Nephritic syndrome
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| Nephritic syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | N00, N01, N03, N05 |
| ICD-9-CM | 580 |
| MedlinePlus | 000495 |
| Patient UK | Nephritic syndrome |
Nephritic syndrome (or acute nephritic syndrome)[1] is a collection of signs (known as a syndrome) associated with disorders affecting the kidneys, more specifically glomerular disorders.[2] It is characterized by having a thin glomerular basement membrane and small pores in the podocytes of the glomerulus, large enough to permit proteins (proteinuria) and red blood cells (hematuria) to pass into the urine. By contrast, nephrotic syndrome is characterized by only proteins moving into the urine. Nephritic syndrome, like nephrotic syndrome, may involve hypoalbuminemia due to protein albumin moving from the blood to the urine.[medical citation needed]
Contents
Signs and symptoms
Symptoms consistent with nephritic syndrome are:
- Hematuria (blood in the urine)[3]
- Proteinuria (protein in the urine)[3]
- Hypertension[4]
- Blurred vision[5]
- Azotemia[6]
- Oliguria (low urine output <400 mL/day)[6]
Cause
Nephritic syndrome is caused by inflammation of glomerulus and has urine waste, furthermore the cause can be infectious, autoimmune or thrombotic.[7] The causes can be divided between age groups as follows:[5]
Children/Adolescents
- IgA nephropathy
- Post-streptococcal glomerulonephritis
- Hemolytic uremic syndrome
- Henoch-Schoenlein purpura
Adults
Pathophysiology
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.[8]
Diagnosis
The classic diagnoses of nephritic syndrome is post-streptococcal glomerulonephritis,[9] 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.[5]
Treatment
Treatment of nephritic syndrome is consistent with administration of antihypertensives and anti-inflammatory medication. Furthermore, a reduction in potassium (K+) and salt, as well as physical rest.[5]
Prognosis
Because nephritic syndrome is not a disease, the prognosis depends on the underlying etiology. The prognosis of nephritic syndome in children due to post-streptococcal glomerulonephritis is good.[10]
References
- ↑ "acute nephritic syndrome" at Dorland's Medical Dictionary
- ↑ http://www.merck.com/mmpe/sec17/ch235/ch235b.html
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Further reading
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External links
- Nephritic syndrome - A to Z topics.
