Mucinous Cystadenoma: A Rare Hepatic Tumor in a Child

被引:5
|
作者
Ferraguti, Danielle A. [1 ]
McGetrick, Molly [2 ]
Zendejas, Ivan [3 ,4 ]
Hernandez-Gonzalo, David [5 ]
Gonzalez-Peralta, Regino [1 ]
机构
[1] Univ Florida, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Pediat, Gen Educ, Gainesville, FL USA
[3] Canyon Surg Associates, Div Hepatobiliary Surg, Intermt Med Ctr, Murray, UT USA
[4] Canyon Surg Associates, Div Surg, Intermt Med Ctr, Murray, UT USA
[5] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
来源
FRONTIERS IN PEDIATRICS | 2017年 / 5卷
关键词
liver mass; children; pediatrics; mucinous cystadenoma; liver tumors; HEPATOBILIARY CYSTADENOMA; BILIARY CYSTADENOMA; CYSTIC NEOPLASMS; LIVER; MANAGEMENT; STROMA;
D O I
10.3389/fped.2017.00215
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Mucinous cystadenomas (MCAs) of the liver (also called hepatic biliary cystadenomas) are rare tumors that comprise about 5% of cystic masses of the liver in adults. These slow-growing lesions most commonly occur in middle-aged individuals, with a female sex predominance. Herein, we present a MCA in a 6-year-old male, one of only very few such cases described in the pediatric literature to date. Although MCAs are generally considered benign lesions, malignant transformation rarely occurs. The recurrence rate is high when partial cyst excision is performed. Therefore, complete surgical cyst resection with clinical follow-up, including imaging, is warranted.
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页数:4
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