Polycystic Kidney Disease (PKD) belongs to hereditary Kidney Disease, kind of
congenital abnormality. Cysts of Polycystic Kidney Disease (PKD) are mainly
caused by eccyliosis of renal parenchyma and renal structure, with different
involvement of each kidney. These cysts compress surrounding healthy renal
tissue, which can cause renal ischemia and anoxia as well as low renal
perfusion. Then Hypertension of Polycystic Kidney Disease (PKD) happens, which
means that Polycystic Kidney Disease (PKD) patients begin to suffer from
Hypertension.
Through observation, many grapelike cysts with different sizes spread over
the whole renal tissue, and the volume of cysts is much larger than the volume
of renal parenchyma. Kidney enlarges obviously and light yellow liquid can be
found in cyst at kidney section. Due to internal bleeding, liquid color may be
red or brown, contenting tiny protein, chloride, cholesterin and light urea.
Cysts may be open to each other, but isolated with renal pelvis. Cystic pressure
on renal tissue can cause renal tubule atrophy and sclerosis, damage glomerulus
and renal function. Besides, these cysts also compress kidney blood vessels,
reducing local blood flow. Therefore, there will be a high concentration of
angiotensin with shrunk blood vessel, leading to Hypertension. In some degree,
it is a vicious circle between Hypertension and renal function injury.
Based on the above, generally, once Polycystic Kidney Disease (PKD) patients
get Hypertension, it means that renal function is about to decline or has
already been damaged. For this reason, patients should pay more attention on
controlling Hypertension.
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