Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis): Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Churg-Strauss Syndrome| CurrentStatus = | | OldDxArticle =Churg-Strauss Syndrome | ||
| CurrentStatus = reconciled | |||
| InitialEditorAssigned = Marla Penner | | InitialEditorAssigned = Marla Penner | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=M30.1 | | ICD10 Code=M30.1 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Heme/immunology}}, {{ICD10 category|Allergy}}, {{ICD10 category|Allergy}} | |||
{{ICD10 category| | {{ICD10 category|Vasculitis}}{{ICD10 category|ANCA-associated Vasculitis (AAV)}} | ||
== Additional Info == | == Additional Info == | ||
*Churg-Strauss syndrome, now also referred to by its medically more accurate term eosinophilic granulomatosis with polyangiitis (EGPA), is a rare systemic vasculitis (inflammation in the wall of blood vessels of the body), predominantly affecting small-sized vessels. | |||
*This is considered to be an ANCA-associated Vasculitis (AAV)- 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. | |||
== Alternate ICD10s to consider coding instead or in addition == | |||
more specifically: | |||
{{ListICD10Category | categoryName = ANCA-associated Vasculitis (AAV)}} | |||
= | more generally: | ||
{{ListICD10Category | categoryName = Vasculitis}} | |||
== Candidate [[Combined ICD10 codes]] == | |||
== | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | |||
{{ICD10 footer}} | |||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||
Latest revision as of 11:03, 2024 May 28
ICD10 Diagnosis | |
Dx: | Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis) |
ICD10 code: | M30.1 |
Pre-ICD10 counterpart: | Churg-Strauss Syndrome |
Charlson/ALERT Scale: | none |
APACHE Como Component: | none |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
, ,Additional Info
- Churg-Strauss syndrome, now also referred to by its medically more accurate term eosinophilic granulomatosis with polyangiitis (EGPA), is a rare systemic vasculitis (inflammation in the wall of blood vessels of the body), predominantly affecting small-sized vessels.
- This is considered to be an ANCA-associated Vasculitis (AAV)- 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.
Alternate ICD10s to consider coding instead or in addition
more specifically:
ANCA-associated Vasculitis (AAV) codes: |
more generally:
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
Show all ICD10 Subcategories