Polyarteritis Nodosa: ['A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative. [ NCI ]']
| Name | M13_POYARTOTH |
|---|---|
| Long name | Other conditions related to polyarteritis nodosa |
| Hospital Discharge registry | ICD-10: M308, ICD-9: 4460C |
| Cause of Death registry | ICD-10: M308, ICD-9: 4460C |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
| Latin name | Aliae condiciones polyarteritidi nodosae cognatae |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 28 | 20 | 8 |
| Unadjusted prevalence (%) | 0.01 | 0.02 | 0.01 |
| Mean age at first event (years) | 53.00 | 49.63 | 61.43 |
| Case fatality at 5-years (%) | 0.00 | 0.00 | 0.00 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 1.5 | 1.0 | 3.5 |
| Recurrence at 6 months (%) | 42.86 | 35.00 | 62.50 |
before Other conditions related to polyarteritis nodosa
after Other conditions related to polyarteritis nodosa
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