Wegener's granulomatosis: Difference between revisions
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{{ICD10 category|Heme/immunology}} | {{ICD10 category|Heme/immunology}}{{ICD10 category|Vasculitis}}{{ICD10 category|ANCA-associated Vasculitis (AAV)}} | ||
== Additional Info == | == Additional Info == | ||
Wegener's granulomatosis is also | *Wegener's granulomatosis is the OLD name of this disorder. | ||
*The new official name is Granulomatosis with polyangiitis (GPA) | |||
**It also is referred to as 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. | |||
*It is an autoimmune vasculitis, which causes inflammation and narrowing/blocking of small and medium-sized vessels. | |||
**This can occur in any organ(s) but most commonly affects the lungs and kidneys -- which can result in a "pulmonary-renal syndrome". Indeed it, along with '''[[Goodpasture syndrome (hypersensitivity angiitis)]]''' are the two most common specific causes of [[Pulmonary-Renal Syndrome in ICD10 | pulmonary-renal syndrome]]s. | |||
== 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 11:01, 28 May 2024
| ICD10 Diagnosis | |
| Dx: | Wegener's granulomatosis |
| ICD10 code: | M31.3 |
| Pre-ICD10 counterpart: | Wegener's Granulomatosis / Granulomatosis with polyangiitis |
| Charlson/ALERT Scale: | none |
| APACHE Como Component: | none |
| APACHE Acute Component: | none |
| Start Date: | |
| Stop Date: | |
| External ICD10 Documentation | |
This diagnosis is a part of ICD10 collection.
Additional Info
- Wegener's granulomatosis is the OLD name of this disorder.
- The new official name is Granulomatosis with polyangiitis (GPA)
- It also is referred to as 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.
- It is an autoimmune vasculitis, which causes inflammation and narrowing/blocking of small and medium-sized vessels.
- This can occur in any organ(s) but most commonly affects the lungs and kidneys -- which can result in a "pulmonary-renal syndrome". Indeed it, along with Goodpasture syndrome (hypersensitivity angiitis) are the two most common specific causes of pulmonary-renal syndromes.
Alternate ICD10s to consider coding instead or in addition
more specifically:
| ANCA-associated Vasculitis (AAV) codes: |
more generally:
| Vasculitis codes: |
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
| Related articles: |
Show all ICD10 Subcategories