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Journal articles on the topic 'Ectopic ureter'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Sardar, Mini, Gabriella Littler, Aakash Pai, and Amit Shetty. "Inverted Y Ureteral Duplication with Distal Obstructing Calculi in the Ectopic Ureter in the Prostatic Urethra." Journal of Endoluminal Endourology 6, no. 1 (2023): e10-e14. http://dx.doi.org/10.22374/jeleu.v6i1.154.

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Duplication of the ureter and renal pelvis is a relatively common congenital anomaly with an incidence of approximately 1 in 150 births. Different anatomical variations of ureteric duplication exist. Ectopic ureters are usually associated with ureteral duplication and a duplex collecting system. Duplication of the ureter ismore common unilaterally, has a female preponderance, and occurs more commonly on the left side.We present the case of a 58-year-old male with inverted Y ureteral duplication who had distal obstructing ureteric calculi in the ectopic distal ureteral opening in the prostatic

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Chama, Othman, Khalid Ouatar, Mustapha Ahsaini, et al. "Ureteral duplication with ectopic implantation of the ureter into the prostatic urethra." International Journal of Case Reports and Images 15, no. 1 (2024): 40–43. http://dx.doi.org/10.5348/101442z01oc2024cr.

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An ectopic ureter is a ureter that terminates in or below the bladder neck. The incidence of ectopic ureter remains unclear because this malformation is often asymptomatic. Eighty percent of ectopic ureters are associated with a duplicate ureter. In our case, it was a 29 years old man, who consulted for intermittent pelvic pain. The patient underwent a prostatic magnetic resonance imaging (MRI), which showed an ectopic ureteral abruption at the level of the prostate. The uroscanner showed a ureteral duplicity with a silent superior kidney.

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Paul, Sabyasachi, Ananya Mandal, Prithwis Mandal, and Pankaj K. Halder. "Surgical Challenges of Bilateral Duplex Kidney with Ectopic Ureters." D Y Patil Journal of Health Sciences 12, no. 1 (2024): 32–34. http://dx.doi.org/10.4103/dypj.dypj_69_23.

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Abstract The bilateral duplex system is extremely uncommon, and only a few cases have been documented in the literature. It may manifest as a bifid renal pelvis and partial or complete ureteric duplication, with or without ectopic insertion of the ureter. An ectopic ureter is more problematic when there is significant vesicoureteral reflux, incontinence, and/or blockage. The optimal course of treatment is considered to be ureteral reimplantation rather than heminephrectomy. We describe the management strategy for a case of bilateral duplex kidneys with bilateral ectopic ureters in a growing fe

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4

DE GROOTE, B., P. VAN LAER, K. MAURUS, J. P. VAN BIERVLIET, and L. MEEUS. "Embolization of Ectopic Kidney to Control Incontinence." Pediatrics 85, no. 2 (1990): 217–19. http://dx.doi.org/10.1542/peds.85.2.217.

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Ureteral ectopy in girls can cause dribbling incontinence if the ectopic ureter ends below the continence mechanism of bladder neck and external sphincter. Approximately 25% of ectopic ureters drain into the vagina. The corresponding renal tissue is often hypoplastic or dysplastic. Surgery used to be the treatment of choice. Depending on the quality of the corresponding renal tissue, one had the choice between ureter reimplantation or partial or total nephrectomy. We succeeded in treating a girl with a hypoplastic kidney and an ectopic ureter nonsurgically by embolizing the corresponding renal

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5

Mazhar Ali, Kumail Sajjad, and Qazi Naeem. "Laparoscopic reimplantation of ectopic ureter in adult girl, first case report in Pakistan." Professional Medical Journal 30, no. 01 (2023): 142–45. http://dx.doi.org/10.29309/tpmj/2023.30.01.7328.

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Duplex collecting system is commonly associated with ectopic ureter in females. A 17 years old girl presented with continuous urinary dribbling since birth in our OPD and she also had urge to void. This is a rare case with double ureteral ectopia and this case report enlightens the suffering of rare diseased in terms of diagnosis and treatment. She had been frequently treated for urinary tract infections. The surgical treatment is the main stay which comprises the en bloc reimplantation of ectopic ureter via open surgical or laparoscopic approach. To our knowledge yet, laparoscopic reimplantat

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6

Tang, Min, Quanrongzi Wang, Bianjiang Liu, et al. "Single ectopic ureteral orifice with bilateral duplicated renal collecting systems in an adult girl: Diagnosis by magnetic resonance urography." Canadian Urological Association Journal 9, no. 7-8 (2015): 554. http://dx.doi.org/10.5489/cuaj.2886.

