Microscopic polyangiitis/polyarteritis: Difference between revisions

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{{ICD10 transition status

| OldDxArticle =| CurrentStatus = ~~manually added for testing~~

| OldDxArticle =

| CurrentStatus = reconciled

| InitialEditorAssigned = Marla Penner

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{{ICD10 dx

| MinimumCombinedCodes =

| ICD10 Code=M31.7

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{{ICD10 category|Heme/immunology}}{{ICD10 category|Cardiovascular}}{{ICD10 category|Vasculitis}}{{ICD10 category|ANCA-associated Vasculitis (AAV)}}

== Additional Info ==

{~~sc:polyarteritis nosoda~~}

*Microscopic polyangiitis (MPA) is a vasculitis of small vessels. Patients frequently present with renal manifestations, but systemic manifestations, arthritis, mononeuritis multiplex, and other signs and symptoms are also common.

*It is considered to be an ANCA-associated Vasculitis (AAV)- '''ANCA Serotype: Primarily associated with P-ANCA, which recognizes myeloperoxidase (MPO).'''

Antineutrophilic cytoplasmic antibody (ANCA) associated vasculitides are a heterogeneous group of rare autoimmune conditions that causes an inflammation of blood vessels with various manifestations. It includes three main diseases, which are granulomatosis with polyangiitis (GPA; formerly known as Wegener granulomatosis), eosinophilic granulomatosis with polyangiitis (EGPA; previously known as Churg-Strauss syndrome), and microscopic polyangiitis (MPA). Other ANCA-associated diseases are drug-induced vasculitis and renal limited vasculitis. The clinical presentations of these subtypes can overlap, making accurate diagnosis challenging.

== Alternate ICD10s to consider coding instead or in addition ==

*[[Polyarteritis nodosa (PAN)]]

more specifically:

{{ListICD10Category | categoryName = ANCA-associated Vasculitis (AAV)}}

~~== Alternate ICD10s to consider coding instead ==~~

more generally:

~~(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)~~

{~~sc:polyarteritis nosoda~~}

== Candidate [[Combined ICD10 codes]] ==

~~(put links to likely candidates coded with this one, eg. a cause for a trauma.)~~

== Related CCI Codes ==

== Related Articles ==

@@ Line 1: / Line 1: @@
 {{ICD10 transition status
-| OldDxArticle =| CurrentStatus = manually added for testing
+| OldDxArticle =
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Marla Penner
-| MinimumCombinedCodes =
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=M31.7
 | BugRequired=
 }}
+{{ICD10 category|Heme/immunology}}{{ICD10 category|Cardiovascular}}{{ICD10 category|Vasculitis}}{{ICD10 category|ANCA-associated Vasculitis (AAV)}}
 == Additional Info ==
-{sc:polyarteritis nosoda}
+*Microscopic polyangiitis (MPA) is a vasculitis of small vessels. Patients frequently present with renal manifestations, but systemic manifestations, arthritis, mononeuritis multiplex, and other signs and symptoms are also common.
+*It is considered to be an ANCA-associated Vasculitis (AAV)- '''ANCA Serotype: Primarily associated with P-ANCA, which recognizes myeloperoxidase (MPO).'''
+Antineutrophilic cytoplasmic antibody (ANCA) associated vasculitides are a heterogeneous group of rare autoimmune conditions that causes an inflammation of blood vessels with various manifestations. It includes three main diseases, which are granulomatosis with polyangiitis (GPA; formerly known as Wegener granulomatosis), eosinophilic granulomatosis with polyangiitis (EGPA; previously known as Churg-Strauss syndrome), and microscopic polyangiitis (MPA). Other ANCA-associated diseases are drug-induced vasculitis and renal limited vasculitis.  The clinical presentations of these subtypes can overlap, making accurate diagnosis challenging.
+== Alternate ICD10s to consider coding instead or in addition ==
+*[[Polyarteritis nodosa (PAN)]]
+more specifically:
+{{ListICD10Category | categoryName = ANCA-associated Vasculitis (AAV)}}
-== Alternate ICD10s to consider coding instead ==
+more generally:
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+{{ListICD10Category | categoryName = Vasculitis}}
-{sc:polyarteritis nosoda}
 == Candidate [[Combined ICD10 codes]] ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
+== Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}