The clinical manifestation of polycystic kidney disease

The disease is slow onset, asymptomatic before the onset, it is clinically visible in many patients in the routine physical examination found to come to medical treatment. Through the family genetic survey often family history, and not generations of inheritance. The clinical symptoms of the age of more than 35-45 years old, an average of 40.7 years old. Clinical symptoms and cysts and damaged kidney tissue two aspects.

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Symptoms associated with cysts are backache, low back pain, bloating, abdominal mass, gross hematuria, acute infection, and colic if blood clots or concurrent stones block the ureter. When the disease progress, renal tissue compression, impaired renal function and chronic renal insufficiency, eventually uremia. In the uremia before the emergence of often due to loss of function of the collection tube caused by reduced renal function, such as low specific gravity urine, urine output increased significantly. About 50% to 75% of patients have high blood pressure. Urine routine examination often red, white blood cells and mild urinary protein.

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In addition, the disease manifested kidney cysts, ovarian cysts, pancreatic cyst symptoms. Common complications of urinary tract infection, urinary tract stones and urinary tract obstruction.

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