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Renal duplication accompanied by ureteral ectopia is an uncommon urinary congenital abnormality. We report the case of a 21-year-old girl who suffered from lifelong continuous urinary leakage. She was finally diagnosed with bilateral duplicated collecting systems complicated with right ectopic ureteral orifice – an extremely rare case. The patient underwent ureteric re-implantation for the ectopic side, and her urinary incontinence ceased soon thereafter. In this case, traditional imaging failed to show the exact insertion of an ectopic ureter. However, magnetic resonance urography combined wi

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Grbic, Dragan, Dimitrije Jeremic, Sasa Vojinov, Milan Popov, and Goran Marusic. "Renal dysplasia with the ipsilateral ectopic ureter mimicking abscess of the prostate." Vojnosanitetski pregled 71, no. 2 (2014): 211–13. http://dx.doi.org/10.2298/vsp1402211g.

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Introduction. In males the ectopic ureter usualy drains into the prostate (50%). During ureteric developement a thin membrane (Chawalla?s membrane) separates the lumen of the ureter and the urogenital sinus at the point where the ureter joins the urogenital sinus. This membrane ruptures allowing urin to drain from the ureter to the urogenital sinus. The authors reported a case of renal dysplasia associated with ipsilateral uretral ectopia mimicking prostatic abscess. Case report. A subfebrile (37.3?C), 23-year-old patient, otherwise healthy, presented with persistent ascending perineal pain no

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8

Mishra, Kirtishri, and Christopher S. Elliott. "A violation of the Weigert-Meyer law – an ectopic ureter arising from the lower renal pole." Journal of Clinical Urology 10, no. 3 (2015): 202–4. http://dx.doi.org/10.1177/2051415815570651.

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Ectopic ureters are a found in one of every 2000–4000 people. This abnormality can present with urinary tract infections, haematuria, and occasionally incontinence. Ectopic ureters traditionally follow the Weigert-Meyer Law, which describes the relationship of the lower and upper renal moieties. It states that the lower renal pole drains into a laterocranial ureteral orifice (and may reflux), while the upper renal pole drains into a mediocaudal ureteral orifice (and may be obstructed). If a duplicated ureter does not insert into the bladder, it by rule, originates from the upper pole. We prese

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Sneha, P. John, Ghorpade Mayuri, Borkar Meenakshi, Verma Shobha, Bhoir Mehera, and Nakhate Manisha. "Bifid Ureter: A Cadaveric Study." International Journal of Pharmaceutical and Clinical Research 16, no. 1 (2024): 188–97. https://doi.org/10.5281/zenodo.11094008.

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Bifid Ureter is a condition where upper end of the ureter is bifid. In the lower part of the course two ureters join together to open by a common orifice into the urinary bladder. It occurs due to premature division of ureteric bud. <strong>Aim: </strong>To study any anomalies of ureter in routine anatomical dissection. <strong>Methods:</strong> 50 cadavers of both sexes that had been fixed in formalin were used in the current study. During the dissection, the ureter’s anatomy was the main point of attention. From the renal pelvis to the uretrovesical junction, which

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Grover, Jitendra Kumar, Deepak Kumar Soni, and Shehtaj Khan. "Successful management of single system ectopic ureter with preserved renal function in a female child: a case report." International Surgery Journal 8, no. 3 (2021): 1033. http://dx.doi.org/10.18203/2349-2902.isj20210944.

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Ectopic ureter is a rare congenital anomaly of the genitourinary system, in which ureter does not insert into its normal anatomical position in bladder. Incidence is 1 in 4000 and has female predominance. Ectopic ureter is generally (80-85%) associated with a duplication of renal system, while in single system is found in 15-20%. If ectopic ureter drains a single kidney it is known as single system ectopic ureter (SSEU) in a female is extremely rarely found. Here, we report a case of single system ectopic ureter without renal dysplasia and other congenital abnormalities, which was diagnosed an

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Oliveira, Ana Caroline Costa de, Angélica Andrade Guimarães, Thais Lisboa Machado Romano, Daniel Herreira Jarrouge, and Daniel de Souza Ramos Angrimani. "Surgical correction of bilateral ectopic ureter using the neoureterocystostomy technique." Brazilian Journal of Veterinary Research and Animal Science 58 (July 13, 2021): e182499. http://dx.doi.org/10.11606/issn.1678-4456.bjvras.2021.182499.

