Shibui Yuichi, Obata Satoshi, Hirose Ryuichiro, Nakano Ryo, Setoue Takashi, Miyazaki Takeshi, Matsuoka Hirofumi, Sato Toshihiko
Department of General Thoracic, Breast, and Pediatric Surgery, Fukuoka University, 7-45-1, Nanakuma Jonan-Ku, Fukuoka, Fukuoka, 814-0180, Japan.
Department of Pediatric Surgery, Faculty of Medicine, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.
Surg Case Rep. 2023 Oct 31;9(1):191. doi: 10.1186/s40792-023-01772-y.
Sacrococcygeal teratomas (SCTs) are known to cause urological complications, but urethrovaginal (UV) fistula as a complication of SCT is rare. We herein report a case of SCT with UV fistula and hydrocolpos.
A 1-day-old female neonate presented to our department with prominent swelling in the sacrococcygeal region. She was born at 37 gestational weeks via spontaneous vaginal delivery from a 39-year-old woman. The weight of the baby was 2965 g, and her Apgar scores were 4/10 (at 1 and 5 min). An MRI examination confirmed an 11 × 11 cm Altman classification typeII SCT associated with hydrocolpos, a dilated urinary bladder, and bilateral hydronephrosis. When she was 5 days, the SCT was excised totally and a coccygectomy was performed. After the operation, as her urinary output appeared unstable, a cystoscopic examination was performed on the third postoperative day. This revealed that the UV fistula was located approximately 1 cm from the urethral opening. In addition, the proximal urethra was unobstructed and connected to the bladder. The cystoscope allowed for the passage of a urinary catheter through the urethra. After 1 month of catheter placement, she was discharged from the hospital at 57 days of age. Follow-up was uneventful, with neither urinary infection nor retention.
SCTs are associated with not only trouble with rectal function and lower extremity movement but also urinary complications. The pathogenesis of this UV fistula is thought to be the rapid growth of the SCT that developed in the fetal period, resulting in obstruction of the urethra by the tumor and the pubic bone, which in turn caused urinary retention and the formation of a fistula as an escape route for the pressure. Because SCTs can cause a variety of complications depending on the course of the disease, careful examination and follow-up are necessary.
骶尾部畸胎瘤(SCTs)已知会引起泌尿系统并发症,但尿道阴道(UV)瘘作为SCT的一种并发症较为罕见。我们在此报告一例伴有UV瘘和阴道积水的SCT病例。
一名1日龄女婴因骶尾部明显肿胀入住我科。她是通过自然阴道分娩出生的,孕周37周,母亲为39岁女性。婴儿体重2965克,阿氏评分在1分钟和5分钟时分别为4/10。MRI检查证实为一个11×11厘米的阿尔特曼分类II型SCT,伴有阴道积水、膀胱扩张和双侧肾积水。在她5天时,对SCT进行了全切并实施了尾骨切除术。术后,由于她的尿量似乎不稳定,在术后第三天进行了膀胱镜检查。结果显示UV瘘位于距尿道口约1厘米处。此外,尿道近端通畅并与膀胱相连。膀胱镜能够使导尿管通过尿道。放置导尿管1个月后,她在57日龄时出院。随访期间情况良好,既无泌尿系统感染也无尿潴留。
SCTs不仅与直肠功能和下肢运动问题有关,还与泌尿系统并发症有关。这种UV瘘的发病机制被认为是胎儿期发育的SCT快速生长,导致肿瘤和耻骨压迫尿道,进而引起尿潴留,并形成瘘管作为压力的释放途径。由于SCTs会根据疾病进程引发各种并发症,因此仔细的检查和随访是必要的。