Prenatal Diagnosis of True Diphallia and Associated Anomalies

被引:4
|
作者
Tu, Yi-An
Su, Yi-Ning
Yang, Po-Kai
Shih, Jin-Chung [1 ,2 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Obstet & Gynecol, 15F,8,Chung Shan South Rd, Taipei 10002, Taiwan
[2] Natl Taiwan Univ, Coll Med, Taipei 10002, Taiwan
来源
OBSTETRICS AND GYNECOLOGY | 2014年 / 124卷 / 02期
关键词
D O I
10.1097/AOG.0000000000000327
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Diphallia poses several surgical, psychological, and esthetic issues. Currently, diphallia is only diagnosed after birth. CASE: We present a true diphallia in one fetus of dichorionic twins noted at 23 weeks of gestation. In this fetus, two phallus-like protrusions and a bifid scrotum, as well as a duplicated collecting system of both kidneys, were found on ultrasonogram. Unfortunately, the fetus died near term. CONCLUSION: Diphallia, although exceedingly rare, can be precisely diagnosed antenatally. Careful ultrasound examination of the origins of the fetal phallus and of other adjacent organs is essential to establish the diagnosis of diphallia and to detect any associated anomalies.
引用
收藏
页码:416 / 418
页数:3
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