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Ureteral ectopy is a rare disorder in the small animals’ clinic. It is characterized as a congenital anomaly, resulting from the ducts differentiation failure during embryogenesis. In this scenario, the ureters present themselves outside the anatomical site, being inserted into the uterus, urethra, urinary vesicle neck, or vagina. The clinical signs are urinary incontinence and perivulvar dermatitis. Surgery is the accepted treatment to correct the anomaly. The surgical procedure is based on relocating the ectopic ureter and treating associated modifications. This report describes a case of in

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Benabdallah, Y. Staouni. "Renal Ectopia in the Pelvic Area: A Rare Case." Scholars Journal of Medical Case Reports 12, no. 01 (2024): 15–17. http://dx.doi.org/10.36347/sjmcr.2024.v12i01.005.

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Renal ectopia is a positional defect during development, consistently accompanied by malrotation, always involving abnormal vascularization with one or more ectopic arteries and a ureter of appropriate length for the location of the kidney. It is distinct from renal ptosis. Several types of ectopias are distinguished: on one hand, simple ectopias occurring in the vertical direction (intrathoracic kidney, low-lying kidney) or in the transverse direction (crossed ectopia), and on the other hand, ectopias with symphyses. Pathological pelvic ectopic kidney is rare. It is often revealed by pain, in

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13

Prządka, Przemysław, Bartłomiej Liszka, Ludwika Gąsior, et al. "Laparoscopic ureteroneocystostomy in the treatment of urinary incontinence due to ectopy of the ureters in female dogs: A pilot study." PLOS ONE 18, no. 10 (2023): e0292485. http://dx.doi.org/10.1371/journal.pone.0292485.

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Ureteral ectopia is rare and requires surgical treatment after a thorough diagnostic workup. Open surgical techniques for repositioning ectopic ureters have been known for many years and are well described in the literature. However, to the best of our knowledge, no laparoscopic method of correcting this pathology has been described, which, in our opinion, would benefit the animal in terms of the healing process and overall clinical outcomes. This study aimed to evaluate the possibility of laparoscopic treatment of ureteral ectopia, which causes urinary incontinence in dogs. All of the operate

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14

Atanasov, Emil, Ivan Aleksandar Georgiev, Simeon Andreev, and Martin Tsanev. "Laparoscopic terminolateral ipsilateral uretero-uretero anastomosis in a child with ureteral ectopy of duplex kidney and upper pole hydronephrosis." Journal of Endourology and Minimally Invasive Surgery 13, no. 1 (2025): 14–15. https://doi.org/10.57045/jemis/1310425.pp14-15.

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Introduction: An ectopic ureter is an anomaly in which the ureter has a non-orthotopic distal insertion (not in the bladder trigonum). It has incidence of 1:4000, and it is two to three times more frequent in women. 80% of women with an ectopic ureter have a duplex kidney, and in 80% of the cases the ectopic ureter originates form the upper pole. In 69% of the cases the ectopic ureter has an insertion in the bladder neck or in the urethra, in 31% in the vagina. In men – the insertion is in the posterior urethra - 57%, seminal vesicles - 33%, vas deferens - 10%. The ectopic ureter can be obstru

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15

Yoon, Hun-Young, F. A. Mann, John P. Punke, and Soon-wuk Jeong. "Bilateral Ureteral Ectopia With Renal Dysplasia and Urolithiasis in a Dog." Journal of the American Animal Hospital Association 46, no. 3 (2010): 209–14. http://dx.doi.org/10.5326/0460209.

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A 7-month-old, 4.3-kg, spayed female bichon frise was referred for evaluation of chronic urinary incontinence. Abdominal radiographs revealed calculi within the right kidney and ureter. An ultrasound revealed a small right kidney. An abdominal computed tomography scan with contrast revealed that the left ureter was extramurally ectopic, inserting into the proximal urethra. A right intramural ectopic ureter was identified during cystotomy. Ureteronephrectomy was performed on the right, and ureteroneocystostomy was performed on the left. A telephone conversation with the owner 4 months after sur

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Agarwal, Varun, and Ojas Vijayanand Potdar. "A Documented Rare Case of a Duplicated Renal Collecting System with Ectopic Opening into the Vagina Managed with Robotic Assisted Heminephrectomy of the Non- Functioning Upper Moiety." NATIONAL BOARD OF EXAMINATIONS JOURNAL OF MEDICAL SCIENCES 2, no. 6 (2024): 634–44. http://dx.doi.org/10.61770/nbejms.2024.v02.i06.014.

