Nephrotic syndrome classification: Difference between revisions

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Latest revision as of 22:57, 29 July 2020

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1], Ali Poyan Mehr, M.D. [2]; Associate Editor(s)-in-Chief: Olufunmilola Olubukola M.D.[3], Yazan Daaboul, Serge Korjian

Overview

Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology. Primary (idiopathic) nephrotic syndrome is defined as nephrotic syndrome due to a primary glomerular disease. The secondary nephrotic syndrome is defined as nephrotic syndrome due to a primary etiology other than glomerular disorders, such as infections, malignancies, systemic conditions, and medications.

Classification

Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.^[1]

Nephrotic
syndrome

Primary

Secondary

Below table lists different types of nephrotic syndromes:^[2]^[3]^[4]

Different types of nephrotic syndromes	Disease name
Podocytopathies	Primary	Minimal change disease
	Primary	Focal segmental glomerulosclerosis (FSGS)
	Secondary	Infection such as: HIV
		Drugs/toxins such as: NSAIDs Interferon Pamidronate Lithium Vaccins Envenomation
		Malignancies such as: Hodgkin lymphoma Thymoma
		Genetic disorders such as: Nephrin mutations Podocin gene mutations
Membranous glomerulonephritis	Primary	Membranous nephropathy
Membranous glomerulonephritis	Secondary	Drugs Toxins Malignancies
Membranoproliferative glomerulonephritis	Secondary	Autoimmune disorders such as: SLE Aquired C3 glomerulopathy Infections such as: HCV Endocarditis Genetics Malignancies Thrombotic microangiopathy
Hereditary Nephropathy	Alport syndrome IgA nephropathy C1q nephropathy
Glomerular deposition diseases	Diabetes mellitus Amyloidosis Monoclonal deposition disease Nodular glomeruloneohritis associated with heavy smoking
Others	Fabry disease Nail-patella syndrome Partial lipodystrophy Preeclampsia

References

↑ Kodner C (2009). "Nephrotic syndrome in adults: diagnosis and management". Am Fam Physician. 80 (10): 1129–34. PMID 19904897.
↑ Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ (May 2000). "Changing incidence of glomerular diseases in adults". Am. J. Kidney Dis. 35 (5): 878–83. PMID 10793022.
↑ Heaf J (September 2004). "The Danish Renal Biopsy Register". Kidney Int. 66 (3): 895–7. doi:10.1111/j.1523-1755.2004.00832.x. PMID 15327377.
↑ Ha TS (March 2017). "Genetics of hereditary nephrotic syndrome: a clinical review". Korean J Pediatr. 60 (3): 55–63. doi:10.3345/kjp.2017.60.3.55. PMC 5383633. PMID 28392820.

[pmid19904897-1] Kodner C (2009). "Nephrotic syndrome in adults: diagnosis and management". Am Fam Physician. 80 (10): 1129–34. PMID 19904897.

[pmid10793022-2] Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ (May 2000). "Changing incidence of glomerular diseases in adults". Am. J. Kidney Dis. 35 (5): 878–83. PMID 10793022.

[pmid15327377-3] Heaf J (September 2004). "The Danish Renal Biopsy Register". Kidney Int. 66 (3): 895–7. doi:10.1111/j.1523-1755.2004.00832.x. PMID 15327377.

[pmid28392820-4] Ha TS (March 2017). "Genetics of hereditary nephrotic syndrome: a clinical review". Korean J Pediatr. 60 (3): 55–63. doi:10.3345/kjp.2017.60.3.55. PMC 5383633. PMID 28392820.

[1]

[2]

[3]

[4]

