Edit ICD10 dx: Microscopic polyangiitis/polyarteritis

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{{ICD10 transition status | OldDxArticle = | CurrentStatus = reconciled | InitialEditorAssigned = Marla Penner }} == 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. *It is considered to be an ANCA-associated Vasculitis (AAV)- '''ANCA Serotype: Primarily associated with P-ANCA, which recognizes myeloperoxidase (MPO).''' 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 == *[[Polyarteritis nodosa (PAN)]] 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}} {{ICD10 footer}} {{EndPlaceHolder}}

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