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renal cyst
Renal cell carcinoma presenting as a huge simple renal cyst
      
Transformation of a simple renal cyst into a renal cell carcinoma (RCC), however, is extremely rare.
      
We reported a 48-year-old man with a right huge simple renal cyst from which about 800?ml of dark yellowish fluid with elevated protein and lactic dehydrogenase (LDH) levels was aspirated.
      
e., renal biopsy, renal cyst resections, ureterocutaneostomy) and 102 as difficult (i.e.
      
Two cases of haemorragic renal cyst presenting in the neonatal period are described.
      
Usually, renal calcification in patients with autosomal dominant polycystic kidney disease is manifested as calculi or as hemorrhage into a renal cyst.
      
Percutaneous sclerotherapy of a symptomatic simple renal cyst in a child: observation of membrane detachment sign
      
A 6-year-old girl with 21 sy mptomatic renal cyst underwent successful percutaneous aspiration and sclerotherapy with hypertnic saline under US guidance.
      
Therefore differntiation of a symptomatic renal cyst from a hydatid cyst should not depend solely on membrane detachmentIn either case US- or CT-guided percutatneous sclerotherapy should always be considered before surgery.
      
Biopsy revealed 15 benign diagnoses: oncocytoma (n=6), hemorrhagic renal cyst (n=3), chronic nephritis (n=3), angiomyolipoma (n=2), and mycotic renal abscess (n=1).
      
Multilocular renal cyst is an uncommon focal, unilateral, cystic, epithelial lesion of uncertain pathogenesis.
      
In the case of this lesion, the distinction between a benign and a malignant renal cyst is blurred.
      
The main pathology is from renal cyst formation that eventually leads to end-stage renal failure during adult life.
      
Other studies have yielded new information regarding the role of the epidermal growth factor receptor gene in promoting renal cyst formation.
      
Chronic hypokalemia is known to induce renal cyst formation in some diseases including primary aldosteronism, distal renal tubular acidosis, Liddle disease and apparent mineralocorticoid excess syndrome.
      
Although chronic hypokalemia is the main clinical feature of Bartter syndrome, renal cyst formation in this disease has never been reported.
      
Renal cyst development in polycystic kidney disease (PKD) involves hyperplastic growth and extensive membrane alterations, suggesting abnormal membrane composition and function.
      
At sacrifice, kidneys frompcy mice were four times larger than DBA controls, indicating that extensive renal cyst growth had occurred.
      
In this patients, echography revealed a renal cyst containing a stone.
      
Residual contrast medium in the cortex of the kidney around an infected renal cyst on CT: case report
      
 

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