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Background: The definition of ectopic ureter is an abnormal opening of the ureter (single or duplex) that does not open in the trigonal region of the bladder. In 80% of these cases, ectopic ureter is associated with complete duplication. The upper moiety of a duplex kidney is usually the origin of a ectopic ureter in most of the cases. The opening of the ectopic ureteric in females can be anywhere from bladder neck to perineum with urethra, vagina, and vestibule. Duplex kidney, also known as duplex collecting system, is a common congenital urinary system anomaly with a morbidity of about 0.8–1

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17

International, Journal of Medical Science and Innovative Research (IJMSIR). "Congenital Uretero-Vaginal Fistula - A Rare Case of Single System Ectopic Ureter Associated with Renal Dysplasia." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 5 (2024): 143–47. https://doi.org/10.5281/zenodo.15437480.

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<strong>Abstract</strong> Urinary incontinence resulting from functional disturbances is common in childhood, however diagnosis of urinary incontinence due to organic causes such as ectopic ureter and genital fistulas is important because urinary continence in females has a negative impact on the quality of life and correct diagnosis carries a potential of absolute treatment by surgical corrections. We present a case of a 9-year-old female with complaints of involuntary leakage of urine from the vagina despite normal bladder filling and emptying. A diagnosis of ectopic ureter with uretero-vagi

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Duffy, Maura, and Alex Gallagher. "Encrusted Cystitis with Suspected Ureteral Obstruction Following Cystoscopic-Guided Laser Ablation of Ectopic Ureters in a Dog." Journal of the American Animal Hospital Association 54, no. 2 (2018): 117–23. http://dx.doi.org/10.5326/jaaha-ms-6392.

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ABSTRACT A 1 yr old 30 kg spayed female Labrador retriever presented for stranguria and hematuria 3 wk after cystoscopic laser ablation for ectopic ureters. Encrusted cystitis was diagnosed based on ultrasonography, cystoscopy, urinalysis, and culture of Corynebacterium urealyticum from the urine. Unilateral hydronephrosis and hydroureter were suspected to be secondary to obstruction at the trigone. The dog was treated with focal debridement of plaques at the left ureter, urinary acidification, and long-term antibiotic therapy with complete recovery. This is the first report of encrusted cysti

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Chida, Naoki, Seiichi Orikasa, Ryuichiro Konda, Masaru Takahashi, Shigeto Ishidoya, and Yukihiko Ogata. "Crossed Ureteral Ectopia with an Ectopic Blind-Ending Ureter." Urologia Internationalis 55, no. 3 (1995): 169–72. http://dx.doi.org/10.1159/000282779.

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Heijkoop, Bridget, John Lahoud, and Eddy Lee Hao Wong. "Endoscopic stone management in an ectopic ureter inserting into the prostatic urethra." BMJ Case Reports 16, no. 9 (2023): e254927. http://dx.doi.org/10.1136/bcr-2023-254927.

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We report a case of successful endoscopic stone management in a patient with ectopic ureteric insertion. The patient had a complete duplex collecting system, with the upper moiety ureter inserting ectopically into his prostatic urethra, and an obstructing ureteric stone in the distal portion of the ectopic ureter. This made both characterisation of the patient’s anatomy and initial emergency stone management challenging.The case offers several learning points for clinicians who may encounter similar situations. By describing the challenges of managing this patient’s presentation, we highlight

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Goidescu, Iulian Gabriel, Georgiana Nemeti, Adelina Staicu, et al. "Prenatal Diagnosis of Vaginal Ectopic Ureter Insertion—Case Outcome and Literature Overview." Diagnostics 15, no. 14 (2025): 1788. https://doi.org/10.3390/diagnostics15141788.

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Background and clinical significance: Ectopic ureters are a rare urinary tract malformation, typically diagnosed in childhood and infrequently in adulthood. The prenatal detection by ultrasound and magnetic resonance imaging (MRI) of this clinical entity has scarcely been reported. Careful foetal scanning during the late second and third trimester might provide clues and lead to prenatal detection. However, even the postnatal diagnosis is challenging, and often delayed towards adulthood, since the condition may present with nonspecific symptoms, leading to underdiagnosis or misdiagnosis. In fe

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Prameswari, Larasita, and Suharjendro. "LITERATURE REVIEW: ECTOPIC URETER IN CHILDHOOD." Lombok Health And Science Journal 2, no. 1 (2023): 18–31. http://dx.doi.org/10.29303/lhsj.v2i1.2504.

