scholarly journals Multicystic Left Kidney and Contralateral Pelvic Kidney with Ectopic Ureter and Renal Failure in a Young Male: A Rare Association

Author(s):  
Pritesh Jain ◽  
Debansu Sarkar ◽  
Dilip Kumar Pal
1985 ◽  
Vol 68 (1) ◽  
pp. 15-21 ◽  
Author(s):  
A. M. El Nahas ◽  
R. Lechler ◽  
S. N. Zoob ◽  
A. J. Rees

1. We studied the relation between immunopathology and progressive renal failure after nephrotoxic nephritis (NTN) in rats. 2. Thirty days after induction of nephritis by injection of rabbit anti-rat nephrotoxic serum, pairs of kidneys from 13 nephritic rats were transplanted into separate syngeneic recipients, one of whom had been pre-immunized with rabbit immunoglobulin G (IgG) whilst the other was naive. 3. Progression to renal failure of the transplanted nephritic kidney was studied after removal of the recipient's own kidneys; results from right and left kidney from a single donor in pre-immunized and naive recipients were compared. 4. There were substantial differences in autologous anti-rabbit IgG titres in naive and pre-immunized recipients; despite this pairs of kidneys from the same donor had almost identical courses as assessed by proteinuria, serum creatinine and graft survival. 5. There was substantial variation in survival of kidneys from different donors. But there were very strong correlations of graft survival with proteinuria (r = 0.97, t = 4.443, P<0.001) and reciprocal serum creatinine (r = 0.95, t = 4.32, P<0.001) in donors shortly before transplantation. 6. We conclude that autologous antibody titres did not influence the progression to renal failure after nephrotoxic nephritis. The rate of progression was already determined at the time of transplantation.


Ultrasound ◽  
2009 ◽  
Vol 17 (2) ◽  
pp. 90-92
Author(s):  
Andrew Christie

This case represents an incidental splenic cyst misinterpreted as a supernumerary kidney, resulting in a computed tomography scan to confirm the ultrasound (US) findings. A 55-year-old man presenting with renal failure had an US examination which showed a mass adjacent to the left kidney. It resembled a kidney with a dilated collecting system rather than a spleen. Supernumerary kidneys are extremely rare in the published literature. Splenic cysts are more common, but are still relatively unusual. The possible diagnoses and US findings in splenic cysts are discussed.


2000 ◽  
Vol 3 (5) ◽  
pp. 472-478 ◽  
Author(s):  
Keshani de Silva ◽  
Vivienne Tobias ◽  
Gad Kainer ◽  
Bruce Beckwith

We report a case of a 9-year-old boy with focal, segmental glomerulosclerosis who, following peritoneal dialysis, underwent renal transplantation and bilateral nephrectomy. The kidneys showed histological features of embryonal hyperplasia of Bowman's capsular epithelium, an uncommon lesion that is seen most often in patients with chronic renal failure who are being maintained on dialysis. In addition, a 1-cm tumor in the left kidney showed features of metanephric adenoma. Although both lesions are uncommon, they share many similarities on a morphological, immunohistochemical, and ultrastructural basis. This association has not been previously reported and may shed some light on the histogenesis of these recently described lesions.


1998 ◽  
Vol 33 (11) ◽  
pp. 1731-1732 ◽  
Author(s):  
W.T.Ng Jacob ◽  
C.K Yeung ◽  
Kelvin K.W Liu

Author(s):  
Christine U. Lee ◽  
James F. Glockner

85-year-old man with acute on chronic renal failure Coronal SSFSE (Figure 7.8.1), axial FSE (Figure 7.8.2), and axial diffusion-weighted (b=100 s/mm2) (Figure 7.8.3) images reveal a small left kidney with hydronephrosis of upper pole calyces. Nodular thickening involves the renal capsule and Gerota fascia, with larger nodules adjacent to the renal hilum and within the perinephric fat. Note also the right-sided renal cysts....


2015 ◽  
Vol 76 (1) ◽  
Author(s):  
Cinzia Perrino ◽  
Laura Scudiero ◽  
Maria Piera Petretta ◽  
Gabriele Giacomo Schiattarella ◽  
Mario De Laurentis ◽  
...  

Total occlusion of the abdominal aorta is unusual, and potentially catastrophic. It occurs in patients with advanced atherosclerotic occlusive disease, and can cause severe ischemic manifestations, depending on the site of obstruction. Prompt and appropriate diagnostic and therapeutic approaches are important whenever this condition is suspected, in order to avoid a fatal outcome. The development of a complex network of collaterals may prevent the manifestation of acute ischemic phenomena, and cause a delay in diagnosis and treatment. Here we report the clinical case of a 59-year-old man who was referred to our Department for evaluation of renal failure and refractory hypertension. Ultrasonography and 99mTc-DTPA scintigraphy showed a shrunken, non-functioning left kidney, while CT angiography and aortography showed the complete occlusion of the aorta from below the right renal artery down to the bifurcation of both common iliac arteries, with a critical stenosis of the origin of the right renal artery, an occlusion of the left renal artery as well as of the origin of the inferior mesenteric artery. The patient was referred to the surgery department for aorto-bifemoral bypass surgery and re-implantation of the right renal artery.


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