婴儿左侧胆囊和奇莱蒂综合征。

JPGN reports Pub Date : 2024-12-16 eCollection Date: 2025-02-01 DOI:10.1002/jpr3.12153
Laura J Bradstreet, Teresa Chapman, Jonathan O Swanson, Katryn N Furuya
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引用次数: 0

摘要

先天性肝脏异常可能与重要的肠道异常、血管异常有关,也可能是无症状的偶然发现的。不常见和罕见的解剖性肝脏和胆道疾病包括左侧胆囊、游离肝、肝脏旋转不良和肝-膈肠介入(Chilaiditi综合征)。本报告描述了一个偶然发现胆囊错位到左肝叶上表面的婴儿,并伴有Chilaiditi综合征,一种未在文献中描述的配置。讨论了管理方面的考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Left-sided gallbladder and Chilaiditi syndrome in an infant.

Congenital hepatic anomalies may be associated with important intestinal abnormalities, vascular anomalies, or may be asymptomatic and discovered incidentally. Uncommon and rare anatomic liver and biliary disorders include left-sided gallbladder, wandering liver, malrotation of the liver, and hepato-diaphragmatic interposition of the bowel (Chilaiditi syndrome). This report describes an infant with incidentally discovered malpositioning of the gallbladder to the superior surface of the left hepatic lobe, coupled with Chilaiditi syndrome, a configuration that has not been described in the literature. Management considerations are discussed.

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