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Ectopic ureter is a rare and often overlooked disorder of the urinary tract that can cause urinary incontinence. Ectopic ureter is thought to be caused by the ureteral bud failing to separate from the mesonephric duct, resulting in more caudal insertion. This anomaly is related to genitourinary tract embryogenesis, which results in differences in anatomical and clinical manifestations between male and female. Delayed diagnosis and treatment resulted in years of suffering and disruption to social development and school years. The urinary incontinence due to this anomaly can also cause stress ur

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Heywood, Shirley, and Shuvechchha Dewa Shrestha. "Diagnosis and management of ectopic ureter in a low resource setting – A case series." Nepal Journal of Obstetrics and Gynaecology 16, no. 2 (2022): 105–12. http://dx.doi.org/10.3126/njog.v16i2.42111.

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Aims: To review the experience of women and girls treated for ectopic ureter in Surkhet through the fistula camps and Fistula Treatment Centre and analyse the diagnostic method, management and outcome. Methods: This was a retrospective study of the patients with ectopic ureter who received treatment in Surkhet since 2009. Data were analysed from patient records and interviews. Results: Seven patients were diagnosed with ectopic ureter over a period of 12 years. Five patients were prepubertal with age range of 7 - 15 years. History of continuous incontinence with normal voiding was

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Kuzovleva, G. I., V. V. Rostovskaya, O. V. Staroverov, E. K. Ayryan, N. A. Khvatynets, and G. A. Korolev. "Ectopic ureter in a patient with a non-duplex hypoplastic kidney." Voprosy praktičeskoj pediatrii 17, no. 4 (2022): 151–54. http://dx.doi.org/10.20953/1817-7646-2022-4-151-154.

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Ectopic ureter (EU) is a rare urinary tract malformation often found in patients with a duplex kidney. Abnormal location of the ureteral orifice in a non-duplex kidney is observed in 20–25% cases of all ectopias. The paraurethral EU is described in very few publications. An 8-year-old female patient complained of periodic abdominal pain, inflammatory changes in the urinary sediment, and periodic urinary incontinence. The child had not been examined earlier. Ultrasonography findings: left kidney size 41 × 20mm; the ureter was dilated along its entire length and has bends; the diameters of its u

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Kanali, O., H. Chenter, K. Outaghyame, et al. "A Case of Chronic Back Pain: Revealing Complete Ureteral Duplicity in an Adult Woman." SAS Journal of Medicine 10, no. 10 (2024): 1056–58. http://dx.doi.org/10.36347/sasjm.2024.v10i10.012.

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Ureteral duplication is a rare congenital anomaly, often diagnosed incidentally, characterized by the presence of two distinct ureters draining a single kidney. This condition can lead to complications such as vesicoureteral reflux or upper pole obstruction, often due to ectopic ureteral insertion or ureterocele. We report the case of a 40-year-old woman presenting with left-sided chronic low-back pain. Imaging studies, including ultrasound and CT urography, revealed bilateral ureteral duplication with significant left ureterohydronephrosis due to dysplasia and ectopic insertion of the upper u

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Vryblevskiy, S. G., I. V. Poddubniy, O. S. Shmyrov, et al. "LAPAROSCOPIC REIMPLANTATION FOR THE MANAGEMENT OF URETERAL DUPLICATIONS WITH PRIMARY MEGAURETERS IN CHILDREN." Russian Journal of Pediatric Surgery 22, no. 6 (2018): 306–8. http://dx.doi.org/10.18821/1560-9510-2018-22-6-306-308.

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Ureteral duplication is an abnormality of the urogenital tract, which may be presented in about 0,8% of the population. However, in some cases, a complete doubling of the collective system is combined with such defects as megaureter, ureterocele, vesicoureteral reflux, urinary incontinence, and others. Currently, there are several treatment options for children with urological pathology in the doubling of the kidneys. Depending on the type of pathology and the functional state of the affected segment, this can be both organ-bearing operations (heminephrouretherectomy), and reconstructive plast

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MA, Rui, Rong-de WU, Wei LIU, et al. "A new classification of duplex kidney based on kidney morphology and management." Chinese Medical Journal 126, no. 4 (2013): 615–19. http://dx.doi.org/10.3760/cma.j.issn.0366-6999.20121259.

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Background The initial classic classification of duplex kidney into complete (two ureters) and incomplete (“Y” shaped ureter) types are based on the ureter status. At the meantime, the features of the upper and lower moieties of duplex kidney were very crucial for appropriate procedure of hemi-nephrectomy, which was most commonly used for addressing the issues caused by a duplex kidney; and recently more applications of laparoscopy were used. In this study, we aimed prudently to propose a new classification based on the features of the upper and lower moieties of duplex kidney. Methods Sixty-f

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Rauf, Rafikah, Bambang Soeprijanto, Indrastuti Normahayu, and Lenny Violetta. "URETEROCELE DENGAN DUPLIKASI URETER KOMPLIT." Jurnal Radiologi Indonesia 4, no. 1 (2020): 1–7. http://dx.doi.org/10.33748/jradidn.v4i1.82.

