Ureteroinguinal Herniation with Consecutive Ureteral Stricture in a 2-Month-Old Infant: Case Report.

Pub Date : 2024-01-22 eCollection Date: 2024-01-01 DOI:10.1055/s-0044-1779253
Carlos Delgado-Miguel, Antonio Jesus Muñoz-Serrano, Pablo Aguado, Ennio Fuentes, Ricardo Díez
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Abstract

Inguinal herniation of ureter is an uncommon finding among children, with scarce reported cases in the literature to date, that can potentially lead to obstructive uropathy. We report a case of ureteroinguinal herniation discovered during an inguinal hernia repair in a patient with antenatally ultrasound finding of hydronephrosis. A 2-month-old infant with antenatal left hydronephrosis presented with left inguinal mass. Preoperative ultrasound showed an anechoic tubular image producing a mass effect on the left testicle, with suspected bladder herniation and/or dilated ureter toward the inguinal canal. An open surgical inguinal exploration was performed, where the left inguinal canal revealed a peritoneal sac and sliding of the dilated left ureter behind the sac, with a significant change in diameter, corresponding to the paraperitoneal variant of ureteroinguinal herniation. Ligation of the sac and replacement of the ureter into the retroperitoneum were performed, with improvement in the hydronephrosis observed on the ultrasound 1 month after the intervention. However, 6 months later, hydronephrosis worsening as well as the obstructive pattern observed in the diuretic renogram required removal of the stenotic ureteral segment and reimplantation of the healthy proximal segment in the bladder by open approach (Cohen's reimplantation). Follow-up ultrasound of the renal tract showed no dilatation of the upper renal tract and the renal function tests were normal. Currently, the patient is 2 years old and he remains asymptomatic. In conclusion, s igns of ureteral obstruction such as hydronephrosis in patients with inguinal herniation may suggest the possibility of an ureteroinguinal hernia. Preoperative diagnostic suspicion is essential.

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一名 2 个月大婴儿的输尿管腹股沟疝气伴连续性输尿管狭窄:病例报告。
输尿管腹股沟疝在儿童中并不常见,迄今为止文献报道的病例很少,有可能导致梗阻性尿病。我们报告了一例在腹股沟疝修补术中发现的输尿管腹股沟疝,患者在出生前超声检查发现肾积水。一名 2 个月大的婴儿在产前患有左肾积水,并伴有左腹股沟肿块。术前超声检查显示左侧睾丸有一个产生肿块效应的回声管状图像,怀疑膀胱疝和/或输尿管向腹股沟管扩张。对患者进行了腹股沟开放手术探查,发现左侧腹股沟管内有腹膜囊,扩张的左侧输尿管在腹膜囊后滑动,直径有明显变化,这与输尿管腹股沟疝的腹膜旁变异型相符。患者接受了结扎输尿管囊并将输尿管置入腹膜后的手术,术后 1 个月,超声波检查发现肾积水有所改善。然而,6 个月后,肾积水恶化,利尿剂肾图上也观察到梗阻模式,因此需要切除狭窄的输尿管段,并通过开放式方法(科恩再植术)将健康的近端输尿管段重新植入膀胱。后续的肾道超声波检查显示上肾道没有扩张,肾功能检查也正常。目前,患者已经 2 岁,仍无任何症状。总之,腹股沟疝患者的输尿管梗阻症状(如肾积水)可能提示输尿管腹股沟疝的可能性。术前诊断怀疑至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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