胎儿巨大尿路瘤第二次“弹出”:1例报告及复习。

IF 2.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY BMC Pregnancy and Childbirth Pub Date : 2025-02-17 DOI:10.1186/s12884-025-07279-8
Xiaoying Qi, Houqing Pang, Ling Wang, Yifei Tan, Hong Luo
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摘要

背景:胎儿肾穹穹破裂伴尿液瘤形成是一种罕见的情况,它作为一种“爆裂”机制来缓冲肾盂压力。肾盂输尿管交界处梗阻(UPJO)是产前肾盂积水最常见的原因,但很少导致尿瘤的形成。胎儿尿瘤可能预示着出生后肾功能不佳。我们报告一个罕见的病例upjo相关的尿瘤伴尿腹水,破裂在阴道分娩。病例介绍:一名30岁妇女在妊娠25+3周因胎儿双侧肾积水入院。这个可能的UPJO病例在29+5周时变得更加复杂,左肾周围出现尿瘤和腹水。随后尿瘤逐渐增大,腹水加重,并伴有睾丸鞘膜积液、胸腔积液、羊水过多。36+1周最后一次产前超声显示尿瘤大小约为9.0 × 6.3 × 8.7 cm。羊膜过早破裂,男婴在37周顺产。婴儿腹胀逐渐加重。床边超声显示尿瘤不规则变小,伴有腹水明显增多。据推测,尿瘤可能会发生二次破裂。行腹水引流,尿瘤消失。但2天后再次出现,血清肌酐显著升高。父母选择放弃治疗。令人惊讶的是,婴儿出院后的喂养和心理健康状况良好。3个月时血清肌酐恢复正常。由于巨大的尿瘤压迫周围组织,婴儿在6个月时接受了尿瘤切除术。到一岁时,婴儿发育正常,没有肾脏损伤的迹象。结论:产前鉴别大型尿路瘤合并尿腹水需要给予必要的重视和适当的处理策略。产前尿瘤引流适用于有难产或分娩破裂风险的大尿瘤。产后腹水需要主动引流,以防止肌酐和尿素重吸收及其他并发症。小的无症状尿瘤可以保守治疗,但对于大的或复发的对周围组织有压力的尿瘤,建议早期手术治疗。
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Second 'pop-off' of fetal giant urinoma: case report and review.

Background: Renal fornices rupture with urinoma formation in fetuses is an unusual condition that acts as a 'pop off' mechanism to buffer renal pelvis pressure. Ureteropelvic junction obstruction (UPJO) is the most common cause of prenatal hydronephrosis, but it rarely leads to the formation of urinoma. Fetal urinoma could be indicative of poor renal function after birth. We report a rare case of UPJO-related urinoma accompanied with urinary ascites, which ruptured during vaginal delivery.

Case presentation: A 30-year-old woman was admitted to our hospital at 25+3 weeks gestation for fetal bilateral hydronephrosis. This probable case of UPJO became further complicated at 29+5 weeks with the presence of a urinoma around the left kidney and ascites. Afterwards, the urinoma gradually enlarged and the ascites worsened, accompanied by testicular hydrocele, pleural effusion, and polyhydramnios. The last prenatal ultrasound at 36+1 weeks disclosed that the size of the urinoma was approximately 9.0 × 6.3x8.7 cm. The amniotic membrane ruptured prematurely and a male infant was vaginally delivered at 37 weeks. The baby developed gradually worsening abdominal distension. Bedside US revealed the urinoma became irregular and smaller, accompanied by a significant increase in ascites. It was speculated that the urinoma might experience a secondary rupture. Ascites drainage was performed and the urinoma disappeared. But it reemerged 2 days later with a significant increase in serum creatinine. The parents opted to abandon treatment. Surprisingly, the infant developed good feeding and mental health after discharge. Serum creatinine returned to normal at 3 months. Due to compression of surrounding tissues by the huge urinoma, the infant accepted urinoma resection surgery at 6 months. By the age of one, the infant was developing normally without signs of renal impairment.

Conclusions: Prenatal identification of a large urinoma with urinary ascites requires necessary attention and appropriate management strategies. Prenatal urinoma drainage is indicated for large urinoma risking dystocia or rupture during delivery. Postnatal ascites requires active drainage to prevent creatinine and urea reabsorption and other complications. Small asymptomatic urinoma can be managed conservatively, but early surgery is recommended for large or recurrent urinoma exerting pressure on surrounding tissues.

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来源期刊
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth OBSTETRICS & GYNECOLOGY-
CiteScore
4.90
自引率
6.50%
发文量
845
审稿时长
3-8 weeks
期刊介绍: BMC Pregnancy & Childbirth is an open access, peer-reviewed journal that considers articles on all aspects of pregnancy and childbirth. The journal welcomes submissions on the biomedical aspects of pregnancy, breastfeeding, labor, maternal health, maternity care, trends and sociological aspects of pregnancy and childbirth.
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