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  2. Polycystic liver disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_liver_disease

    Polycystic liver disease (PLD) usually describes the presence of multiple cysts scattered throughout normal liver tissue. [1] PLD is commonly seen in association with autosomal-dominant polycystic kidney disease , with a prevalence of 1 in 400 to 1000, and accounts for 8–10% of all cases of end-stage renal disease . [ 2 ]

  3. Autosomal dominant polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Chronic pain in patients with ADPKD is often refractory to conservative, noninvasive treatments, but nonopioid analgesics and conservative interventions can be first used before opioid analgesics are considered; if pain continues, then surgical interventions can target renal or hepatic cysts to directly address the cause of pain, with surgical ...

  4. 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] Cysts ...

  5. Autosomal recessive polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_recessive...

    In a typical presentation, a small number of individuals with ARPKD live to adulthood with some kidney function; but with significant deterioration in liver function. [8] This outcome is postulated to result from expression of the polycystic kidney and hepatic disease gene PKHD1, which is located on chromosome 6p. [9]

  6. Cystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Cystic_kidney_disease

    Cystic kidney disease includes various conditions related to the formation of cysts in one or both kidneys. The most common subset is polycystic kidney disease (PKD), which is a genetic anomaly with two subsets, autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD).

  7. Kidney disease - Wikipedia

    en.wikipedia.org/wiki/Kidney_disease

    These cysts become enlarged with the progression of aging causing renal failure. Cysts may also form in other organs including the liver, brain, and ovaries. Polycystic kidney disease is a genetic disease caused by mutations in the PKD1, PKD2, and PKHD1 genes. This disease affects about half a million people in the US.

  8. Liver tumor - Wikipedia

    en.wikipedia.org/wiki/Liver_tumor

    Simple liver cysts are seen most commonly in women and kids. [2] In terms of pathophysiology, they are formed in response to developmental events and in response to trauma and inflammation. [2] In addition, liver cysts can be seen with polycystic kidney disease and echinococcosis infection (hydatid disease). [2] [12] Pseudotumors:

  9. Renal cyst - Wikipedia

    en.wikipedia.org/wiki/Renal_cyst

    A renal cyst is a fluid collection in or on the kidney. There are several types based on the Bosniak classification. There are several types based on the Bosniak classification. The majority are benign, simple cysts that can be monitored and not intervened upon.