Microscopic polyangiitis/polyarteritis: Difference between revisions

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{{ICD10 transition status

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| CurrentStatus = reconciled

| InitialEditorAssigned = Marla Penner

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{{ICD10 dx

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| ICD10 Code=M31.7

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

~~{{ICD10 category|Heme/immunology}}~~

== Additional Info ==

*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.

*~~Polyarteritis nodosa~~ (~~PAN~~) is a rare ~~disease~~ that ~~results from~~ blood ~~vessel inflammation~~ ("vasculitis~~") causing injury to organ systems~~. The ~~areas most commonly affected by PAN include the nerves~~, ~~intestinal tract, heart, and joints~~.

*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)]]

*[[Primary Systemic Vasculitis]]

more specifically:

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

more generally:

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

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

== Related CCI Codes ==

== Related Articles ==

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 {{ICD10 transition status
-| OldDxArticle =| CurrentStatus = reconciled
+| 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)}}
-{{ICD10 category|Heme/immunology}}
 == Additional Info ==
 *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.
-*Polyarteritis nodosa (PAN) is a rare disease that results from blood vessel inflammation ("vasculitis") causing injury to organ systems. The areas most commonly affected by PAN include the nerves, intestinal tract, heart, and joints.
+*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)]]
-*[[Primary Systemic Vasculitis]]
+more specifically:
+{{ListICD10Category | categoryName = ANCA-associated Vasculitis (AAV)}}
+more generally:
+{{ListICD10Category | categoryName = Vasculitis}}
 == 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}}
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