Giant cell aortitis combined with arteritis and coarctation of the aorta in 3.5-month child: A case report and literature review

IF 2.3 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Yuliia Kuzyk, Dmytro Zerbino, Olga Kovalyk
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Abstract

A present case showing giant cell aortitis (GGA) with coarctation of the aorta can be considered unique, even after reviewing the literature. The case of a 3.5-month-old girl who suffered an acute viral infection with an increase in body temperature (up to 39.5°C), difficulty breathing, and diarrhea is described. The girl was diagnosed with nasopharyngitis, enterocolitis, meningoencephalitis; she died 20 hours after being hospitalized from multiple organ failure. Clinical and laboratory data were collected, and a pathological examination was performed. Histological examination of the aorta and its main branches, such as the brachiocephalic trunk, left common carotid artery, left subclavian artery, as well as internal organs, was performed using hematoxylin-eosin, Hart's resorcin-fuchsin, Weigert's picrofuchsin, and Masson's trichrome. Pathological examination revealed giant cell aortitis and arteritis with coarctation of the aorta. GCA, in our case, had pathomorphological signs. First, many plaques that protruded into the lumen of the aorta and main branches, such as the brachiocephalic trunk, left common carotid artery and left subclavian artery, had a conical end that resembled the appearance of a rash. Second, granulomatous inflammation was localized in the intima of the aorta and all layers of the above-mentioned arteries.
Our case of GCA in a 3.5-month-old girl is the youngest patient among those described. We first describe GCA in relation to other severe aortic diseases. Coarctation, in combination with an aneurysm of the ascending aorta and aortitis, is a pathology that has not yet been described.
3 个半月大的婴儿患巨细胞主动脉炎合并动脉炎和主动脉共动脉症:病例报告和文献综述。
本病例显示巨细胞性主动脉炎(GGA)伴有主动脉共动脉症,这在查阅文献后也被认为是独一无二的。本病例描述的是一名 3 个半月大的女童,因急性病毒感染导致体温升高(高达 39.5°C)、呼吸困难和腹泻。女童被诊断为鼻咽炎、小肠结肠炎和脑膜脑炎;住院 20 小时后死于多器官衰竭。收集了临床和实验室数据,并进行了病理检查。使用苏木精-伊红、Hart'sresorcin-fuchsin、Weigert's picrofuchsin和Masson's trichrome对主动脉及其主要分支(如肱脑干、左颈总动脉、左锁骨下动脉)以及内脏器官进行了组织学检查。病理检查显示,患者患有巨细胞主动脉炎和动脉炎,并伴有主动脉粥样硬化。在我们的病例中,GCA 具有病理形态学特征。首先,许多突入主动脉和主要分支(如肱动脉干、左颈总动脉和左锁骨下动脉)管腔的斑块末端呈圆锥形,外观类似皮疹。其次,肉芽肿性炎症位于主动脉内膜和上述动脉的各层。我们的病例是一名 3.5 个月大的女童,她的 GCA 是所描述病例中年龄最小的患者。我们首先介绍 GCA 与其他严重主动脉疾病的关系。主动脉粥样硬化合并升主动脉瘤和主动脉炎是一种尚未被描述过的病理现象。
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来源期刊
Cardiovascular Pathology
Cardiovascular Pathology 医学-病理学
CiteScore
7.50
自引率
2.70%
发文量
71
审稿时长
18 days
期刊介绍: Cardiovascular Pathology is a bimonthly journal that presents articles on topics covering the entire spectrum of cardiovascular disease. The Journal''s primary objective is to publish papers on disease-oriented morphology and pathogenesis from clinicians and scientists in the cardiovascular field. Subjects covered include cardiovascular biology, prosthetic devices, molecular biology and experimental models of cardiovascular disease.
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