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首页> 外文期刊>Journal of Korean medical science >Prenatally detected congenital perineal mass using 3D ultrasound which was diagnosed as lipoblastoma combined with anorectal malformation: case report.
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Prenatally detected congenital perineal mass using 3D ultrasound which was diagnosed as lipoblastoma combined with anorectal malformation: case report.

机译:使用3D超声在产前检测到的先天性会阴部肿块,被诊断为脂肪母细胞瘤合并肛门直肠畸形:病例报告。

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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.
机译:我们报告一例产前诊断为先天性会阴部肿块,并合并肛门直肠畸形。产后成功进行了后矢状肛门直肠成形术治疗。在23周胎龄的超声检查中,右侧发现胎儿会阴部肿块。整个妊娠期间,其他任何缺陷在超声检查中均不可见。进行羊膜穿刺术以评估同样正常的胎儿核型和乙酰胆碱酯酶。随着胎儿的成长,肿块的大小逐渐增加。出生时,一名女性新生儿的右侧会阴部肿块符合预期。手术期间,在肿块附近发现肛门括约肌移位,并通过后矢状切口切开。这是第一例报道的产前诊断为先天性会阴肿块,出生后被诊断为脂肪母细胞瘤,甚至合并肛门直肠畸形。该病例表明,在产前诊断和咨询中意识到这种罕见的胎儿会阴部肿块可能具有临床意义。

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