A rare case of supernumerary kidney with crossed fused ectopia kidney
نویسندگان
چکیده
منابع مشابه
A rare case of supernumerary fused and malrotated kidney
The supernumerary kidney is an accessory organ with its own blood supply and collecting system. It is a very rare type of congenital renal anomaly with fewer than 100 cases reported since firstly described at 1656 (1). Embryological basis of supernumerary kidney is connected to the abnormal division of the nephrogenic cord into two metanephric blastemas which will form two kidneys (2). It may b...
متن کاملLaparoscopic heminefrectomy for crossed fused kidney with inferior ectopia.
OBJECTIVES Crossed fused renal ectopia is a rare congenital anomaly. We report the case of a 3 year old boy with diagnosis of right crossed fused renal ectopia, history of recurrent urinary tract infection and previous failure of surgical treatment. METHODS Three year old boy with diagnosis of right crossed fused renal ectopia of the inferior moiety underwent a laparoscopic heminephrectomy of...
متن کاملCrossed Fused Ectopic Kidney: A Case Report.
Crossed fused ectopic kidney is an unusual congenital malformation of the urinary tract. This condition is usually identified in the autopsy specimen rather than in general clinical scenario. In this condition, both kidneys are located on one side of the midline and are fused with each other. This condition is generally asymptomatic and usually diagnosed as incidental finding. We came across a ...
متن کاملFused supernumerary kidney
A partially fused supernumerary kidney with bifid ureters was diagnosed in a 35-year-old female patient using ultrasound and triple-phased computed tomography (CT). The CT also revealed two separate renal arteries supplying each of the left kidney and multiple left renal veins, forming a common trunk to drain into the inferior vena cava. Supernumerary kidney is a rare congenital anomaly; fewer ...
متن کاملA rare association of crossed fused renal ectopia
BACKGROUND Thrombocytopenia and absent radius syndrome (TAR) is a rare genetic disorder. It is an autosomal recessive disorder characterised by radial aplasia and thrombocytopenia that may have additional anomalies. We report a case of TAR syndrome with crossed fused renal ectopia. This anomaly has not been previously reported in association with TAR syndrome. CASE PRESENTATION A 24 years old...
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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.i3d.500