Right lump kidney with varied vasculature and urinary system revealed by multidetector computed tomographic (MDCT) angiography
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  • 作者:Gratian D. Miclaus ; Gheorghe Pupca ; Abigail Gabriel…
  • 关键词:Crossed fused ectopia ; Lump kidney ; Duplex collecting systems ; Renal arteries ; Renal veins ; Variations
  • 刊名:Surgical and Radiologic Anatomy
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:37
  • 期:7
  • 页码:859-865
  • 全文大小:1,638 KB
  • 参考文献:1.Bauer SB (2002) Anomalies of the upper urinary tract. In: Walsh PC, Retik AB, Vaughan ED, Wein AJ (eds) Campbell鈥檚 urology, 8th edn. WB Saunders, Philadelphia, pp 1898鈥?906
    2.Bisset GS 3rd, Strife JL (1987) The duplex collecting system in girls with urinary tract infection: prevalence and significance. AJR Am J Roentgenol 148(3):497鈥?00View Article PubMed
    3.Carleton A (1937) Crossed ectopia of the kidney and its possible cause. J Anat 71(Pt 2):292鈥?98PubMed Central PubMed
    4.Kara E, Ozt眉rk NC, Ozg眉r A, Y谋ld谋z A, Ozt眉rk H (2011) Ectopic kidney with varied vasculature: demonstrated by CT angiography. Surg Radiol Anat 33(1):81鈥?4View Article PubMed
    5.Kaufman MH, Findlater GS (2001) An unusual case of complete renal fusion giving rise to a 鈥榗ake鈥?or 鈥榣ump鈥?kidney. J Anat 198:501鈥?04PubMed Central View Article PubMed
    6.McDonald JH, McClellan DS (1957) Crossed renal ectopia. Am J Surg 93:995鈥?99View Article PubMed
    7.Mekeel KL, Daley SM, Andrews PE, Moss AA, Heilman RL, Mazur MJ, Chakkera HA, Hamawi K, Mulligan DC, Sudhakar Reddy K (2010) Successful transplantation of a split crossed fused ectopic kidney into a patient with end-stage renal disease. J Transplant 2010:383972PubMed Central View Article PubMed
    8.Miclaus GD, Matusz P (2012) Bilateral quadruple renal arteries. Clin Anat 25(8):973鈥?76View Article PubMed
    9.Rinat C, Farkas A, Frishberg Y (2001) Familial inheritance of crossed fused renal ectopia. Pediatr Nephrol 16:269鈥?70View Article PubMed
    10.T眉rkvatan A, Demir D, Ol莽er T, Cumhur T (2006) Cake kidney: MDCT urography for diagnosis. Clin Imaging 30(6):420鈥?22View Article PubMed
    11.Wilmer HA (1938) Unilateral fused kidney: a report of five cases and a review of the literature. J Urol 40:551鈥?71
  • 作者单位:Gratian D. Miclaus (1) (2)
    Gheorghe Pupca (3)
    Abigail Gabriel (4) (5)
    Petru Matusz (1)
    Marios Loukas (4) (6)

    1. Department of Anatomy, 鈥淰ictor Babes鈥?University of Medicine and Pharmacy, 2, Eftimie Murgu Square, 300041, Timisoara, Romania
    2. Neuromed Diagnostic Imaging Centre, Timisoara, Romania
    3. Department of Urology, 鈥淰ictor Babes鈥?University of Medicine and Pharmacy, Timisoara, Romania
    4. Department of Anatomical Sciences, School of Medicine, St. George鈥檚 University, Grenada, West Indies
    5. Department of Internal Medicine, Harlem Hospital Center New York, New York, NY, USA
    6. Department of Anatomy, Medical School Varmia and Mazuria, Olsztyn, Poland
  • 刊物主题:Imaging / Radiology; Orthopedics; Anatomy;
  • 出版者:Springer Paris
  • ISSN:1279-8517
文摘
Renal ectopia also known as ectopic kidney is an embryological renal anomaly characterised by abnormal anatomical location of one or both of the kidneys. This can occur in various forms such as (1) crossed fused renal ectopia, (2) ectopic thoracic kidney and (3) pelvic kidneys. The lump kidney is one of the six variations of crossed fused ectopic kidney. Throughout life, the patient may remain asymptomatic, however, symptomatic patients may present with minor traumatic injuries due to the abnormal location or normal kidney pathologies. During normal embryological development, there is cephalic migration during which the kidneys ascend to their normal retroperitoneal location; therefore, an ectopic location is as a result of arrested migration. During this embryological development the kidney has multiple aorto-illiac branches, which degenerate when the kidney reaches its normal location. Here they develop new renal branches from the aorta and during an arrested ascent the ectopic kidney tends to retain some of the older aorto-iliac vessels. Hence, the arterial supply and the veineux drainage are grossly abnormal, reflecting the metanephric malascent and the primitive vascular arrangement. The collecting systems also present with important anatomical variations. We present an extremely rare case of right lump kidney with six renal arteries, two renal veins and two duplicated pelvicalyceal systems.

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