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由于巨型肝囊引起的肠道阻塞:一个病例报告

Adem Küçük¹, Shukri Said Mohamed², Abdishakur Mohamed Abdi²

¹Düzce University Faculty of Medicine, Pediatric Surgery Clinic, Düzce 81110, Merkez, Turkey. ademkucuk81@hotmail.com.

World journal of clinical cases

|September 21, 2023

概括

先天性肝囊虽然很少见,但会变得巨大的,并引起严重的症状. 手术化为婴儿的这些大型简单肝囊提供了成功的治疗方法.

科学领域:

儿科手术儿科手术
肝胆道医学肝胆道医学
医疗成像医学成像

背景情况:

先天性肝囊是罕见的,但越来越多的产前诊断.
它们根据胆汁连接被分类为简单或肝内胆囊.
虽然在成年人中往往是偶然的,但在婴儿中可能是有症状的,出现吐或呼吸问题.

研究的目的:

报告一个婴儿患有巨型先天性肝囊的病例.
为突出这种罕见的儿科病例的诊断和管理方法.

主要方法:

一个3个月大的婴儿出现吐,呼吸困难和腹部膨胀.
诊断成像包括超声波和磁共振成像,揭示了一个大的囊性病变.
患者在稳定后接受了外科窗.

主要成果:

图像检测证实了一个单独的囊性病变,尺寸为10厘米×10厘米×14厘米,延伸到骨盆.
手术后的康复是成功的,口服营养开始于第二天,排水在第五天.
在1个月的随访期内,婴儿没有任何临床投诉.

结论:

先天性肝囊通常是良性的,但很少会生长到巨大的尺寸.
巨型囊可能导致严重的并发症,如呼吸困难和肠道阻塞.
手术化是巨型简单肝囊的有效治疗方法,取得了成功的结果.

关键词:

案例报告案例报告先天性肝脏囊是一种先天性肝脏囊.窗户装饰窗户装饰窗户装饰肠道阻塞肠道阻塞疼痛疼痛疼痛疼痛一个简单的肝脏囊

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