Abnormal urethral pathways in a child presenting with diphallia

被引：2

作者：

Kendrick, Dylan John ^{[1
]}

Goddard, Lucy Erin ^{[2
]}

Kimble, Roy Mark ^{[1
,2
,3
]}

机构：

[1] Univ Queensland, Sch Med, Brisbane, Qld, Australia

[2] Queensland Childrens Hosp, 501 Stanley St, South Brisbane, Qld 4101, Australia

[3] Queensland Univ Technol, Sch Hlth Sci, Brisbane, Qld, Australia

来源：

JOURNAL OF PEDIATRIC SURGERY CASE REPORTS | 2021年 / 66卷

关键词：

Diphallia; Duplicate penis; Urethral duplication; Congenital anomaly;

D O I：

10.1016/j.epsc.2021.101802

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Diphallia is an extremely rare embryological anomaly, occurring once in 5-6 million births. Here we discuss a neonate who was referred for surgical consultation of diphallia, in which examination revealed a dominant right phallus and apparently shorter left phallus. MRI and retrograde urethrogram revealed a unique pathway of the right urethra and a stenosed, but otherwise normal left urethra. The decision was made to excise the right phallus and associated urethra due to the correct anatomy of the left phallus and corresponding urethra.

引用

页数：3