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副肝叶:儿童肝前性门静脉高压的罕见病因

Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child.

作者信息

Sağ Elif, Cansu Ayşegül, İmamoğlu Mustafa, Çakır Murat

机构信息

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.

Department of Radiology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.

出版信息

Pediatr Gastroenterol Hepatol Nutr. 2018 Oct;21(4):361-364. doi: 10.5223/pghn.2018.21.4.361. Epub 2018 Oct 10.

Abstract

Accessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable hepatosplenomegaly and portal hypertension. A diagnosis was made after taking an extensive medical history, observation and radiological examinations. The formal diagnosis was a prehepatic portal hypertension associated with accessory hepatic lobe.

摘要

副肝叶被视为儿童罕见疾病。根据其在患儿身上的位置、体积、类型和部位,可表现出各种症状和并发症。该患者为一名14个月大的女童,表现为明显的肝脾肿大和门静脉高压。在详细询问病史、进行观察和影像学检查后做出了诊断。正式诊断为与副肝叶相关的肝前门静脉高压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e20/6182474/694bc7df758d/pghn-21-361-g001.jpg

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