Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis): Difference between revisions
Ttenbergen (talk | contribs) m Text replacement - "Muscoloskeletal/soft" to "Musculoskeletal/soft" |
Ttenbergen (talk | contribs) should this really be in category Musculoskeletal/soft tissue? |
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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 | ||
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{{ICD10 category|Heme/immunology}} | |||
{{ | {{discussion}} should this really be in category Musculoskeletal/soft tissue? {{ICD10 category|Musculoskeletal/soft tissue}} | ||
== 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. | ||