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  2. Angiomyolipoma - Wikipedia

    en.wikipedia.org/wiki/Angiomyolipoma

    Angiomyolipoma seen as a hyperechoic mass in the upper pole of an adult kidney on renal ultrasonography. Renal ultrasonography of a person with tuberous sclerosis and multiple angiomyolipomas in the kidney: Measurement of kidney length on the US image is illustrated by '+' and a dashed line. CT scan of a renal angiomyolipoma.

  3. Renal hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Renal_hypoplasia

    Segmental hypoplasia or Ask-Upmark kidney is a rare renal disease where a part of the kidney has undergone hypoplasia. The number of renal lobes is reduced, and the kidney size is less than two standard deviations from the average, with the weight often being over 50g in adults and 12–25g in children.

  4. Renal cyst - Wikipedia

    en.wikipedia.org/wiki/Renal_cyst

    Approximately 40 to 60% of these lesions are ultimately found to be malignant, most commonly in the forms of cystic renal cell carcinoma and its multiloculated variant. [8] [9] [10] The remaining lesions are benign and include hemorrhagic cysts, chronic infected cysts, and multiloculated cystic nephromas.

  5. Focal segmental glomerulosclerosis - Wikipedia

    en.wikipedia.org/wiki/Focal_segmental_glomerulo...

    Signs and symptoms include proteinuria and edema. [ 2 ] [ 5 ] Kidney failure is a common long-term complication of the disease. [ 5 ] [ 6 ] FSGS can be classified as primary, secondary, or genetic, depending on whether a particular toxic or pathologic stressor or genetic predisposition can be identified as the cause.

  6. Renal cell carcinoma - Wikipedia

    en.wikipedia.org/wiki/Renal_cell_carcinoma

    The five-year survival rate was higher for incidental than for symptomatic tumours: 85.3% versus 62.5%. Incidental lesions were significantly lower stage than those that cause symptoms, since 62.1% patients with incidental renal cell carcinoma were observed with Stage I lesions, against 23% were found with symptomatic renal cell carcinoma. [111]

  7. Polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_kidney_disease

    Polycystic kidney disease (PKD or PCKD, also known as polycystic kidney syndrome) is a genetic disorder [5] [6] in which the renal tubules become structurally abnormal, resulting in the development and growth of multiple cysts within the kidney. [7] These cysts may begin to develop in utero, in infancy, in childhood, or in adulthood. [8]

  8. Kidney tumour - Wikipedia

    en.wikipedia.org/wiki/Kidney_tumour

    The RENAL Nephrometry Scoring System is used to measure the complexity of kidney tumors for determining whether a renal mass is appropriate for partial or radical nephrectomy, and is estimated by CT scan as follows: [7] The nephrometery score takes into account the size of the tumor (Radius), how much of the tumor is inside or outside of the ...

  9. Renal ultrasonography - Wikipedia

    en.wikipedia.org/wiki/Renal_ultrasonography

    The kidney is surrounded by a capsule separating the kidney from the echogenic perirenal fat, which is seen as a thin linear structure. [1] The kidney is divided into parenchyma and renal sinus. The renal sinus is hyperechoic and is composed of calyces, the renal pelvis, fat and the major intrarenal vessels.