scholarly journals Crossed renal ectopia with fusion in a female feline: case report

2019 ◽  
Vol 71 (3) ◽  
pp. 833-836 ◽  
Author(s):  
J.Q. Fulgêncio ◽  
F.G. Miranda ◽  
C.J. Santos ◽  
G.D. Moreira ◽  
R.C.S. Tôrres ◽  
...  
Keyword(s):  
Renal Function ◽  
Case Report ◽  
Diagnostic Imaging ◽  
Final Diagnosis ◽  
Excretory Urography ◽  
Abdominal Ultrasonography ◽  
Renal Ectopia ◽  
Mixed Breed ◽  
Crossed Renal Ectopia ◽  
The Right

ABSTRACT A 3 year old female feline of mixed breed was sent to the diagnostic imaging sector under suspicion of bleeding due to ovariohysterectomy. An abdominal ultrasonography was performed to confirm the initial suspicion. However, no signs of bleeding were found, instead it was observed that the left renal silhouette had two pelvises and was elongated and larger than normal. The right kidney was not found. Excretory urography was requested to evaluate the condition of the ureters. The final diagnosis was crossed renal ectopia with fusion in an asymptomatic cat with no changes in renal function.

scholarly journals Crossed renal ectopia with an unusual form of fusion (inverted U shape) managed by novel approach - laparoscopic ureterocalicostomy. A case report

2021 ◽  
Vol 6 (1) ◽  
pp. 71-75
Author(s):  
Osama Bani Hani ◽  
Omar Halalsheh ◽  
Yazeed Mohammad ◽  
Anas Bani Yaseen ◽  
Ruba Khasawneh ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Presentation ◽  
The Body ◽  
Published Data ◽  
Renal Ectopia ◽  
Novel Approach ◽  
Crossed Renal Ectopia ◽  
The Right ◽  
Tract Infections ◽  
Unusual Type

Herein we present a case of crossed renal ectopia with an unusual type of fusion, discovered incidentally in a 11-year-old girl presented with recurrent urinary tract infections. Both kidneys were located on the right side of the body fused in their upper poles only, forming an inverted U shape. After reviewing the published data on this topic, we found that most of the described anomalies were within the six well-known types of fusion anomalies. This child had an unusual clinical presentation of severe hydronephrosis of the orthotopic kidney. A unique surgical technique to correct the pathology to be able to preserve the residual mass of that kidney was performed.

scholarly journals Supernumerary Nipples, Congenital Scoliosis, Spina Bifida, Diastematomyelia, and Crossed Renal Ectopia in a child

2016 ◽  
Vol 3 (2) ◽  
pp. 55
Author(s):  
Kiran Panthee ◽  
Kiran Sharma ◽  
Balkrishna Kalakheti
Keyword(s):  
Case Report ◽  
Urinary Tract ◽  
Spina Bifida ◽  
Congenital Scoliosis ◽  
Definite Diagnosis ◽  
Thoracic Cage ◽  
Urinary Tract Abnormalities ◽  
Renal Ectopia ◽  
Crossed Renal Ectopia ◽  
The Right

Introduction: Supernumerary nipples are common anomalies which may be associated with several systemic disorders, particularly urinary tract abnormalities.   Case report: Here we report a case of a 4½ year old male presenting to the pediatric out patient clinic with fever for three days and recurrent sinopulmonary infections. The child had supernumerary nipples over the right side with deformed thoracic cage, congenital scoliosis, diastematomyelia, crossed renal ectopia, and spina bifida. All the conditions present together did not match any syndrome reported till date.   Conclusion: This was a rare syndrome and did not match fully with any known syndromes till date. This case warranted further investigation for its definite diagnosis but we do not have resources to that extent.

scholarly journals Uretero-transappendix-cystoneostomy as a technique for the reconstruction of the lower part of the ureter

