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Kidney anatomy
 
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Acute nephritic syndrome

Alternative names:

acute glomerulonephritis; glomerulonephritis - acute; nephritis syndrome - acute

Definition:

A group of disorders that cause inflammation of the internal kidney structures (specifically, the glomeruli).

Causes, incidence, and risk factors:

Acute nephritic syndrome is the result of inflammation of the internal structures of the kidney, often caused by unknown factors (such as seen in Henoch-Schonlein prupura) or an immune response triggered by infection or disease (typified by acute post-streptococcal glomerulonephritis).

Despite the diversity of diseases listed below, they share many symptoms in common. Frequently observed symptoms and signs include changes in urine volume (decreased), protein in urine (protinuria), microscopic or gross blood in urine (hematuria), swelling (edema), high blood pressure (hypertension) and a decreased ability of the kidney to remove wastes effectively.

Associated diseases generally seen more frequently in children and adolescents:

Associated diseases generally seen more frequently in adults:

Inflammation disrupts the functioning of the glomerulus, which is the part of the kidney that controls filtering and excretion. Inefficient glomerular functioning results in the loss of blood and protein in the urine and the accumulation of excess fluid in the body. Swelling results when protein is lost from the blood stream. (Protein maintains fluid within the blood vessels, and when it is lost the fluid collects in the tissues of the body).

Urine discoloration results from blood in the urine. This occurs because of loss of blood within the damaged glomeruli.

Acute nephritic syndrome may be associated with the development of hypertension, interstitial inflammation (inflammation of the spaces between the cells of the kidney tissue), and acute renal failure.

The disorder is uncommon, affecting 4 out of 100,000 persons. It affects both sexes and is evenly distributed across age groups.


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