Fetal mesenchymal hamartoma of the liver: A case report and literature review

被引:2
作者
Liu, Xin [1 ]
Tian, Sha [2 ]
Zhu, Zhenchuang [1 ]
Peng, Fei [1 ]
Yuan, Qiang [1 ]
Duan, Xufei [1 ]
Yan, Xueqiang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan Maternal & Child Healthcare Hosp, Dept Pediat Surg,Wuhan Childrens Hosp, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Wuhan Maternal & Child Healthcare Hosp, Tongji Med Coll, Dept Ultrasound,Wuhan Childrens Hosp, Wuhan, Peoples R China
关键词
mesenchymal hamartoma; liver tumor; fetus; prenatal examination; treat; 19Q MICRORNA CLUSTER; HEPATIC HAMARTOMA; DIAGNOSIS; MOSAICISM; DYSPLASIA; TUMORS; HEMANGIOENDOTHELIOMA; INFANT;
D O I
10.3389/fped.2022.1016260
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This paper reports the diagnosis and treatment process of a case of fetal mesenchymal hamartoma of the liver (MHL), and reviews the previous literature reports. At 38(+2) weeks of gestation, prenatal ultrasound found a well bound mixed solid and cystic mass, which was located at the lower edge of the right lobe of the liver and in front of the right kidney of the fetus, but the source and nature of the mass were not clear by ultrasound. Due to the approaching due date, the fetus showed no other abnormal symptoms, and no special treatment was given with the consent of the family members. A female fetus was delivered weighing 3,520 g at 39 weeks. An exploratory laparotomy was performed on the eighth day after delivery. During the operation, it was found that the tumor originated from the fifth, sixth and seventh hepatic segment and the corresponding hepatic segments were removed. Recovery was uneventful and the infant was discharged on the 6th day after surgery. Follow-up at 2 years showed a thriving young girl, and there was no tumor recurrence.
引用
收藏
页数:11
相关论文
共 45 条
[1]   Prenatal imaging of congenital hepatic tumors: a report of three cases [J].
Alamo, Leonor ;
Perrin, Ludovic ;
Vial, Yvan ;
Anooshiravani, Mehrak ;
Meuli, Reto .
CLINICAL IMAGING, 2017, 41 :112-117
[2]   Mesenchymal hamartoma of the liver: A case report [J].
Alwaidh, MH ;
Woodhall, CR ;
Carty, HT .
PEDIATRIC RADIOLOGY, 1997, 27 (03) :247-249
[3]   Mesenchymal Hamartoma of the Liver and DICER1 Syndrome [J].
Apellaniz-Ruiz, Maria ;
Segni, Maria ;
Kettwig, Matthias ;
Glueer, Sylvia ;
Pelletier, Dylan ;
Van-Hung Nguyen ;
Wagener, Rabea ;
Lopez, Cristina ;
Muchantef, Karl ;
Bouron-Dal Soglio, Dorothee ;
Sabbaghian, Nelly ;
Wu, Mona K. ;
Zannella, Stefano ;
Fabian, Marc R. ;
Siebert, Reiner ;
Menke, Jan ;
Priest, John R. ;
Foulkes, William D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (19) :1834-1842
[4]  
Arrunategui AM, 2017, J PEDIAT SURG CASE R, V21, P1, DOI 10.1016/j.epsc.2017.03.012
[5]   Concurrent infantile hemangioendothelioma and mesenchymal hamartoma in a developmentally arrested liver of an infant requiring hepatic transplantation [J].
Bejarano, PA ;
Serrano, MF ;
Casillas, J ;
Dehner, LP ;
Kat, T ;
Mittal, N ;
Rodriguez, MM ;
Tzakis, A .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2003, 6 (06) :552-557
[6]  
Bejvan SM, 1997, J ULTRAS MED, V16, P227
[7]  
Bessho T, 1996, PRENATAL DIAG, V16, P337, DOI 10.1002/(SICI)1097-0223(199604)16:4<337::AID-PD848>3.3.CO
[8]  
2-L
[9]   Mesenchymal hamartoma of the liver associated with features of Beckwith-Wiedemann Syndrome and high serum alpha-fetoprotein levels [J].
Cajaiba, Mariana M. ;
Sarita-Reyes, Carmen ;
Zambrano, Eduardo ;
Reyes-Mugica, Miguel .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2007, 10 (03) :233-238
[10]  
Cignini Pietro, 2007, J Prenat Med, V1, P45