Nephritic syndrome

Nephritic syndrome
Classification and external resources
Specialty	urology
ICD-10	N00, N01, N03, N05
ICD-9-CM	580
MedlinePlus	000495
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Nephritic syndrome (or acute nephritic syndrome) is a syndrome comprising signs of nephritis, which is kidney disease involving inflammation. It often occurs in glomerulonephritis, which is characterized by a thin glomerular basement membrane and small pores in the podocytes of the glomerulus, large enough to permit proteins and red blood cells to pass into the urine (yielding proteinuria and hematuria). By contrast, nephrotic syndrome is characterized by only proteins moving into the urine. Nephritic syndrome, like nephrotic syndrome, may involve hypoalbuminemia due to the protein albumin moving from the blood to the urine.

Symptoms consistent with nephritic syndrome are:

Nephritic syndrome is caused by inflammation of glomerulus and has urine waste, furthermore the cause can be infectious, autoimmune or thrombotic. The causes can be divided between age groups as follows:

Children/Adolescents

Adults

The pathophysiology of nephritic syndrome is dependent on where damage is done by antibody-antigen complexes (in glomerulus). In the case of IgA nephropathy, the glomerulus cannot filter IgA antibody-antigen, and this causes an inflammatory response, then release of cytokines (and growth factors), and finally results in glomerular scarring.

The classic diagnoses of nephritic syndrome is , which is a common complication of Streptococcus bacterial infections, typically of the skin.

Among the tests done to diagnose if an individual has nephritic syndrome are: blood electrolytes, blood urea nitrogen, potassium test, protein in the urine, urinalysis and kidney biopsy.

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