阴茎缺如
Agenesis of penis.
作者信息
Pal Diya, Pal Dilip Kumar
机构信息
Department of Surgery, MGM Medical College, Kishanganj, Bihar, West Bengal, India.
Department of Urology, Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
出版信息
Urol Ann. 2020 Oct-Dec;12(4):379-381. doi: 10.4103/UA.UA_29_20. Epub 2020 Oct 15.
Abstract
Agenesis of penis is a very rare developmental anomaly, which is usually associated with scrotal hypoplasia or other urological developmental anomalies. Here we psesent such a case who presented to us with stenosis of newly constructed urethra.
摘要
阴茎缺如为一种极为罕见的发育异常，通常与阴囊发育不全或其他泌尿系统发育异常相关。在此我们报告这样一例因新建尿道狭窄前来就诊的病例。 （注：原文中“psesent”拼写错误，应为“present”）
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本文引用的文献
1
Congenital absence of the penis; a report of a case with congenital concealed penile agenesis and congenital absence of the left kidney and ureter.
J Urol. 1961 Sep;86:343-5. doi: 10.1016/S0022-5347(17)65174-7.
2
Should infants with aphallia be raised as females?
Indian Pediatr. 2003 Aug;40(8):802-3; author reply 803.
3
Aphallia.
Indian Pediatr. 2003 Apr;40(4):367-8.
4
Male gender assignment in penile agenesis: a case report and review of the literature.阴茎发育不全的男性性别认定：一例病例报告及文献综述
J Pediatr Surg. 1995 Sep;30(9):1358-60. doi: 10.1016/0022-3468(95)90505-7.
5
Testicular function in 2 cases of penile agenesis.
J Urol. 1981 Oct;126(4):556-7. doi: 10.1016/s0022-5347(17)54625-x.
6
Penile agenesis.阴茎发育不全
J Urol. 1972 Sep;108(3):496-9. doi: 10.1016/s0022-5347(17)60785-7.
7
Agenesis of penis. Embryology and management.阴茎缺如。胚胎学与处理
Urology. 1973 Mar;1(3):226-9. doi: 10.1016/0090-4295(73)90741-3.
8
Penile agenesis: a report of six cases.
J Pediatr Surg. 1987 Feb;22(2):172-4. doi: 10.1016/s0022-3468(87)80441-4.
9
Aphallia: its classification and management.无睾症：其分类与处理
J Urol. 1989 Mar;141(3):589-92. doi: 10.1016/s0022-5347(17)40903-7.
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