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射精系统囊肿:两例报告

Cysts of the ejaculatory system: a report of two cases.

作者信息

Yanai Toshihiro, Okazaki Tadaharu, Yamataka Atsuyuki, Urao Masahiko, Kobayashi Hiroyuki, Kato Yoshifumi, Lane Geoffrey J, Miyano Takeshi

机构信息

Department of Pediatric General and Urogenital Surgery, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

出版信息

Pediatr Surg Int. 2005 Nov;21(11):939-42. doi: 10.1007/s00383-005-1522-6.

Abstract

We report two cases of rare cystic dilatations of the ejaculatory system. In case 1, a 6-month-old boy was referred to us for the management of recurrent epididymo-orchitis (E-O) complicating open drainage and a colostomy was performed elsewhere for a purulent rectal discharge thought to be rectal duplication. Diagnostic imaging showed a retrovesical cyst. Urethrocystoscopy showed a swelling of the verumontanum. No fistula was seen between the cyst and rectum on colonoscopy. At laparotomy, both ejaculatory ducts and seminal vesicles were found to be fused into a mass with cystic dilatation of the ejaculatory duct. Intraoperative histopathology of the cyst identified a metaplastic epithelial lesion. The cyst was excised with bilateral vasoligation. Since surgery, 8 years ago, urination and defecation have been normal. In case 2, a 4-month-old boy presented with fever and a swollen right scrotum. Ultrasonography showed a retrovesical cyst. Right grade IV vesicoureteral reflux diagnosed on voiding cystourethrography was treated by ureter reimplantation (Cohen) but complicated by recurrent E-O. Urethrocystoscopy with retrograde contrast via the utriculus showed that the cyst opened on the verumontanum, that both ejaculatory ducts opened into the cyst, and there was reflux into the right vas deferens. Right vasoligation alone was performed through a scrotal approach. Although the cyst was not excised, there has been no recurrence of E-O nor enlargement of the cyst for 6 years. Cysts of the ejaculatory system should be considered in the etiology of recurrent E-O in prepubertal children and a high index of awareness is recommended.

摘要

我们报告两例射精系统罕见的囊性扩张病例。病例1,一名6个月大的男孩因复发性附睾炎(E - O)前来我院就诊,此前因脓性直肠排出物(被认为是直肠重复畸形)在其他地方进行了开放引流并实施了结肠造口术。诊断性影像学检查显示膀胱后囊肿。尿道膀胱镜检查显示精阜肿胀。结肠镜检查未发现囊肿与直肠之间存在瘘管。剖腹手术时发现双侧射精管和精囊融合成一个肿块,射精管呈囊性扩张。囊肿的术中组织病理学检查发现化生上皮病变。囊肿切除并进行了双侧输精管结扎。自8年前手术以来,排尿和排便一直正常。病例2,一名4个月大的男孩出现发热和右侧阴囊肿胀。超声检查显示膀胱后囊肿。排尿性膀胱尿道造影诊断为右侧IV级膀胱输尿管反流,通过输尿管再植术(科恩术式)进行治疗,但并发复发性附睾炎。经尿道膀胱镜检查并通过前列腺小囊进行逆行造影显示囊肿开口于精阜,双侧射精管均开口于囊肿,且有反流至右侧输精管。仅通过阴囊途径进行了右侧输精管结扎。尽管未切除囊肿,但6年来附睾炎未复发,囊肿也未增大。射精系统囊肿应被纳入青春期前儿童复发性附睾炎的病因考虑范围,建议高度警惕。

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