Renal amyloidosis overview: Difference between revisions
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{{Renal Amyloidosis}} | {{Renal Amyloidosis}} | ||
{{CMG}}; {{AE}} | {{CMG}} ; {{AE}} [[User:Okamal|Omer Kamal, M.D.]] [Mailto:okamal@bidmc.harvard.edu| <nowiki>[2]</nowiki>] | ||
==Overview== | ==Overview== | ||
Nicolaus Fontanus was the first to describe [[amyloidosis]] based on the result of an autopsy while Rudolph Virchow was the first to introduce the term [[amyloidosis]]. [[Renal amyloidosis]] can be classified according to the site of [[amyloid]] deposition into glomerular, vascular, and tubular [[amyloidosis]]. Suggested mechanisms of renal involvement include abnormal [[protein]] production or hereditary mutation. If left untreated, [[renal amyloidosis]] may progress into end stage renal disease. Common complications include [[chronic renal failure]] and [[nephrotic syndrome]]. After a few years, [[renal amyloidosis]] eventually leads to end stage renal disease and it may be progressed in presence of certain factors such as steroid administration, [[renal vein thrombosis]], [[Infection|infections]] and [[surgery]]. There is insufficient evidence to recommend routine screening for [[renal amyloidosis]]. Renal biopsy is the gold standard test for the diagnosis of [[Renal amyloidosis|renal diagnosis]]. The mainstay of treatment for renal amyloidosis is to decrease the production or increase clearing of [[amyloid]]. Pharmacologic medical therapies for renal amyloidosis include [[colchicine]], [[azathioprine]], [[Dimethyl sulfoxide|dimethylsulfoxide]], [[chlorambucil]], [[methotrexate]], [[cyclophosphamide]] and TNF-alpha antagonists (ie, [[etanercept]], [[infliximab]], and [[adalimumab]]). | |||
==Historical Perspective== | ==Historical Perspective== | ||
Nicolaus Fontanus was the first to describe [[amyloidosis]] based on the result of an autopsy while Rudolph Virchow was the first to introduce the term [[amyloidosis]]. | |||
==Classification== | ==Classification== | ||
[[Renal amyloidosis]] can be classified according to the site of [[amyloid]] deposition into glomerular, vascular, and tubular [[amyloidosis]]. | |||
Renal amyloidosis | |||
==Pathophysiology== | ==Pathophysiology== | ||
Suggested mechanisms of renal involvement include abnormal [[protein]] production or hereditary mutation. | |||
==Causes== | ==Causes== | ||
Most common causes of renal [[amyloidosis]] include primary and secondary [[amyloidosis]]. Other causes include [[transthyretin]] and [[fibrinogen]] [[amyloid]] deposition. | |||
==Differentiating Renal amyloidosis from Other Diseases== | ==Differentiating Renal amyloidosis from Other Diseases== | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
The [[incidence]] is 97 to 140 cases per 100,000 individuals. The incidence of renal amyloidosis increases with age; the median age at diagnosis is 65 years. | |||
The incidence is | |||
The | |||
==Risk Factors== | ==Risk Factors== | ||
Common risk factors in the development of renal amyloidosis may be environmental and genetic such as heterozygous mutations in the genes for [[lysozyme]], [[Apolipoprotein A1|apolipoprotein AI]], [[Apolipoprotein A2|apolipoprotein AII]], or [[Fibrinogen alpha chain|fibrinogen]] A alpha-chain. | |||
==Screening== | ==Screening== | ||
There is insufficient evidence to recommend routine screening for renal amyloidosis. | There is insufficient evidence to recommend routine screening for [[renal amyloidosis]]. | ||
==Natural History, Complications, and Prognosis== | ==Natural History, Complications, and Prognosis== | ||
If left untreated, [[renal amyloidosis]] may progress into end stage renal disease. Common complications include chronic renal failure and nephrotic syndrome. After a few years, [[renal amyloidosis]] eventually leads to end stage renal disease and it may be accelerated by some factors such as steroid administration, [[renal vein thrombosis]], [[Infection|infections]] and [[surgery]]. | |||
==Diagnosis== | ==Diagnosis== | ||
===Diagnostic Study of Choice=== | ===Diagnostic Study of Choice=== | ||
Renal biopsy is the gold standard test for the diagnosis of [[Renal amyloidosis|renal diagnosis]] | |||
===History and Symptoms=== | ===History and Symptoms=== | ||
The majority of patients with renal amyloidosis have [[proteinuria]]. [[Swelling]] is very common in lower limbs. [[Numbness]] or tingling in hands or feet ([[carpal tunnel syndrome]]) is a less common finding. | |||
===Physical Examination=== | ===Physical Examination=== | ||
