Suárez Aliago Begoña, Rodríguez Jiménez Inmaculada
Servicio de Radiodiagnóstico, MD Anderson, Madrid, España.
Arch Esp Urol. 2007 Nov;60(9):1.134-6.
We report a case of seminal vesicle cyst with ipsilateral renal agenesis associated wit abnormalities of the abdominal great vessels, not described previously in the bibliography.
33 year-old-male with history of abdominal pain and fever. This case was evaluated by ultrasound, IV urography, CT scan and MRI. RESULTS/CONCLUSIONS. Congenital cystic disease of the seminal vesicle is an uncommon disorder. It is associated with genitourinary anomalies, often renal agenesis, and even anomalies of the lower spine. However, anomalies of the abdominal great vessels have not been described previously. CT scan provided excellent demonstration of associated anomalies.
我们报告一例精囊囊肿合并同侧肾缺如，并伴有腹部大血管异常的病例，此前文献中未对此进行描述。
一名33岁男性，有腹痛和发热病史。该病例通过超声、静脉尿路造影、CT扫描和MRI进行评估。结果/结论：先天性精囊囊肿是一种罕见的疾病。它与泌尿生殖系统异常相关，常伴有肾缺如，甚至下脊柱异常。然而，此前尚未描述过腹部大血管异常。CT扫描能很好地显示相关异常。
