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.
机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USA
Dean, GE
Shah, SK
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USA
机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USA
Dean, GE
Shah, SK
论文数: 0引用数: 0
h-index: 0
机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Urol, Camden, NJ 08103 USA