Physical examination of patients with [[renal amyloidosis]] is usually remarkable for [[swelling]], [[hepatosplenomegaly]], facial or neck [[purpura]] and [[macroglossia]]. Fatigue and unintentional [[weight loss]], are common in patients with AL [[amyloidosis]]. [[Tachycardia]]/[[bradycardia]] depends on the accompanying [[complication]]. Pulmonary fine [[crackles]], faint pulmonary auscultation, suggestive of [[pleural effusion]], decreased [[tactile fremitus]] and dull percussion. | |||
===Laboratory Findings=== | ===Laboratory Findings=== | ||
In patients with secondary [[amyloidosis]], [[urinalysis]] should be routinely examined. Laboratory findings consistent with the diagnosis of [[renal amyloidosis]] include [[proteinuria]] and increased serum [[creatinine]] | |||
===Electrocardiogram=== | ===Electrocardiogram=== | ||
There are no ECG findings associated with [[renal amyloidosis]]. | |||
===X-ray=== | ===X-ray=== | ||
There are no definitive findings on x-ray associated with [[renal amyloidosis]]. | |||
===Echocardiography and Ultrasound=== | ===Echocardiography and Ultrasound=== | ||
There are no echocardiography/ultrasound findings associated with [[renal amyloidosis]] | |||
===CT scan=== | ===CT scan=== | ||
There are no CT scan findings associated with [[renal amyloidosis]] | |||
===MRI=== | ===MRI=== | ||
There are no MRI findings associated with [[renal amyloidosis]]. | |||
===Other Imaging Findings=== | ===Other Imaging Findings=== | ||
There are no other imaging findings associated with [[renal amyloidosis]] | |||
===Other Diagnostic Studies=== | ===Other Diagnostic Studies=== | ||
Kidney biopsy can represent amyloid deposition as [[vascular]], [[tubulo-interstitial]] and/or [[glomerular]] deposits. All types of [[amyloidogenic]] proteins show affinity for Congo red dye. | |||
==Treatment== | ==Treatment== | ||
===Medical Therapy=== | ===Medical Therapy=== | ||
The mainstay of treatment for renal amyloidosis is to decrease the production or increase clearing of [[amyloid]]. Pharmacologic medical therapies for renal amyloidosis include [[colchicine]], [[azathioprine]], [[Dimethyl sulfoxide|dimethylsulfoxide]], [[chlorambucil]], [[methotrexate]], [[cyclophosphamide]] and TNF-alpha antagonists (ie, [[etanercept]], [[infliximab]], and [[adalimumab]]). | |||
===Surgery=== | ===Surgery=== | ||
In [[renal amyloidosis]], [[surgery]] is usually reserved for patients developed with end stage renal disease. The patients with [[renal amyloidosis]] are good candidates for transplantation. In primary amyloidosis, [[Kidney transplantation|renal transplantation]] is considered and it will improve long-term survival and quality of life. | |||
===Primary Prevention=== | ===Primary Prevention=== | ||
There are no established measures for the primary prevention of [[renal amyloidosis]]. | |||
===Secondary Prevention=== | ===Secondary Prevention=== | ||
Treatment of the primary disease and underlying cause will provide favorable renal outcome.{{WikiDoc Help Menu}} | |||
{{WikiDoc Help Menu}} | |||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category: (name of the system)]] | [[Category: (name of the system)]] | ||
Latest revision as of 18:32, 8 August 2018
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Renal amyloidosis Microchapters |
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Template:Renal amyloidosis On the Web |
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American Roentgen Ray Society Images of Renal amyloidosis overview |
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Risk calculators and risk factors for Renal amyloidosis overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Omer Kamal, M.D. [2]
Overview
Nicolaus Fontanus was the first to describe amyloidosis based on the result of an autopsy while Rudolph Virchow was the first to introduce the term amyloidosis. Renal amyloidosis can be classified according to the site of amyloid deposition into glomerular, vascular, and tubular amyloidosis. Suggested mechanisms of renal involvement include abnormal protein production or hereditary mutation. If left untreated, renal amyloidosis may progress into end stage renal disease. Common complications include chronic renal failure and nephrotic syndrome. After a few years, renal amyloidosis eventually leads to end stage renal disease and it may be progressed in presence of certain factors such as steroid administration, renal vein thrombosis, infections and surgery. There is insufficient evidence to recommend routine screening for renal amyloidosis. Renal biopsy is the gold standard test for the diagnosis of renal diagnosis. The mainstay of treatment for renal amyloidosis is to decrease the production or increase clearing of amyloid. Pharmacologic medical therapies for renal amyloidosis include colchicine, azathioprine, dimethylsulfoxide, chlorambucil, methotrexate, cyclophosphamide and TNF-alpha antagonists (ie, etanercept, infliximab, and adalimumab).
