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 ◽  
...  
2003 ◽  
Vol 37 (5) ◽  
pp. 1098-1102 ◽  
Author(s):  
Hiromi Yano ◽  
Naoki Konagai ◽  
Mitsunori Maeda ◽  
Mikihiko Itoh ◽  
Atsushi Kuwabara ◽  
...  

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 ◽  
...  

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.


2021 ◽  
Vol 6 (1) ◽  
pp. 71-75
Author(s):  
Osama Bani Hani ◽  
Omar Halalsheh ◽  
Yazeed Mohammad ◽  
Anas Bani Yaseen ◽  
Ruba Khasawneh ◽  
...  

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.


PEDIATRICS ◽  
1971 ◽  
Vol 48 (3) ◽  
pp. 454-457
Author(s):  
David T. Mininberg ◽  
Stephanie Roze ◽  
H. J. Yoon ◽  
Marylin Pearl

Hypertension is not found commonly in infants under 1 year of age. Renovascular type of hypertension is extremely rare in this age group. A 3-month-old male infant is presented who developed hypertension secondary to the unilateral anomaly of crossed renal ectopia. This was associated with two other developmental anomalies, imperforate anus Type III-B and rectourethral fistula. The hypertension was treated successfully by surgery. Case Report A male infant, the full-term product of a 34-year-old G6P4A1 mother, was born by normal spontaneous delivery, weighing 5 pounds 8½ ounces. Physical examination was entirely normal except for the presence of an imperforate anus which subsequently proved to be Type III-B.


1989 ◽  
Vol 142 (2 Part 1) ◽  
pp. 366-368 ◽  
Author(s):  
Marc S. Rocklin ◽  
Keith N. Apelgren ◽  
Carol A. Slomski ◽  
Stanley J. Kandzari

2016 ◽  
Vol 3 (2) ◽  
pp. 55
Author(s):  
Kiran Panthee ◽  
Kiran Sharma ◽  
Balkrishna Kalakheti

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.


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