Lupus nephritis: Difference between revisions
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{{Infobox_Disease | | {{Infobox_Disease | | ||
Name = Lupus nephritis | | Name = Lupus nephritis | | ||
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==Classification== | ==Classification== | ||
The World Health Organization has divided lupus nephritis into five classes based on the biopsy. | The World Health Organization has divided lupus nephritis into five classes based on the [[biopsy]]. | ||
*Class I is histologically normal and does not show any evidence of disease. | *Class I is histologically normal and does not show any evidence of disease. | ||
*Class II is based on a finding of mesangial lupus nephritis | *Class II is based on a finding of mesangial lupus nephritis | ||
*Class III is focal proliferative nephritis | *Class III is focal proliferative [[nephritis]] | ||
*Class IV is diffuse proliferative nephritis | *Class IV is diffuse proliferative nephritis | ||
*Class V is membranous nephritis and is characterized by extreme edema and protein loss. | *Class V is membranous nephritis and is characterized by extreme edema and protein loss. | ||
*Class VI Glomerulosclerosis | *Class VI Glomerulosclerosis | ||
==Pathophysiology== | |||
Systemic lupus erythematosus (SLE, or lupus) is an [[autoimmune]] disease. This means there is a problem with the body's immune system. | |||
Normally, the immune system helps protect the body from harmful substances. But in patients with an autoimmune disease, the immune system cannot tell the difference between harmful substances and healthy ones. As a result, the immune system attacks otherwise healthy cells and tissue. | |||
==Differentiating from other Diseases== | |||
Diseases with similar symptoms are | |||
* [[Chronic glomerulonephritis]] | |||
* [[Polyarteritis nodosa]] | |||
* [[Wegener granulomatosis ]] | |||
==Natural History, Complications and Prognosis== | |||
* [[Lupus nephritis]] may damage different parts of the kidney. Class I has normal histology and does not show any evidence of disease and class V shows an extensive disease. | |||
* Possible complications include: | |||
** Interstitial nephritis | |||
** [[Nephrotic syndrome]] | |||
** [[Membranous glomerulonephritis]] | |||
** [[Kidney failure]] | |||
==Diagnosis== | ==Diagnosis== | ||
===Symptoms=== | ===Symptoms=== | ||
Sufferers of lupus nephritis may or may not have symptoms of [[kidney disease]], but it can manifest itself through | Sufferers of lupus nephritis may or may not have symptoms of [[kidney disease]], but it can manifest itself through: | ||
* [[Weight gain]] | |||
* [[Hypertension|high blood pressure]] | |||
* Darker foamy [[urine]] | |||
* [[Edema|swelling]] around the eyes, legs, ankles or fingers. | |||
Furthermore, patients may suffer from other symptoms of lupus unrelated to kidney function. Such symptoms can include [[ | Furthermore, patients may suffer from other symptoms of lupus unrelated to kidney function. Such symptoms can include | ||
* [[Arthritis]] | |||
* [[Fevers]] | |||
* Gastro-intenstinal disturbances | |||
* [[Headaches]] | |||
* [[Fatigue (physical)|Fatigue]] | |||
* Swollen joints Fluid in the joints. | |||
===Physical Examination=== | |||
====Skin==== | |||
The diagnosis of lupus nephritis depends on [[blood]] tests, [[urinalysis]], X-rays, [[ultrasound]] scans of the kidneys, and a kidney [[biopsy]]. | The diagnosis of lupus nephritis depends on [[blood]] tests, [[urinalysis]], X-rays, [[ultrasound]] scans of the kidneys, and a kidney [[biopsy]]. |
Revision as of 14:11, 3 August 2012
Lupus nephritis | |
Type IV lupus nephritis: The classic "flea-bitten" appearance of the cortical surface in the diffuse proliferative glomerulonephritides. (Courtesy of Ed Uthman, MD)]] | |
ICD-10 | N08.5 |
ICD-9 | 583.81 |
MedlinePlus | 000481 |
MeSH | D008181 |
For patient information, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2] Ujjwal Rastogi, MBBS [3]; Raviteja Guddeti, M.B.B.S. [4]
Overview
Lupus nephritis is an inflammation of the kidney caused by systemic lupus erythematosus (SLE), a disease of the immune system. Apart from the kidneys, SLE can also damage the skin, joints, nervous system and virtually any organ or system in the body.
Classification
The World Health Organization has divided lupus nephritis into five classes based on the biopsy.
- Class I is histologically normal and does not show any evidence of disease.
- Class II is based on a finding of mesangial lupus nephritis
- Class III is focal proliferative nephritis
- Class IV is diffuse proliferative nephritis
- Class V is membranous nephritis and is characterized by extreme edema and protein loss.
- Class VI Glomerulosclerosis
Pathophysiology
Systemic lupus erythematosus (SLE, or lupus) is an autoimmune disease. This means there is a problem with the body's immune system.
Normally, the immune system helps protect the body from harmful substances. But in patients with an autoimmune disease, the immune system cannot tell the difference between harmful substances and healthy ones. As a result, the immune system attacks otherwise healthy cells and tissue.
Differentiating from other Diseases
Diseases with similar symptoms are
Natural History, Complications and Prognosis
- Lupus nephritis may damage different parts of the kidney. Class I has normal histology and does not show any evidence of disease and class V shows an extensive disease.
- Possible complications include:
- Interstitial nephritis
- Nephrotic syndrome
- Membranous glomerulonephritis
- Kidney failure
Diagnosis
Symptoms
Sufferers of lupus nephritis may or may not have symptoms of kidney disease, but it can manifest itself through:
- Weight gain
- high blood pressure
- Darker foamy urine
- swelling around the eyes, legs, ankles or fingers.
Furthermore, patients may suffer from other symptoms of lupus unrelated to kidney function. Such symptoms can include
- Arthritis
- Fevers
- Gastro-intenstinal disturbances
- Headaches
- Fatigue
- Swollen joints Fluid in the joints.
Physical Examination
Skin
The diagnosis of lupus nephritis depends on blood tests, urinalysis, X-rays, ultrasound scans of the kidneys, and a kidney biopsy. Medicines which decrease swelling, lower blood pressure and decrease inflammation by suppressing the immune system. Patients may need to monitor intake of protein, sodium, and potassium. Patients with severe disease should restrict their sodium intake to 2 grams per day and limit fluid as well. Depending on the histology, renal function and degree of proteinuria, patients may require steroid therapy or chemotherapy regimens such as cyclophosphamide, azathioprine, mycophenolate mofetil or cyclosporine.
The medical therapy for lupus nephritis depends on the severity of the disease. For mild disease, corticosteroids are generally prescribed. More severe disease requires treatment with immunosuppressant agents. The two most commonly used agents are mycophenolate mofetil and intravenous cyclophosphamide. One recent study compared these two drugs.[1] The authors showed that patients with Class III or IV disease are more likely to benefit from mycophenolate mofetil as compared to cyclophosphamide. As a result, mycophenolate mofetil is now considered to be the first-line therapy for this disease.
References
- ↑ Ginzler EM, Dooley MA, Aranow C, Kim MY, et al. "Mycophenolate Mofetil or Intravenous Cyclophosphamide for Lupus Nephritis." New England Journal of Medicine. 353:21. 2219-2229. 24 November 2005.
External links
- Lupus Nephritis Clinical Research Study
- London Lupus Centre - Treatment, Diagnosis, Research
- Lupus Foundation of America, Inc.
- Lupus Research Institute
- S.L.E. Lupus Foundation
- Lupus International