Historical Perspective
Nicolaus Fontanus was the first to describe amyloidosis based on the result of an autopsy while Rudolph Virchow was the first to introduce the term amyloidosis.
Classification
Renal amyloidosis can be classified according to the site of amyloid deposition into glomerular, vascular, and tubular amyloidosis.
Pathophysiology
Suggested mechanisms of renal involvement include abnormal protein production or hereditary mutation.
Causes
Most common causes of renal amyloidosis include primary and secondary amyloidosis. Other causes include transthyretin and fibrinogen amyloid deposition.
Differentiating Renal amyloidosis from Other Diseases
Epidemiology and Demographics
The incidence is 97 to 140 cases per 100,000 individuals. The incidence of renal amyloidosis increases with age; the median age at diagnosis is 65 years.
Risk Factors
Common risk factors in the development of renal amyloidosis may be environmental and genetic such as heterozygous mutations in the genes for lysozyme, apolipoprotein AI, apolipoprotein AII, or fibrinogen A alpha-chain.
Screening
There is insufficient evidence to recommend routine screening for renal amyloidosis.
Natural History, Complications, and Prognosis
If left untreated, renal amyloidosis may progress into end stage renal disease. Common complications include chronic renal failure and nephrotic syndrome. After a few years, renal amyloidosis eventually leads to end stage renal disease and it may be accelerated by some factors such as steroid administration, renal vein thrombosis, infections and surgery.
Diagnosis
Diagnostic Study of Choice
Renal biopsy is the gold standard test for the diagnosis of renal diagnosis
History and Symptoms
The majority of patients with renal amyloidosis have proteinuria. Swelling is very common in lower limbs. Numbness or tingling in hands or feet (carpal tunnel syndrome) is a less common finding.
Physical Examination
Physical examination of patients with renal amyloidosis is usually remarkable for swelling, hepatosplenomegaly, facial or neck purpura and macroglossia. Fatigue and unintentional weight loss, are common in patients with AL amyloidosis. Tachycardia/bradycardia depends on the accompanying complication. Pulmonary fine crackles, faint pulmonary auscultation, suggestive of pleural effusion, decreased tactile fremitus and dull percussion.
Laboratory Findings
In patients with secondary amyloidosis, urinalysis should be routinely examined. Laboratory findings consistent with the diagnosis of renal amyloidosis include proteinuria and increased serum creatinine
Electrocardiogram
There are no ECG findings associated with renal amyloidosis.
X-ray
There are no definitive findings on x-ray associated with renal amyloidosis.
Echocardiography and Ultrasound
There are no echocardiography/ultrasound findings associated with renal amyloidosis
CT scan
There are no CT scan findings associated with renal amyloidosis
MRI
There are no MRI findings associated with renal amyloidosis.
Other Imaging Findings
There are no other imaging findings associated with renal amyloidosis
Other Diagnostic Studies
Kidney biopsy can represent amyloid deposition as vascular, tubulo-interstitial and/or glomerular deposits. All types of amyloidogenic proteins show affinity for Congo red dye.
Treatment
Medical Therapy
The mainstay of treatment for renal amyloidosis is to decrease the production or increase clearing of amyloid. Pharmacologic medical therapies for renal amyloidosis include colchicine, azathioprine, dimethylsulfoxide, chlorambucil, methotrexate, cyclophosphamide and TNF-alpha antagonists (ie, etanercept, infliximab, and adalimumab).
Surgery
In renal amyloidosis, surgery is usually reserved for patients developed with end stage renal disease. The patients with renal amyloidosis are good candidates for transplantation. In primary amyloidosis, renal transplantation is considered and it will improve long-term survival and quality of life.
Primary Prevention
There are no established measures for the primary prevention of renal amyloidosis.
Secondary Prevention
Treatment of the primary disease and underlying cause will provide favorable renal outcome. Template:WikiDoc Sources