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[精囊囊肿伴肾缺如]

[Seminal vesicle cyst with renal agenesis].

作者信息

López García J A, Azparren Echevarría J, Garmendia G, Madina J, Garmedia C, Hernández I, Arocena Lanz F

机构信息

Servicio de Urología, Hospital N.a Sra. de Aránzazu, San Sebastián, Guipúzcoa, España.

出版信息

Arch Esp Urol. 1998 Jun;51(5):419-26.

PMID:9675936
Abstract

OBJECTIVES

To describe 8 additional cases of seminal vesicle cyst associated with renal agenesis, an uncommon condition arising from anomalies occurring during embryonal development of the genitourinary system, and to analyze the utility of the different diagnostic imaging techniques.

METHODS

A retrospective study was conducted on 8 patients to determine the diagnostic possibilities of US (abdominal/transrectal), CT, MRI, urography, cystourethrography and cystoscopy. Transvesical percutaneous punction and deferentography, which permit diagnosis of blind-ending ureter, were utilized in two patients.

RESULTS

75% were left-sided and the age at presentation was generally between 25 to 45 years. The clinical features were related with irritative voiding symptoms, perineal discomfort and ejaculatory disorders. Treatment was based on the clinical features; 3 patients underwent resection via the abdominal retrovesical approach and 5 patients were treated conservatively.

CONCLUSIONS

Congenital seminal vesicle cyst may not be as uncommon as it is presumed to be and should be suspected in patients with solitary kidney and voiding disorders. The findings on pelvioabdominal US may suffice to suspect this condition. Although many diagnostic imaging techniques are available, blind-ending ureter can only be diagnosed by transvesical or transrectal percutaneous punction and deferentography. Treatment of symptomatic cases is by surgery, although conservative treatment is utilized more frequently.

摘要

目的

描述另外8例与肾缺如相关的精囊囊肿病例,这是一种由泌尿生殖系统胚胎发育异常引起的罕见病症,并分析不同诊断成像技术的效用。

方法

对8例患者进行回顾性研究,以确定超声(腹部/经直肠)、CT、MRI、尿路造影、膀胱尿道造影和膀胱镜检查的诊断可能性。两名患者采用经膀胱经皮穿刺和输精管造影术,以诊断盲端输尿管。

结果

75%为左侧,发病年龄一般在25至45岁之间。临床特征与刺激性排尿症状、会阴不适和射精障碍有关。治疗基于临床特征;3例患者通过腹部膀胱后入路进行切除,5例患者接受保守治疗。

结论

先天性精囊囊肿可能并不像人们认为的那样罕见,对于单肾和排尿障碍患者应怀疑此病。盆腔腹部超声检查结果可能足以怀疑此病。虽然有许多诊断成像技术可用,但盲端输尿管只能通过经膀胱或经直肠经皮穿刺和输精管造影术诊断。有症状病例的治疗方法是手术,尽管保守治疗更常用。

相似文献

1
[Seminal vesicle cyst with renal agenesis].[精囊囊肿伴肾缺如]
Arch Esp Urol. 1998 Jun;51(5):419-26.
2
[Seminal vesicle cyst and ipsilateral renal agenesis].
Arch Esp Urol. 2004 Mar;57(2):168-71.
3
[Seminal vesicle cyst associated with homolateral renal agenesis and megaureter. Apropos of a case].[精囊囊肿合并同侧肾缺如及巨输尿管。附1例报告]
Ann Urol (Paris). 1997;31(2):97-100.
4
[Diagnosis and treatment of seminal vesicle cyst].[精囊囊肿的诊断与治疗]
Zhonghua Wai Ke Za Zhi. 2003 Jun;41(6):433-5.
5
[Cyst of the seminal vesicle with ipsilateral kidney agenesis].精囊囊肿伴同侧肾缺如
Schweiz Med Wochenschr. 1991 Sep 14;121(37):1345-9.
6
Laparoscopic management of congenital seminal vesicle cysts associated with ipsilateral renal agenesis.
J Urol. 2002 Mar;167(3):1263-7.
7
[Congenital cysts of the seminal vesicles with ipsilateral kidney agenesis. Clinical aspects of 7 cases].[伴有同侧肾缺如的精囊先天性囊肿。7例临床情况]
Ann Urol (Paris). 1997;31(4):184-90.
8
Congenital seminal vesicle cyst associated with ipsilateral renal agenesis mimicking bladder outlet obstruction: a case report and review of the literature.先天性精囊囊肿伴同侧肾发育不全,模拟膀胱出口梗阻:病例报告及文献复习。
Kaohsiung J Med Sci. 2010 Jan;26(1):30-4. doi: 10.1016/S1607-551X(10)70005-X.
9
Ectopic ureter draining into seminal vesicle cyst: usefulness of MRI.异位输尿管引流至精囊囊肿:磁共振成像的作用
Radiat Med. 1998 Jul-Aug;16(4):309-11.
10
Renal agenesis associated with ipsilateral ectopic ureter entering a large seminal vesicle cyst.肾缺如伴同侧异位输尿管进入一个巨大的精囊囊肿。
Can J Urol. 2007 Feb;14(1):3463-6.