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高安动脉炎:并非血管成形术常见的病变。

Takayasu's aorto-arteritis: Not your regular lesion for angioplasty.

作者信息

Singh Navdeep, Athwani Vivek, Bansal Vikas, Kundra Shaveta

机构信息

Department of Pediatric Cardiology, SPS Hospitals, Ludhiana, Punjab, India.

Department of Pediatrics, SPS Hospitals, Ludhiana, Punjab, India.

出版信息

Ann Pediatr Cardiol. 2018 Sep-Dec;11(3):312-314. doi: 10.4103/apc.APC_28_18.

Abstract

We report a case of a 6-year-old female child with Takayasu's aorto-arteritis (TA) with severe coarctation of the aorta which resulted in an aortic dissection post-ballooning. This happened despite ensuring that markers for disease activity were negative, with appropriate corticosteroid therapy started before the procedure, and using a low-profile, low-pressure, and slightly undersized balloon for dilating the stenotic segment. It required immediate endovascular stenting to tide over the crisis. Following the procedure, she became normotensive with well-palpable lower limb pulses.

摘要

我们报告一例6岁女性儿童,患有高安动脉炎(TA)并伴有严重的主动脉缩窄,在球囊扩张术后发生了主动脉夹层。尽管确保疾病活动标志物为阴性,在手术前开始了适当的皮质类固醇治疗,并使用了低轮廓、低压且略小尺寸的球囊来扩张狭窄段,但仍发生了这种情况。这需要立即进行血管内支架置入以度过危机。手术后,她血压恢复正常,下肢脉搏可明显触及。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de81/6146849/69ab87cf53cd/APC-11-312-g001.jpg

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