Persistent Mullerian Duct Syndrome With Torsion of a Transverse Testicular Ectopia: First Reported Case

被引:7
作者
Chaabane, Wassim [1 ]
Jarboui, Lamia
Sahnoun, Ahmed
Daoud, Emna
Hadjsliman, Mourad
Fakhfekh, Hammadi
Bahloul, Ali
Mhiri, Mohamed Nabil
机构
[1] Habib Bourguiba Univ Hosp Ctr, Dept Urol, Sfax 3000, Tunisia
关键词
D O I
10.1016/j.urology.2009.10.021
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Persistent Mullerian duct syndrome with transverse testicular ectopia is a rare pathologic association. A 7-month-old boy was admitted to the emergency department with a right testicular swelling. Physical examination revealed a tender right testis, the upper limits of which could not be palpated. The left testis was impalpable. An ultrasound revealed a normal right testis with an evident blood flow, overcome by a similar mass but avascular. At surgery, the right hernial sac contained both testes with an infantile uterus and fallopian tubes. The left testis was viable after manipulation. Proximal-salpingectomy with corporeal hysterectomy was performed to allow bilateral scrotal orchiopexy. UROLOGY 76: 65-66, 2010. (C) 2010 Elsevier Inc.
引用
收藏
页码:65 / 66
页数:2
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