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A Case of Left Duplex Kidney with Hydronephrosis Mimicking a Left Renal Cyst in a 29-Year-Old Woman

机译:左双相肾脏伴有肾内肾脏,在一名29岁的女性中模仿左肾囊肿

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Patient: Female, 29-year-old Final Diagnosis: Left duplicated kidney with upper moiety severe hydronephrosis Symptoms: Left side abdominal pain Medication: — Clinical Procedure: Robot-assisted left heminephrectom Specialty: Surgery ? Urology Objective: Congenital defects/diseases Background: Duplex kidney, also known as duplex renal collecting system, consists of 2 ureters arising from a single kidney and is a common congenital anomaly. The condition is usually an asymptomatic normal variant. However, abnormal anatomic variants such as hydronephrosis, vesicoureteral reflux (VUR), and ureterocele are sometimes observed in a patient with a duplicated kidney. These abnormal variants usually lead to diagnostic challenges. Here, we report a case of congenital left duplex kidney with hydronephrosis that presented as an isolated left renal cyst in a 29-year-old woman. Case Report: We present the case of a 29-year-old woman who had left-side abdominal pain and fever for 1 day. Left-side flank throbbing pain was also noted. Laboratory investigations showed leukocytosis, pyuria and bacteriuria. Renal ultrasound revealed a huge hypoechoic mass around the left kidney, which was suspected to be a huge renal cyst or renal abscess. Under the impression of acute pyelonephritis with abscess formation, the patient was admitted for antibiotic treatment. The following abdominal computed tomography (CT) revealed a left duplex kidney with severe hydronephrosis and hydroureter. A percutaneous nephrostomy was then performed. Next, following a discussion with the patient, she underwent a robot-assisted left heminephrectomy. Conclusions: A duplex kidney and collecting system should be considered when chronic urologic problems occur. This report shows that because duplex kidney is a relatively common congenital abnormality, it should be considered in the differential diagnosis in young patients who present with renal cyst. This case also shows that patients can be managed effectively using robot-assisted heminephrectomy.
机译:患者:女,29岁的最终诊断:左侧部分严重肾内症状左侧腹部疼痛药物: - 临床手术:机器人辅助左升肺胶凝特产:手术?泌尿外科目的:先天性缺陷/疾病背景:双链肾,也称为双链肾脏收集系统,由单个肾脏产生的2次输尿管组成,是一个常见的先天性异常。条件通常是无症状的正常变体。然而,有时在肾脏重复的患者中观察有时会观察到肾内肾小分,肾外衰分,血管内反流(VUR)等异常解剖学变体。这些异常变种通常导致诊断挑战。在这里,我们报告了一个先天性左双链肾的病例,其肾内肾病呈现为一名29岁女性的左肾囊肿。案例报告:我们提出了一个29岁女性的案件,左侧腹痛和发烧1天。还注意到左侧侧翼悸动疼痛。实验室调查显示白细胞增多症,脓尿和细菌。肾超声揭示了左肾周围的巨大的低压尸体,怀疑是一种巨大的肾囊肿或肾脏脓肿。在急性肾盂肾炎的印象下,患者被诱导抗生素治疗。以下腹部计算断层扫描(CT)揭示了左双链肾,具有严重的肾内肾小粒和循环。然后进行经皮肾病术。接下来,在与患者讨论之后,她经历了一种机器人辅助左血红蛋白。结论:在慢性泌尿科问题发生时,应考虑双链肾脏和收集系统。本报告显示,由于双相肾是一种相对常见的先天性异常,应该考虑患有肾囊肿的年轻患者的差异诊断。这种情况还表明,患者可以使用机器人辅助碘睫毛切除术治疗。

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