2005 ◽  
Vol 62 (12) ◽  
pp. 931-933
Author(s):  
Novak Milovic ◽  
Pero Janjic ◽  
Vladimir Bancevic ◽  
Srdjan Kupresanin
Keyword(s):  
Renal Function ◽  
Case Report ◽  
Surgical Techniques ◽  
Large Defect ◽  
Boari Flap ◽  
Gun Shot ◽  
Psoas Hitch ◽  
The Right

Background. Any large missing part of the ureter may be replaced by transureteroureterostomy, psoas hitch, Boari flap, nephrectomy, renal autotransplanation or by the implementation of an intestinal graft. Case report. A patient with a defect of the lumbal- pelvic portion of the right ureter, after the management of a penetrating and perforating gun shot wound was presented. The missing part of the ureter was successfully replaced with an appendix. The technique of uretero-transappendixcystoneostomy complete with a Boari flap and a psoas hitch was used. Conclusion. By the use of an original combination of surgical techniques, a large defect of the ureter and the defect of the bladder, as well as the preservation of the renal function was achieved in a more successful manner.

A Large Calculus in Crossed Renal Ectopia without Fusion: A Case Report

2013 ◽  
Vol 06 (05) ◽  
Author(s):  
Atul Kumar Khandelwal ◽  
Ahsan Ahmad ◽  
Mahendra Singh ◽  
Vijoy Kumar ◽  
Rajesh Tiwari ◽  
...  
Keyword(s):  
Case Report ◽  
Renal Ectopia ◽  
Crossed Renal Ectopia

scholarly journals Abdominal aortic aneurysm associated with crossed renal ectopia without fusion: Case report and literature review

2003 ◽  
Vol 37 (5) ◽  
pp. 1098-1102 ◽  
Author(s):  
Hiromi Yano ◽  
Naoki Konagai ◽  
Mitsunori Maeda ◽  
Mikihiko Itoh ◽  
Atsushi Kuwabara ◽  
...  
Keyword(s):  
Abdominal Aortic Aneurysm ◽  
Case Report ◽  
Aortic Aneurysm ◽  
Literature Review ◽  
Renal Ectopia ◽  
Abdominal Aortic ◽  
Crossed Renal Ectopia

scholarly journals Synchronous Bilateral Ureteric Metastases as the Presenting Manifestation of Gastric Cancer

2020 ◽  
Vol 2 (5) ◽  
Author(s):  
Swei H. Tsung
Keyword(s):  
Gastric Cancer ◽  
Renal Function ◽  
Gastric Carcinoma ◽  
Computer Tomography ◽  
Immunohistochemical Staining ◽  
Impaired Renal Function ◽  
Final Diagnosis ◽  
Flank Pain ◽  
Medical Attention ◽  
The Right

A 55-year-old man sought medical attention because of the right flank pain. He was anemic with impaired renal function and was admitted to the hospital. Computer tomography demonstrated bilateral hydronephrosis due to ureteral obstruction. Biopsy of both ureters and immunohistochemical staining led to the final diagnosis of gastric carcinoma metastasizing to both ureters. This article presented a case in which metastases of the ureters were the first and sole presentation of gastric cancer.

scholarly journals A Rare Entity in Cushing’s Disease: Severe Hypokalemia and Metabolic Alkalosis

2021 ◽  
Vol 8 (3) ◽  
pp. 189-192
Author(s):  
Seda Turgut ◽  
Muzaffer Ilhan ◽  
Rabia Soytas ◽  
Murat Alay ◽  
Rumeyza Kazancioglu
Keyword(s):  
Case Report ◽  
Cushing’S Disease ◽  
Metabolic Alkalosis ◽  
Final Diagnosis ◽  
University Hospital ◽  
Cushing's Disease ◽  
Resonance Imaging ◽  
Right Lobe ◽  
The Right ◽  
Severe Weakness