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Ureterocele is a congenital distal ureter dilatation abnormality that formed like sac located intravesical or ectopic outside the normal anatomy location. The exact etiology of ureterocele is not yet known certainty, presumably due to the obstruction of the ureteral orificium during embryogenesis. There are 80% ureterocele associated with urinarius duplicating system. Radiological examination has an important role in the evaluation and diagnosis of ureterocele. We reported a case of 2 year 7 monthold girl admitted to the hospital with complaints of pain during urination experienced since 2 mon

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Straub, Péter, Gyula Horváth, Sándor Dávidovics, and András Pintér. "Magnetic resonance urography in the diagnosis of the ectopic ureters." Orvosi Hetilap 148, no. 3 (2007): 105–9. http://dx.doi.org/10.1556/oh.2007.27887.

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Bevezetés: Ectopiás ureterek kórismézése gyermekkorban hagyományos diagnosztikai eljárásokkal (fizikális, ultrahangvizsgálat, intravénás urográfia, mictiós cisztouretrográfia, uretrocisztoszkópia, izotópvizsgálatok) számos esetben nem lehetséges. Célkitűzés: A szerzők célja egy viszonylag új vizsgálómódszer, a mágneses rezonancia urográfia (MRU) ismertetése a más módszerekkel csak nehezen, vagy nem diagnosztizálható ectopiás ureterek kimutatására gyermekkorban. Módszer: A tanulmányban részt vevő osztályok beteganyagában az elmúlt 3 évben 7 leányban alkalmazták az MRU-t ectopiás ureterek kimuta

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Manley, Jonathan, Ferekh Salim, and Jake Patterson. "Antegrade Ureteroscopy for an Obstructing Distal Ureteric Stone in a Partial Duplex System with Ectopic Distal Insertion." Journal of Endoluminal Endourology 2, no. 4 (2019): e20-e22. http://dx.doi.org/10.22374/jeleu.v2i4.68.

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Urinary tract abnormalities such as ureteric duplication and ectopic insertion may result in difficulty accessing the distal ureter to treat obstructing stones. This case illustrates the feasibility of treating distal ureteric stones with antegrade flexible ureteroscopy.

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Buli, P., G. D'Amato, A. Bertaccini, et al. "Ectopic ureter: Case report." Urologia Journal 59, no. 1_suppl (1992): 226–29. http://dx.doi.org/10.1177/039156039205901s74.

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An ectopic ureter is one which opens anywhere other than on the posterolateral extremity of the trigone and is an uncommon urological anomaly with a female predominance. The aim of this study is to consider an unusual case of ectopic ureter with a large distal diverticula simulating a bladder duplicity.

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Wewoli, Bentil A., and Akisibadek A. Afoko. "Vesicovaginal Fistula Secondary to Left Ectopic Ureter in a 3-Year-Old Female with Left Ureter-Duplication in Tamale Teaching Hospital, Ghana: A Case Report." International Journal of Health, Medicine and Nursing Practice 6, no. 5 (2024): 47–53. http://dx.doi.org/10.47941/ijhmnp.2007.

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Purpose: Vesicovaginal fistula (VVF) is a pathological connection between the bladder and vagina, primarily caused by gynaecological surgery, obstructed labour, and cesarean section. VVF significantly impairs quality of life and is prevalent in developing countries, with Africa seeing up to 130,000 new cases annually. Surgical repair, especially transvaginal approaches, remains the primary treatment. Paediatric cases of VVF, often linked to congenital anomalies like ectopic ureter, are rare and complex to manage. Methodology: We report a case of a 3-year-old female with continuous urinary leak

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Saputro, Johan Eko, and Sofyan Rais Addin. "095. A Rare Case Report: A 10-Years-Old Girl with Ectopic Ureter and Ectopic Hypoplasia Kidney." JBN (Jurnal Bedah Nasional) 8, no. 2 (2024): 95. http://dx.doi.org/10.24843/jbn.2024.v08.is02.p095.

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Background: The urinary tract system develops from an embryological structure in the dorsal part of the embryo, the intermediate mesoderm, which develops between the 4th and 10th week of gestation. During the embryogenesis process, disturbed metanephric mesenchyme can cause congenital abnormalities of the kidneys and urinary tract (CAKUT), one of which is ectopic abnormalities. Ectopic ureter and ectopic kidney had an incidence of 1:2000 and 1:3000 worldwide, respectively. Additionally, this rare case will be even more uncommon with the presence of a hypoplasia kidney. These anomalies contribu

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Passerini Glazel, G., C. Milani, P. Bassi, L. Chiozza, G. Rizzoni, and F. Pagano. "Bilateral Single Ectopic Ureter." European Urology 14, no. 6 (1988): 454–57. http://dx.doi.org/10.1159/000473008.

