Suppr超能文献

川崎病累及神经系统和心血管系统:一例病例报告及文献综述

Kawasaki disease involving both the nervous system and cardiovascular system: a case report and literature review.

作者信息

Yin Wen, Wu Yali, Wang Shasha, Tang Hongxia, Ding Yan

机构信息

Department of Rheumatology and Immunology, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China.

出版信息

Front Pediatr. 2024 Dec 2;12:1459143. doi: 10.3389/fped.2024.1459143. eCollection 2024.

Abstract

BACKGROUND

Kawasaki disease (KD), an acute self-limiting vasculitis, is the main cause of acquired heart disease. Timely diagnosis and treatment can mitigate the occurrence of complications and improve patient prognosis. Facial nerve paralysis (FNP) and ptosis are rare complications of KD and are rarely reported, but FNP is considered a high risk factor for coronary aneurysms. If giant coronary artery aneurysms are formed, clinicians should be vigilant when diagnosing the formation of systemic artery aneurysms (SAAs).

PATIENT PRESENTATION

A 10-month-old girl with fever, diffuse rash, and conjunctival congestion was hospitalized locally, diagnosed with KD, and treated with intravenous infusion of gamma globulin (IVIG). She had fever again after 1 week of temperature stability, accompanied by conjunctival congestion, and was treated with a second dose of IVIG, but she still experienced recurrent fever. The day prior to admission, she developed facial asymmetry, left FNP, diffuse erythema and membranous peeling of the fingers of both hands. The patient's body temperature normalized after treatment with 20 mg/kg methylprednisolone, but cardiac ultrasound revealed progressive enlargement of the coronary artery aneurysms. On day 37of the illness, transient eyelid ptosis developed; fortunately, the left FNP and eyelid ptosis finally resolved, leaving no sequelae. Two years and eight months after onset, the patient developed bilateral humeral aneurysm.

CONCLUSION

This is the first KD patient involving two neurological complications combined with giant coronary artery aneurysms and SAAs. KD needs to be considered in infants with unexplained recurrent fever who present with FNP or ptosis. FNP secondary to KD is a high risk factor for coronary artery aneurysms, so it is necessary to perform cardiac ultrasound for accurate diagnosis. KDs combined with giant coronary aneurysms require careful physical examination and noninvasive angiography during follow-up to detect SAA formation.

摘要

背景

川崎病(KD)是一种急性自限性血管炎,是后天性心脏病的主要病因。及时诊断和治疗可减轻并发症的发生并改善患者预后。面神经麻痹(FNP)和上睑下垂是KD罕见的并发症,鲜有报道,但FNP被认为是冠状动脉瘤的高危因素。若形成巨大冠状动脉瘤,临床医生在诊断系统性动脉动脉瘤(SAA)形成时应保持警惕。

病例介绍

一名10个月大的女童,因发热、弥漫性皮疹和结膜充血在当地住院,诊断为KD,并接受静脉输注丙种球蛋白(IVIG)治疗。体温稳定1周后再次发热,伴有结膜充血,接受第二剂IVIG治疗,但仍反复发热。入院前一天,出现面部不对称、左侧FNP、双手手指弥漫性红斑和膜状脱皮。用20 mg/kg甲泼尼龙治疗后患者体温恢复正常,但心脏超声显示冠状动脉瘤逐渐增大。病程第37天出现短暂性眼睑下垂;幸运的是,左侧FNP和眼睑下垂最终消退,未留后遗症。发病两年零八个月后,患者出现双侧肱骨动脉瘤。

结论

这是首例涉及两种神经系统并发症并合并巨大冠状动脉瘤和SAA的KD患者。对于出现FNP或上睑下垂且原因不明反复发热的婴儿,需考虑KD。KD继发的FNP是冠状动脉瘤的高危因素,因此有必要进行心脏超声以准确诊断。合并巨大冠状动脉瘤的KD患者在随访期间需要仔细的体格检查和无创血管造影以检测SAA的形成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验