先天性肝囊肿。

IF 1.7 Q2 PEDIATRICS Clinical Medicine Insights-Pediatrics Pub Date : 2017-04-10 eCollection Date: 2017-01-01 DOI:10.1177/1179556517702853
Aldo Recinos, Tarik Zahouani, Juan Guillen, Benamanahalli Rajegowda
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引用次数: 10

摘要

先天性肝囊肿是一种罕见且无症状的婴儿和儿童疾病。其在产后生活中的发病率为2.5%,在产前的发病率要低得多。在产前影像学上偶然发现是最常见的表现。我们提出一个新生儿的情况下,胎儿超声检测到一个囊肿内的胎儿肝脏。出生后影像学显示肝右叶有肝囊肿,肝内其他结构未受影响。肝功能检查异常,但患者无症状。后路随访影像显示尺寸轻微减小。先天性肝囊肿的治疗通常是保守的,并定期进行超声监测。然而,当邻近结构发生水肿、进行性扩大、出血、扭转或压迫时,手术治疗是主要的治疗方法。可发生恶性转化,但极为罕见。部分或全部切除囊肿是有较大病变的新生儿的首选治疗方法。
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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Congenital Hepatic Cyst.

Congenital hepatic cyst is a rare and nonsymptomatic condition in infants and children. Its incidence is 2.5% in the postnatal life with a much lower incidence in the prenatal period. Incidental finding on antenatal imaging is the most common presentation. We present a case of a newborn in whom fetal ultrasound detected a cyst within the fetal liver. Postnatal imaging revealed a liver cyst in the right lobe of the liver, with no other intrahepatic structure affected. Liver function tests were abnormal, but the patient was asymptomatic. Posterior follow-up imaging showed a minor decrease in size. Management of congenital hepatic cyst is usually conservative, done with periodic ultrasound monitoring. However, surgical treatment is the mainstay of treatment when hydrops, progressive enlargement, hemorrhage, torsion, or compression of adjacent structures occurs. Malignant transformation can occur, but it is extremely rare. Partial or total removal of the cyst is the preferred treatment in neonates with a large lesion.

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