Drug-induced vasculitis
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare secondary vasculitis characterized by inflammation of blood vessels caused by various drugs, including antibiotics, anti-tumor necrosis factor-alpha agents, immunotherapeutic drugs, and psychoactive agents, among others. The skin is most commonly affected, but other tissues and organs, such as the subcutis, kidneys, or lungs, may also be involved. Systemic disease develops only in a minority of patients, typically when treated with the causative drug over a prolonged period of time. Presenting signs and symptoms include skin rash, myalgia, arthralgia, fever, and malaise.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Drug-induced vasculitis | |
| fr | Vascularite induite par les médicaments | |
| de | Vaskulitis, Medikamenten-induzierte | |
| es | Vasculitis inducida por fármacos | Vasculitis inducida por medicamentos |
| it | Vasculite indotta da farmaci | |
| nl | Medicatiegeïnduceerde vasculitis | |
| pt | Vasculite induzida por fármacos | |
| pl | Zapalenie naczyń indukowane lekami | |
| cs | Léky indukovaná vaskulitida | |
| uk | Медикаментозний васкуліт | |
| zh | 药物性血管炎 | |
| tr | İlaca bağlı vaskülit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M31.8 | NTBT | attributed | validated |
| ICD-11 | 4A85.03 | E | specific | validated |
| MONDO | 0016664 | E | validated | |
| UMLS | C0340672 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:445197Secondary vasculitis
rare systemic and rheumatological diseases; rare circulatory system diseases; rare systemic or rheumatologic diseases of childhood
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/251325
- This record as JSON: /data/d/251325.json