Nisar Muhammad Umar, Akhtar Nadeem, Gondal Mudassar Fiaz, Sikander Samer, Viqar Sana
Department of Paediatric Surgery, Children Hospital, PIMS, Islamabad, Pakistan.
PAEC General Hospital, Islamabad, Pakistan.
J Ayub Med Coll Abbottabad. 2018 Apr-Jun;30(2):275-277.
Aphallia or penile agenesis is very rare congenital anomaly of unknown cause occurring 1 in 30 million live births. Very little has been written in literature about aphallia. There is absent phallus and urethra may open abnormally in perineum or into rectum posing various surgical, social and psychological implications as the child grows. We are presenting 03 cases of aphallia with associated congenital anomalies such as unilateral renal agenesis, bilateral undescended testes, anorectal malformation and rectovasical fistula.
无阴茎或阴茎发育不全是一种非常罕见的先天性异常，病因不明，在每3000万活产中出现1例。关于无阴茎，文献中记载甚少。阴茎缺失，尿道可能在会阴异常开口或通向直肠，随着孩子成长会带来各种手术、社会和心理问题。我们现报告3例无阴茎合并先天性异常的病例，如单侧肾发育不全、双侧隐睾、肛门直肠畸形和直肠膀胱瘘。