Introduction: This case report aimed to highlight the prominence of considering Cushing's disease in the differential diagnosis of severe hypokalemia and metabolic alkalosis. Case Report: A 63-year-old woman who admitted to the emergency room of Bezmialem Vakif University Hospital, Istanbul with fatigue and severe weakness of extremities. Biochemistry results indicated severe hypokalemia (potassium=1.2 mmol/L) and metabolic alkalosis (pH= 7.83) and based on further endocrinological investigations, the final diagnosis of Cushing’s disease was confirmed, and magnetic resonance imaging revealed a macroadenoma in the right lobe of the pituitary. Transsphenoidal surgery was performed and Cushing’s disease was cured without any treatment. Conclusions: Although hypokalemia can be present in Cushing’s disease, none of the previous studies have reported hypokalemia as severe as in this case.

scholarly journals Ureteral triplication: A case report

2005 ◽  
Vol 58 (11-12) ◽  
pp. 592-595 ◽  
Author(s):  
Dragana Zivkovic ◽  
Jan Varga ◽  
Slobodan Grebeldinger ◽  
Vladimir Borisev
Keyword(s):  
Case Report ◽  
Vesicoureteral Reflux ◽  
Clinical Examination ◽  
Excretory Urography ◽  
Fifth Grade ◽  
Ureteral Duplication ◽  
Urinary Infections ◽  
Ureteric Orifice ◽  
Mesonephric Duct ◽  
The Right

Introduction Of all children born with congenital anomalies, 30-40% have urogenital abnormalities. Most of them are asymptomatic, but if any symptoms occur, they are usually symptoms of urinary infections. Case report A four-year old girl was admitted because of recurrent urinary infections and in order to perform a thorough clinical examination. Clinical examination showed an asymmetrical glutens and presence of a fibroma in the same region. Detailed radiologic examinations (ultrasonography, plain X-ray, excretory urography, voiding urethrocystography) revealed a triplicate ureter on the right side with a vesicoureteral reflux of the fifth grade on the same side. Intraoperatively, type III ureteric triplication according to Smith's classification was established. Ureteral remodeling and reimplantation was done. The postoperative course was good, and follow-up voiding urethrocystography showed absence of reflux. Discussion Ureteral triplication is a consequence of either development of three buds on the mesonephric duct, or development of two buds, one of which further divided into two parts. Most common anomalies associated with ureteral triplication are: ureteral duplication on the other side (37%), ectopy of the ureteric orifice (28%) and kidney dysplasia (8%). Vesicoureteral reflux is very common on affected or on both sides. Symptomatology is the same as in ureteral duplication - dominated by signs of urinary infections. Conclusion Diagnosis of ureteral duplication requires detailed imaging. Treatment of symptomatic abnormalities should be individual, regardless of the applied treatment (conservative or operative).

Adolescent Renomedullary Interstitial Cell Tumor: A Case Report

2005 ◽  
Vol 91 (6) ◽  
pp. 555-557 ◽  
Author(s):  
Koray Agras ◽  
Altug Tuncel ◽  
Yilmaz Asian ◽  
Sezer Kulacoglu ◽  
Ali Atan
Keyword(s):  
Case Report ◽  
Interstitial Cell ◽  
Histopathological Examination ◽  
Contrast Material ◽  
Cell Tumor ◽  
Lumbar Region ◽  
Gross Hematuria ◽  
Abdominal Ultrasonography ◽  
Small Tumor ◽  
The Right

A 14-year-old boy presented with painless gross hematuria after a blunt trauma to his right lumbar region. Abdominal ultrasonography and abdominal computerized tomography revealed that the right kidney was hydronephrotic; contrast material delineated a hematoma inside the kidney. The patient underwent a right simple nephrectomy and after histopathological examination was found to have a renomedullary interstitial cell tumor of the right kidney. This tumor is common in patients older than 50 years, whereas our patient was very young. The diagnosis of this small tumor is not possible by conventional radiological techniques and histopathological examination is mandatory for its diagnosis.

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