Verruga peruana
Synonyms: Peruvian warts
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
A rare bacterial infectious disease characterized by development of endothelial cell-derived, blood-filled tumors on the surface of the skin during the chronic phase of infection with <i>Bartonella bacilliformis</i>. The lesions can persist for months to years and may cause pain and scarring due to ulceration. They are classified as miliary (multiple red papules of <3 mm in diameter), mular (blood-filled nodules), and diffuse (groups of subdermal nodules >5 mm in diameter). Eruptions may be accompanied by fever and malaise, lymphadenopathy, acute bone and joint pains, and headache. Fatality rates during this phase are low.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Verruga peruana | Peruvian warts |
| fr | Verruga péruvienne | Verrue de Carrion · Verruga du Pérou · Verruga peruana |
| de | Verruga peruana | Peruanische Warze |
| es | Verruga peruana | |
| it | Verruca peruviana | Verruche peruviane |
| nl | Verruga peruana | Peruviaanse wratten |
| pt | Verruga peruana | Verrugas peruanas |
| pl | Brodawczakowatość peruwiańska | = en |
| cs | Verruga peruana | = en |
| uk | Системний бартонельоз | Перуанські бородавки |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A44.1 | NTBT | inclusion | validated |
| ICD-11 | 1C11.01 | E | specific | validated |
| MONDO | 0971058 | E | validated | |
| UMLS | C0042552 | E | validated | |
| MedDRA | 10080438 | 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:64692Bartonella bacilliformis infection
rare infectious diseases
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/659759
- This record as JSON: /data/d/659759.json