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.

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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

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Короткий адрес: https://sciup.org/14121590

IDR: 14121590   |   DOI: 10.33619/2414-2948/73/17

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