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Infantile disseminated visceral giant cell arteritis presenting as sudden infant death.

机译:婴儿弥散性内脏巨细胞动脉炎,表现为婴儿猝死。

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摘要

The rare clinicopathological entity 'disseminated visceral giant cell arteritis' (DVGCA) was first described in 1978. It is characterized by widespread small-vessel giant cell angitis and extravascular granulomas. A normal and healthy 7-month-old boy who presented unexpectedly with sudden infant death syndrome (SIDS) is reported. Histological examination at autopsy revealed giant cell angitis of the aorta, common carotid, coronary, pulmonary, celiac, mesenteric and common iliac arteries. There were also granulomas in the tracheal wall and liver. To our knowledge, this is the first documented case of DVGCA occurring in an infant younger than 12 months of age. A review of the literature on DVGCA is presented in this report, and the differential diagnosis is discussed.
机译:1978年首次描述了罕见的临床病理学实体“弥散性内脏巨细胞动脉炎”(DVGCA)。其特征是广泛存在的小血管巨细胞血管炎和血管外肉芽肿。据报道,一个正常健康的7个月大男孩意外出现婴儿猝死综合症(SIDS)。尸检的组织学检查显示主动脉,颈总动脉,冠状动脉,肺,腹腔,肠系膜和common总动脉有巨细胞性血管炎。气管壁和肝脏中也有肉芽肿。据我们所知,这是DVGCA的首例记录病例,发生于12个月以下的婴儿中。本报告介绍了有关DVGCA的文献,并讨论了鉴别诊断。

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