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Wakhlu, Dalela, Tandon, Chandra, and Wakhlu. "The single ectopic ureter." BJU International 82, no. 2 (1998): 246–51. http://dx.doi.org/10.1046/j.1464-410x.1998.00719.x.

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de la Hunt, M. N. "The single ectopic ureter." Journal of Pediatric Surgery 34, no. 6 (1999): 1049. http://dx.doi.org/10.1016/s0022-3468(99)90816-3.

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Esteban, Jacinto, and Adrian Gutierrez. "Bilateral single ectopic ureter." Urology 31, no. 2 (1988): 138–39. http://dx.doi.org/10.1016/0090-4295(88)90039-8.

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Onwuasoanya, U. E., R. K. Agrawal, H. O. Ekwuazi, et al. "Ectopic pelvic kidney associated with uretero-pelvic junction obstruction: a case report." KIDNEYS 13, no. 3 (2024): 233–35. http://dx.doi.org/10.22141/2307-1257.13.3.2024.469.

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Ectopic kidneys though uncommon can be associated with other anomalies of the genitourinary system such as uretero-pelvic junction obstruction, vesicoureteral reflux and upper urinary tract abnormalities. These associations present surgical challenges in an ectopic kidney. We report the surgical management of a right ectopic kidney associated with uretero-pelvic junction obstruction and severe hydronephrosis. A 27-year-old male presented to Zenith Medical and Kidney Center in Abuja with complaints of recurrent, dull right flank pain of 1 year duration. Physical examination revealed a non-tende

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Aditi, Vohra, ,Ranjan Kumar, and ,Narula Harneet. "URETERAL TRIPLICATION WITH STRICTURE OF MIDDLE URETER AND ECTOPIC INSERTION OF URETER." International Journal of Advanced Research 4, no. 5 (2016): 1498–502. http://dx.doi.org/10.21474/ijar01/482.

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Engelstein, Dov, Pinhas M. Livne, Maya Cohen, and Ciro Servadio. "Type ii ureteral triplication associated with ectopic ureter." Urology 48, no. 5 (1996): 786–88. http://dx.doi.org/10.1016/s0090-4295(96)00323-8.

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Chatterjee, Sunayana, Hrishikesh Deshmukh, and Vaibhav Thorat. "Rare presentation of ureteral duplication: stone localization in the upper moiety." International Journal of Research in Medical Sciences 11, no. 10 (2023): 3866–68. http://dx.doi.org/10.18203/2320-6012.ijrms20233048.

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This case report describes a rare exception to the typical presentation of complete ureteral duplication, a relatively uncommon condition in comparison to single ureter or partial duplication. The patient presented with right flank pain and imaging revealed a duplex collecting system with a stone located in the upper moiety. Upper moiety complications, such as ectopic ureteric insertion and multicystic dysplastic moiety, are usually observed in duplex kidneys. Contrast-enhanced imaging and endoscopic treatment were utilized for accurate diagnosis and management. The case deviates from the expe

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Eisele, Jason G., Joshua Jackson, and Dave Hager. "Ectopic Ureterocele in a Cat." Journal of the American Animal Hospital Association 41, no. 5 (2005): 332–35. http://dx.doi.org/10.5326/0410332.

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A 9-month-old, castrated male domestic shorthair cat with urinary incontinence was referred for surgical correction of an ectopic ureter. Excretory urography revealed hydronephrosis of the right kidney, right hydroureter, and ureterocele. A partial ureterocelectomy and neoureterocystostomy were performed. This report describes the surgical modification of the ureterocele and ectopic ureter to correct ipsilateral hydronephrosis, hydroureter, and urinary incontinence.

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Wang, Qijing, Zaigui Wu, Fengbin Zhang, et al. "Gynecological Diagnosis and Treatment of Ectopic Ureter Insertion into Vagina: Analysis of Five Cases and a Literature Review." Journal of Clinical Medicine 11, no. 21 (2022): 6267. http://dx.doi.org/10.3390/jcm11216267.

