Departments of Gynecology-Obstetrics, Hôpital Mère-Enfant, CHU de Nantes, Nantes, France.
Fetal Diagn Ther. 2011;30(3):239-40. doi: 10.1159/000331447. Epub 2011 Sep 17.
Cloacal anomaly is a rare malformation with an incidence of 1 in 50,000 births. The definitive prenatal diagnosis of cloacal dysgenesis sequence is difficult. The use of three-dimensional (3-D) ultrasonography helps to describe the perineum and change diagnosis. In our case report, a large median genital structure was visualized, which was initially considered a penis-like structure, but the 3-D technique showed an enlarged bud. The urethral meatus was at the tip of this smooth structure. The lack of anal structure was clearly demonstrated.
直肠肛门畸形是一种罕见的畸形,发病率为每 5 万出生婴儿中有 1 例。直肠肛门发育不良序列的明确产前诊断较为困难。三维(3-D)超声的应用有助于描述会阴并改变诊断。在我们的病例报告中,可见一个大的中间生殖器结构,最初被认为是阴茎样结构,但 3-D 技术显示为一个增大的芽。尿道口位于这个光滑结构的顶端。明显没有肛门结构。