@@ Line 1: / Line 1: @@
 __NOTOC__
 {{Nephrotic syndrome}}
-{{CMG}} {{APM}}; {{AE}} {{OO}} [[User:YazanDaaboul|Yazan Daaboul]],
+{{CMG}}, {{APM}}; {{AE}} {{OO}}, [[User:YazanDaaboul|Yazan Daaboul]], [[User:Sergekorjian|Serge Korjian]]
-[[User:Sergekorjian|Serge Korjian]]
 ==Overview==
-Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.  Primary (idiopathic) nephrotic syndrome is defined as nephrotic syndrome due to a primary [[glomerular]] disease.  Secondary nephrotic syndrome is defined as nephrotic syndrome due to a primary etiology other than glomerular disorders, such as [[infection]]s, [[malignancies]], systemic conditions, and [[medication]]s.
+Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.  Primary (idiopathic) nephrotic syndrome is defined as nephrotic syndrome due to a primary [[glomerular]] disease. The secondary nephrotic syndrome is defined as nephrotic syndrome due to a primary etiology other than glomerular disorders, such as [[infection]]s, [[malignancies]], systemic conditions, and [[medication]]s.
 ==Classification==
-===Etiologic Classification===
+* Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.<ref name="pmid19904897">{{cite journal| author=Kodner C| title=Nephrotic syndrome in adults: diagnosis and management. | journal=Am Fam Physician | year= 2009 | volume= 80 | issue= 10 | pages= 1129-34 | pmid=19904897 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19904897 }} </ref>
-Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.<ref name="pmid19904897">{{cite journal| author=Kodner C| title=Nephrotic syndrome in adults: diagnosis and management. | journal=Am Fam Physician | year= 2009 | volume= 80 | issue= 10 | pages= 1129-34 | pmid=19904897 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19904897 }} </ref>
 <center>
 {{familytree/start}}
@@ Line 18: / Line 15: @@
 {{familytree/end}}
 </center>
-Below table lists different typesof nephrotic syndromes:
+* Below table lists different types of nephrotic syndromes:<ref name="pmid10793022">{{cite journal |vauthors=Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ |title=Changing incidence of glomerular diseases in adults |journal=Am. J. Kidney Dis. |volume=35 |issue=5 |pages=878–83 |date=May 2000 |pmid=10793022 |doi= |url=}}</ref><ref name="pmid15327377">{{cite journal |vauthors=Heaf J |title=The Danish Renal Biopsy Register |journal=Kidney Int. |volume=66 |issue=3 |pages=895–7 |date=September 2004 |pmid=15327377 |doi=10.1111/j.1523-1755.2004.00832.x |url=}}</ref><ref name="pmid28392820">{{cite journal |vauthors=Ha TS |title=Genetics of hereditary nephrotic syndrome: a clinical review |journal=Korean J Pediatr |volume=60 |issue=3 |pages=55–63 |date=March 2017 |pmid=28392820 |pmc=5383633 |doi=10.3345/kjp.2017.60.3.55 |url=}}</ref>
-{| class="wikitable"
+{|
-!Different types of nephrotic syndromes
+! align="center" style="background:#4479BA; color: #FFFFFF;" + |Different types of nephrotic syndromes
-! colspan="2" |Disease name
+! colspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Disease name
 |-
-| rowspan="6" |Podocytopathies
+! rowspan="6" align="center" style="background:#DCDCDC;" + |Podocytopathies
-| rowspan="2" |Primary
+| rowspan="2" align="left" style="background:#F5F5F5;" + |Primary
-|Primary [[minimal change disease]]
+| align="left" style="background:#F5F5F5;" + |[[Minimal change disease]]
 |-
-|Primary [[Focal segmental glomerulosclerosis|FSGS]]
+| align="left" style="background:#F5F5F5;" + |[[Focal segmental glomerulosclerosis]] ([[Focal segmental glomerulosclerosis|FSGS]])
 |-
-| rowspan="4" |Secondary
+| rowspan="4" align="left" style="background:#F5F5F5;" + |Secondary
-|Infection: [[Human Immunodeficiency Virus (HIV)|HIV]]
+| align="left" style="background:#F5F5F5;" + |Infection such as:
