Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis): Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
| (18 intermediate revisions by 5 users not shown) | |||
| Line 1: | Line 1: | ||
{{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. | *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. '''ANCA Serotype: Can be associated with either P-ANCA (primarily MPO-ANCA) or can be ANCA-negative.''' | ||
*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. The clinical presentations of these subtypes can overlap, making accurate diagnosis challenging. | |||
== Alternate ICD10s to consider coding instead or in addition == | == 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]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||
Latest revision as of 08:49, 8 June 2025
| 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: | |
| Data Dependencies(Reports/Indicators/Data Elements): | No results |
| 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. ANCA Serotype: Can be associated with either P-ANCA (primarily MPO-ANCA) or can be ANCA-negative.
- 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. The clinical presentations of these subtypes can overlap, making accurate diagnosis challenging.
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