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Corrigendum: Operative experience on descending aorta with Takayasu arteritis: a review.
Front Cardiovasc Med
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Department of Vascular Surgery, Peking Union Medical College Hospital, Beijing, China.
[This corrects the article DOI: 10.3389/fcvm.2023.
View Article and Find Full Text PDFA rare presentation of pulmonary hypertension.
Int J Cardiol Congenit Heart Dis
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Department of Respiratory Medicine, University Hospital of Southampton, Tremona Rd, Southampton, SO16 6YD, United Kingdom.
[Clinical features and prognosis of children with multiple Takayasu's arteritis complicated with carotid artery occlusion].
Zhonghua Yu Fang Yi Xue Za Zhi
December 2024
Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing100020, China.
This study aimed to analyze the clinical characteristics and prognosis of Takayasu's arteritis (TA) with carotid artery occlusion in children. This study collected clinical data and follow-up information on the first diagnosis and treatment of c-TA combined with carotid artery occlusion in pediatric patients at the Children's Hospital affiliated with the Capital Institute of Pediatrics and Inner Mongolia Medical University Affiliated Hospital from 2013 to 2023. This study included four female patients with a mean age of (13.
View Article and Find Full Text PDFEfficacy of secukinumab in Takayasu arteritis with myocardial infarction complicated with generalized pustular psoriasis: A case report.
Medicine (Baltimore)
December 2024
Department of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Rationale: Takayasu arteritis (TAK) is an autoimmune disease that causes chronic inflammation targeting the aortic wall. Since many patients are resistant to steroid treatment, multiple immunosuppressants or interleukin-6 (IL-6) suppression therapy have served as treatment alternatives. However, there are very few reports on the effectiveness of biologics against inflammatory cytokines upstream of IL-6.
View Article and Find Full Text PDFTakayasu's arteritis in pregnancy: A case report and literature review.
Int J Gynaecol Obstet
December 2024
Department of Obstetrics and Gynaecology, Kathmandu Medical College Public Limited, Kathmandu, Nepal.
Article Synopsis
- * A case report describes a 23-year-old pregnant woman with TA who experienced fainting and arm pulselessness; she was diagnosed early, enabling timely treatment and comprehensive care.
- * Despite developing gestational hypertension and other complications, a successful emergency cesarean section at 36 weeks resulted in a healthy recovery for both mother and child, highlighting the importance of early diagnosis and collaborative medical care.
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