, asymmetry of blood pressure, circulatory failure, cerebral ischemia
Короткий адрес: https://sciup.org/14121590
IDR: 14121590 | DOI: 10.33619/2414-2948/73/17