一名患有系统性红斑狼疮的青少年主动脉瘤破裂。

IF 0.7 4区 医学 Q4 PEDIATRICS
Laura M Pérez, Marianela Fiorotto, Giselle Villarreal, María M Katsicas, Pedro Rino
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性、多系统、自身免疫性疾病。该病常累及心血管,但动脉瘤和/或主动脉夹层是罕见的致命并发症。本文旨在描述系统性红斑狼疮在儿科的一种罕见致命并发症,并回顾相关文献。我们介绍了一例 16 岁女孩的病例,她患有系统性红斑狼疮,多系统受累,确诊时无心血管疾病。她因剧烈胸痛就诊。胸部X光片显示主动脉弓扩张,无心脏肿大。怀疑存在夹层,于是进行了血管造影。确诊为降主动脉瘤,但没有夹层瓣。患者开始接受降压治疗。做完瓦尔萨尔瓦动作后,她出现动脉瘤破裂。入院 12 小时后死亡。动脉瘤和夹层是小儿系统性红斑狼疮中不常见的并发症。由于这两种并发症的死亡率很高,因此在系统性红斑狼疮患者出现胸痛时必须考虑这两种并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ruptured aortic aneurysm in an adolescent with systemic lupus erythematosus.

Systemic lupus erythematosus (SLE) is a chronic, multisystem, autoimmune disease. Cardiovascular involvement is frequent; however, aneurysm and/or aortic dissection are rare entities with fatal evolution. The objective is to describe a rare and fatal complication of SLE in pediatrics and review the literature. We present the case of a 16-year-old girl with SLE with multisystem involvement without cardiovascular disease at diagnosis. She consulted for severe chest pain. Chest X-ray showed a dilated aortic arch with no cardiomegaly. The presence of a dissection was suspected, and an angiotomography was performed. A descending aortic aneurysm without a dissection flap was confirmed. Antihypertensive treatment was started. After a Valsalva maneuver, she presented an aneurysmal rupture. She died 12 hours after admission. Aneurysm and dissection are infrequent complications in pediatric SLE. As they have high mortality, it is essential to consider them in a patient with SLE and chest pain.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
286
审稿时长
6-12 weeks
期刊介绍: Archivos Argentinos de Pediatría is the official publication of the Sociedad Argentina de Pediatría (SAP) and has been published without interruption since 1930. Its publication is bimonthly. Archivos Argentinos de Pediatría publishes articles related to perinatal, child and adolescent health and other relevant disciplines for the medical profession.
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