Prenatally Detected Congenital Perineal Mass Using 3D Ultrasound which was Diagnosed as Lipoblastoma Combined with Anorectal Malformation: Case Report

被引:12
作者
Ahn, Ki Hoon [1 ]
Boo, Yoon Jung [2 ]
Seol, Hyun Joo [1 ]
Park, Hyun Tae [1 ]
Hong, Soon Cheol [1 ]
Oh, Min Jeong [1 ]
Kim, Tak [1 ]
Kim, Hai Joong [1 ]
Kim, Young Tae [1 ]
Kim, Sun Haeng [1 ]
Lee, Kyu Wan [1 ]
机构
[1] Korea Univ, Coll Med, Dept Obstet & Gynecol, Dept Gen Surg, Seoul 136705, South Korea
[2] Korea Univ, Coll Med, Div Pediat Surg, Dept Gen Surg, Seoul 136705, South Korea
关键词
Perineum; Lipoblastoma; Prenatal Diagnosis; Congenital Abnormalities; Anal Canal; NEEDLE-ASPIRATION-CYTOLOGY; LIPOMATOUS TUMORS; LIPOSARCOMA; CHILDREN;
D O I
10.3346/jkms.2010.25.7.1093
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a case of prenatally diagnosed congenital perineal mass which was combined with anorectal malformation. The mass was successfully treated with posterior sagittal anorectoplasty postnatally. On ultrasound examination at a gestational age of 23 weeks the fetal perineal mass were found on the right side. Any other defects were not visible on ultrasonography during whole gestation. Amniocentesis was performed to evaluate the fetal karyotyping and acetylcholinesterase which were also normal. As the fetus grew up, the mass size was slowly increased more and more. At birth, a female neonate had a perineal mass on the right side as expected. During operation, the anal sphincteric displacement was found near the mass and reconstructed through posterior sagittal incision. This is the first reported case of prenatally diagnosed congenital perineal mass, after birth which was diagnosed as lipoblastoma and even combined with anorectal malformation. This case shows that it can be of clinical importance to be aware of this rare fetal perineal mass in prenatal diagnosis and counseling.
引用
收藏
页码:1093 / 1096
页数:4
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