Isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis is a medical condition that affects the kidneys. It is a rare condition that occurs when the immune system attacks the glomeruli, which are the small blood vessels in the kidneys that filter waste and excess fluid from the blood. When these blood vessels become inflamed, they can leak protein into the urine, leading to isolated proteinuria.
The condition is called "isolated" proteinuria because it typically occurs without any other signs of kidney damage. Patients with isolated proteinuria may not experience any pain or discomfort, and their kidneys may continue to function normally for some time.
However, if left untreated, isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis can progress to more severe forms of glomerulonephritis, which can cause kidney damage and eventually lead to kidney failure.
The symptoms of isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis can vary from person to person. Some patients may not experience any symptoms at all, while others may experience mild to severe symptoms such as:
If you are experiencing any of these symptoms, it is important to see a doctor right away. They can perform a blood or urine test to diagnose isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis.
The exact cause of isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis is not fully understood. However, it is believed to be an autoimmune disorder, meaning that the body's immune system mistakenly attacks healthy tissue in the kidneys.
Other factors that may contribute to the development of isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis include:
If you have a family history of kidney disease or autoimmune disorders, you may be at a higher risk of developing isolated proteinuria with
To see full information about treatment please Sign up or Log in