+* [[Human Immunodeficiency Virus (HIV)|HIV]]
 |-
-|Drugs/toxins: [[Non-steroidal anti-inflammatory drug|NSAIDs]], [[interferon]], [[pamidronate]], [[lithium]], [[Vaccination|vaccins]], [[envenomation]]
+| align="left" style="background:#F5F5F5;" + |Drugs/toxins such as:
+* [[Non-steroidal anti-inflammatory drug|NSAIDs]]
+* Interferon
+* Pamidronate
+* Lithium
+* Vaccins
+* Envenomation
 |-
-|Malignancies: [[Hodgkin's lymphoma|hodgkin lymphoma]], [[thymoma]]
+| align="left" style="background:#F5F5F5;" + |Malignancies such as:
+* [[Hodgkin's lymphoma|Hodgkin lymphoma]]
+* [[Thymoma]]
 |-
-|Genetics: [[nephrin]] mutations, [[podocin]]
+| align="left" style="background:#F5F5F5;" + |Genetic disorders such as:
+* [[Nephrin]] mutations
+* [[Podocin]] gene mutations
 |-
-| rowspan="2" |[[Membranous glomerulonephritis]]
+! rowspan="2" align="center" style="background:#DCDCDC;" + |[[Membranous glomerulonephritis]]
-|Primary
+| align="left" style="background:#F5F5F5;" + |Primary
-|Primary [[membranous nephropathy]]
+| align="left" style="background:#F5F5F5;" + |[[Membranous nephritis|Membranous nephropathy]]
 |-
-|Secondary
+| align="left" style="background:#F5F5F5;" + |Secondary
-|Drugs, [[Toxin|toxins]], [[malignancies]]
+| align="left" style="background:#F5F5F5;" + |
+* [[Drugs]]
+* [[Toxin|Toxins]]
+* [[Cancer|Malignancies]]
 |-
-|[[Membranoproliferative glomerulonephritis]]
+! align="center" style="background:#DCDCDC;" + |[[Membranoproliferative glomerulonephritis]]
-|Secondary
+| align="left" style="background:#F5F5F5;" + |Secondary
-|
+| align="left" style="background:#F5F5F5;" + |
-* Autoimmune disorders: [[SLE]], aquired C3 glomerulopathy
+* Autoimmune disorders such as:
-* Infections: [[Hepatitis C|HCV]], [[endocarditis]]
+** [[SLE]]
+** Aquired [[C3 glomerulopathy]]
+* Infections such as:
+** [[Hepatitis C|HCV]]
+** [[Endocarditis]]
 * [[Genetics]]
 * [[Malignancies]]
 * [[Thrombotic microangiopathy]]
 |-
-|Glomerular deposition diseases
+! align="center" style="background:#DCDCDC;" + |Hereditary Nephropathy
-| colspan="2" |
+| colspan="2" align="left" style="background:#F5F5F5;" + |
+* [[Alport syndrome]]
+* [[IgA nephropathy]]
+* C1q nephropathy
+|-
+! align="center" style="background:#DCDCDC;" + |[[Glomerular deposition disease|Glomerular deposition diseases]]
+| colspan="2" align="left" style="background:#F5F5F5;" + |
 * [[Diabetes mellitus]]
 * [[Amyloidosis]]
 * [[Monoclonal antibodies|Monoclonal]] deposition disease
-* Nodular glomeruloneohritis associated with heavy smoking
+* Nodular glomeruloneohritis associated with heavy [[smoking]]
 |-
-|Other lesions
+! align="center" style="background:#DCDCDC;" + |Others
-| colspan="2" |
+| colspan="2" align="left" style="background:#F5F5F5;" + |
-* [[Alport syndrome]]
 * [[Fabry's disease|Fabry disease]]
 * [[Nail-patella syndrome]]
@@ Line 69: / Line 89: @@
 * [[Pre-eclampsia|Preeclampsia]]
 |}
-*Hereditary Nephropathies: are group of disorders that present with both the features of nephrotic and nephritic syndromes. When features of nephritic syndrome are associated with sensorineural deafness, it is called Alport’s syndrome. Other hereditary nephropathies include IgA Nephropathy, C1q Nephropathy, etc.
 ==References==
 {{Reflist|2}}
-[[Category:Kidney diseases]]
+[[Category:Medicine]]
 [[Category:Nephrology]]
-[[Category:Pediatrics]]
+[[Category:Urology]]
-[[Category:Disease]]
+[[Category:Up-To-Date]]
-[[Category:Syndromes]]
+[[Category:Emergency medicine]]
-[[Category:Needs overview]]
-[[Category:Primary care]]
-{{WH}}
-{{WS}}

Nephrotic syndrome classification: Difference between revisions

Latest revision as of 22:57, 29 July 2020

Overview

Classification

References

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