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An ectopic ureter is a ureter that does not correctly connect to the trigone of the bladder and drains outside of the bladder. Here, we presented five cases of ectopic ureter opening into the vagina, whose clinical symptoms and malformations were rarely described in previous case reports. All five patients were hospitalized with complaints of gynecologic disease. Three of the five cases did not present the typical symptoms of urinary incontinence. Three of these cases showed congenital malformations of the female genital tract. Four cases were diagnosed in adulthood. All patients were analyzed

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Narcı, Adnan, Mevlit Korkmaz, Muhittin Karakus, Tolga Altug Sen, Îlhamı Surer, and Salih Cetinkursun. "Cross ectopic multicystic dysplastic kidney with ureterocele in nonectopic site." Canadian Urological Association Journal 4, no. 3 (2013): 61. http://dx.doi.org/10.5489/cuaj.858.

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Crossed renal ectopy (CRE) is the second most common fusionanomaly of the kidney, with an incidence of 1 in 7000 autopsies;it comes in second after horseshoe kidney. Crossed renal ectopy isassociated with an ectopic ureter and generally an ectopic kidneyfused with a normal kidney. A 7-month-old boy who had left-torightcrossed non-fused renal ectopy and multicystic renal dysplasiawith ureterocele in nonectopic kidney was reported in Englishlanguage literature. In this article, we present the first case of CREwhere surgical intervention has been performed.

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Chandna, Abhishek, Pawan Kaundal, Kalpesh Mahesh Parmar, and Shrawan Kumar Singh. "Dismembered extravesical reimplantation of ectopic ureter in duplex kidney with incontinence." BMJ Case Reports 13, no. 8 (2020): e234915. http://dx.doi.org/10.1136/bcr-2020-234915.

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Ectopic ureter is a rare but pertinent cause of incontinence in young women. We report a 12-year-old girl who presented with reports of incontinence since birth. She was evaluated and found to have complete duplication of the left ureter, with the upper moiety ureter opening into the vestibule of the vagina just below the external urethra meatus. She was managed surgically by dismembered extravesical reimplantation of the upper moiety ureter instead of the conventional method of common sheath reimplantation, sparing the patient a wide cystostomy and intravesical dissection. One year postsurger

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Heier, Evelyn, Christine Urban, Ahmed Abdellatif, Cetina Thiel, and Reto Neiger. "Assessment of individual kidney function in a dog with congenital anomalies of the urinary tract." Veterinary Record Case Reports 7, no. 2 (2019): e000753. http://dx.doi.org/10.1136/vetreccr-2018-000753.

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A 21-month-old entire female labrador retriever was presented for polyuria, pollakiuria, haematuria and intermittent urinary incontinence. Clinical signs were absent during antibiotic treatment but reoccurred shortly after completion of a treatment course. Investigations detected bilaterally dilated ureters, right renal hypoplasia, left extramural ectopic ureter and right intramural ectopic ureter forming an ureterocoele. Blood tests revealed moderate renal azotaemia. 99mTc-DMSA (technetium-99m-dimercaptosuccinic acid) scintigraphy was used to quantify individual kidney function to carefully c

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Tuncer, Korhan, Gizem Kilinc, Ismail Sert, Goksever Akpinar, and Cem Tugmen. "Ectopic ureter associated with Zinner’s syndrome in a kidney recipient: case report and literature review." Revista da Associação Médica Brasileira 66, no. 5 (2020): 692–95. http://dx.doi.org/10.1590/1806-9282.66.5.692.

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SUMMARY INTRODUCTION Zinner’s Syndrome is a triad of mesonephric duct anomalies comprising unilateral renal agenesis, seminal vesicle cyst, and ejaculatory duct obstruction. In this study, we present a kidney recipient with ectopic ureter associated with Zinner’s syndrome and a literature review. CASE PRESENTATION A 59-year-old male with a history of chronic kidney disease and left renal agenesis underwent deceased donor kidney transplantation. After securing optimal renal functions, the patient underwent abdominal computed tomography (CT) scan for the seroma that occurred under the incision.

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Mori, Yoshinori, Hidekazu Takiuchi, Michio Nojima, et al. "ECTOPIC URETER IN 54 CHILDREN." Japanese Journal of Urology 92, no. 3 (2001): 470–73. http://dx.doi.org/10.5980/jpnjurol1989.92.470.

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KEANE, T., A. OWENS, and D. KELLY. "Bilateral Obstructed Ectopic Duplex Ureter." British Journal of Urology 60, no. 1 (1987): 82–83. http://dx.doi.org/10.1111/j.1464-410x.1987.tb09145.x.

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MacDonald, Gordon R. "The Ectopic Ureter in Men." Journal of Urology 135, no. 6 (1986): 1269–71. http://dx.doi.org/10.1016/s0022-5347(17)46068-x.

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