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 = reconciled | | 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}} | ||
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