Microscopic polyangiitis/polyarteritis: Difference between revisions

Mpenner (talk | contribs)
No edit summary
m moved Polyarteritis nodosa (PAN) to that article, not sure why it was here.
Line 1: Line 1:
{{ICD10 transition status
{{ICD10 transition status
| OldDxArticle =| CurrentStatus = reconciled  
| OldDxArticle =
| CurrentStatus = reconciled  
| InitialEditorAssigned = Marla Penner
| InitialEditorAssigned = Marla Penner
| MinimumCombinedCodes =
| MinimumCombinedCodes =
Line 9: Line 9:
| BugRequired=  
| BugRequired=  
}}
}}
{{ICD10 category|Heme/immunology}}{{ICD10 category|Cardiovascular}} 


{{ICD10 category|Heme/immunology}}
== Additional Info ==
== 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.
*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.


== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
Line 20: Line 19:


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==
(put links to likely candidates coded with this one, eg. a cause for a trauma.)
 


== Related Articles ==
== Related Articles ==