A rare case of ureteropelvic junction obstruction by an aberrant renal vessels
نویسندگان
چکیده
منابع مشابه
A Rare Cause of Ureteropelvic Junction Obstruction
An 8-year-old boy was referred to Pusan National University Yangsan Hospital with left ureteropelvic junction (UPJ) obstruction. He had experienced episodes of intermittent gross hematuria that had first presented at the age of 5 years. He was otherwise healthy and had no previous medical problems. He had no history of urinary tract infections or stones. A physical examination showed no left fl...
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Ureteropelvic junction UPJ obstruction is caused by the presence of an aperistaltic dysplastic segment at the UPJ. Besides this intrinsic etiology, extrinsic factors, mainly crossing vessels, maybe the causative factor. The controversy regarding the functional significance of vessels crossing at the UPJ is not a new one, though this debate has been resurrected in recent years because of improve...
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This case report describes a distal ureteral atresia along with ureteropelvic junction obstruction which occurred in a 19-month-old female child. It is easily to be misdiagnosed as mere ureteropelvic junction obstruction and omitted the combined diagnosis of distal ureteral atresia. Dismembered pyeloplasty was done in local hospital after admission, however with the result of recurrent fever wh...
متن کاملDouble Trouble: A Rare Case of Bilateral Upper Pole Ureteropelvic Junction Obstruction☆
A 16-year-old girl presented with bilateral back pain caused by bilateral upper pole ureteropelvic junction obstructions; an extremely rare phenomenon. Bilateral robotically assisted upper pole pyeloplasties were preformed at the same setting with an excellent clinical response. Although rare, upper pole ureteropelvic junction obstruction is a defined entity that urologists should be aware of.
متن کاملRenal osteodystrophy secondary to congenital bilateral ureteropelvic junction obstruction.
A 4-year-old girl presented with progressive distension of the abdomen and bowing of the legs (genu valgum) since birth. She was anemic, with a blood pressure of 180/110 mmHg. The serum level of creatinine was 1.7 mg/dL. She had hypocalcemia, and elevated serum level of phosphorous and parathyroid hormones. Ultrasonography revealed bilateral grossly hydronephrotic kidneys with thinned out paren...
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ژورنال
عنوان ژورنال: International Journal of Surgery Science
سال: 2020
ISSN: 2616-3462,2616-3470
DOI: 10.33545/surgery.2020.v4.i2c.412